bone acidic glycoprotein-75 delineates the extracellular sites of
TRANSCRIPT
Bone Acidic Glycoprotein-75 Delineates the Extracellular Sites of Future Bone Sialoprotein
Accumulation and Apatite Nucleation in Osteoblastic Cultures1,2. Ronald J. Midura, Aimin Wang, Dinah Lovitch*, Douglas Law**, Kimerly Powell, and Jeff P. Gorski * Department of Biomedical Engineering and the Orthopaedic Research Center, Lerner Research Institute of The Cleveland Clinic and Foundation, Cleveland, OH; *Division of Biochemistry and Molecular Biology, School of Biological Sciences, and Department of Oral Biology, School of Dentistry, University of Missouri-Kansas City, Kansas City, MO, and **Division of Cell Biology and Biophysics, School of Biological Sciences, University of Missouri-Kansas City, Kansas City, MO Keywords: Bone acidic glycoprotein-75, bone sialoprotein, biomineralization, primary bone, hydroxyapatite, extracellular matrix Please address all correspondence to: Dr. Ronald J. Midura, Dept. Biomedical Engineering, ND20, The Cleveland Clinic Foundation, 9500 Euclid Ave., Cleveland, OH 44195 Phone: 216-445-3212 Fax: 216-445-4383 Email: [email protected]
JBC Papers in Press. Published on March 5, 2004 as Manuscript M312409200
Copyright 2004 by The American Society for Biochemistry and Molecular Biology, Inc.
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ABSTRACT
Addition of an organophosphate source to UMR osteoblastic cultures activates a mineralization
program in which BSP localizes to extracellular matrix sites where hydroxyapatite crystals are
subsequently nucleated (Wang, A., Martin, J.A., Lembke, L.A., and Midura, R.J. 2000.
Reversible Suppression of in vitro Biomineralization by Activation of Protein Kinase A. J. Biol.
Chem. 275:11082-11091). This study identifies for the first time novel extracellular spherical
structures, termed biomineralization foci (BMF), containing bone acidic glycoprotein-75 (BAG-
75), bone sialoprotein (BSP), and alkaline phosphatase that are the exclusive sites of initial
nucleation of hydroxyapatite crystals in the UMR model. Importantly, in the absence of added
phosphate, UMR cultures after reaching confluency contain two size populations of
morphologically identifiable BMF precursors enriched in BAG-75 (15-25 and 150-250 microns
in diameter). The shape and size of the smaller population are similar to structures assembled in
vitro through self-association of purified BAG-75 protein (Gorski, J.P., Kremer, E.A., Chen, Y.,
Ryan, S., Fullenkamp, C., Delviscio, J., Jensen, K., and McKee, M.D. 1997. Bone acidic
glycoprotein-75 self-associates to form macromolecular complexes in vitro and in vivo with the
potential to sequester phosphate ions. J. Cellular Biochem. 64:547-564). After organophosphate
addition, BSP accumulates within these BAG-75-containing BMF precursors, with
hydroxyapatite crystal nucleation occurring subsequently. In summary, BAG-75 is the earliest
detectable biomarker that accurately predicts the extracellular sites of de novo biomineralization
in UMR cultures. We hypothesize that BAG-75 may perform a key structural role in the
assembly of BMF precursors and the recruitment of other proteins such as alkaline phosphatase
and BSP. Furthermore, we propose a hypothetical mechanism in which BAG-75 and BSP
function actively in nucleation of apatite within BMF.
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Introduction
The mechanisms responsible for biomineralization of mammalian bone remain
unresolved (1-8). One theory proposes that biomineralization reactions are initiated within
phospholipid membrane-delimited vesicles (matrix vesicles) released into the extracellular
matrix by osteoblasts (1,3,5,8). Another proposes that mineralization is initiated within the “hole
zone” of collagen fibrils at the mineralization front of osteoid in a process requiring
noncollagenous phosphoproteins (1,2,4). In vitro studies have shown that some of these
phosphoproteins can nucleate the formation of apatite crystals when located within collagen or
agarose gels (6,9,10). However, most prior studies of biomineralization have not seriously
considered whether their models were consistent with the kinetics or spatial patterning with
which bone mineralizes in vivo.
Several noncollagenous bone matrix proteins are believed to play an active role in the
biochemical reactions involved in bone biomineralization. One of these proteins, bone
sialoprotein (BSP), is a sulfated, phosphorylated matrix glycoprotein containing an RGD integrin
receptor-binding site (11). BSP has been proposed to function as an apatite nucleator because it
is found in the mineralizing boundaries of bone, dentin and calcifying cartilage tissues (12-17)
co-localizing with the smallest detectable foci of newly forming mineralized matrix in osteoid
(18), and is expressed prior to and during the active mineralization periods of osteoblastic
cultures that produce apatite crystals of biological proportions (19,20). Furthermore, purified
BSP nucleates a small amount of apatite in vitro (9) likely mediated by its polyglutamate
domains (10,21).
Another noncollagenous bone matrix protein, bone acidic glycoprotein-75 (BAG-75), is an
acidic glycoprotein of 75 kDa in apparent size that contains elevated contents of Asp/Glu (29%),
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sialic acid, and covalently bound phosphate (44 res./mol) (22). Research to date indicates that
BAG-75 is restricted in its expression to actively forming primary or woven bone and dentin (23-
26). Purified BAG-75 displays a strong propensity to self-associate into supramolecular
spherical complexes (10-20 µm diameter) composed of 10-12 nm diameter microfibrils (24,27).
Electronegative complexes composed of BAG-75 can sequester millimolar quantities of
phosphate ions that are available for crystal nucleation reactions (24); BAG-75 also binds up to
135 atoms of Ca+2/molecule at saturation (28). Multimeric BAG-75 complexes exist in vivo at
sites of new primary bone formation as demonstrated by staining frozen tissue sections with a
BAG-75 aggregation-specific monoclonal antibody (24).
While conclusions from in vitro models require validation in vivo [see Gorski et al.,
companion paper (29)], culture systems are readily controlled and reproducible. The UMR 106-
01 BSP cell line constitutively expresses a mature osteoblastic phenotype and is able to deposit
ample amounts of apatite crystals within discrete focal sites over a 24 h incubation period after
addition of an organophosphate source (19,30). Several findings from our laboratory support the
physiological relevancy of the UMR culture model. Most notably, Wang et al. (30) have shown
that the biomineralization processes in both UMR and primary osteoblast cultures are similarly
regulated by parathyroid hormone treatment. Furthermore, the UMR biomineralization process
is an active metabolic process requiring continuous protein synthesis and secretion (19). Lastly,
X-ray diffraction analyses demonstrate that mineral crystals formed in mineralizing UMR
cultures are apatite and have a similar C-axis length as that of apatite crystals isolated from
pediatric bone samples (19). Altogether, our prior work indicates that UMR cultures deposit
apatite crystals at focal sites in a physiologically relevant manner.
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BSP quantitatively accumulates within biomineralization foci (BMF) only after treatment of
UMR cultures with organophosphates (30). BSP is first detected within BMF after 4-8 h, well
before the first appearance of apatite crystals within BMF (30). Thus, in this model system, BSP
fulfills the minimal necessary temporal-spatial requirements of a protein involved in apatite
nucleation. However, it is not known how BSP is targeted quantitatively to BMF. The present
study was undertaken to determine whether mineralizing UMR cultures, like initial sites of
mineral nucleation in primary bone [see Gorski et al., companion paper (29)], accumulate BSP
and then hydroxyapatite within BAG-75 containing BMF precursors.
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Materials and methods
Antibodies
The sources of antibodies used in the study were as follows: monoclonal anti-BSP, WV1D1
(9C5) antibody was obtained from the Developmental Studies Hybridoma Bank (Univ. of Iowa,
Iowa City, IA); anti-BAG-75 protein antibodies (#504) were provided by Jeff Gorski (23).
Monospecific polyclonal antiserum raised against rat BSP (LF-87) was obtained from Larry
Fisher (NICDR, NIH) (31). The 504 polyclonal antiserum for BAG-75 (23,24,26,27), and the
WVIDI (9C5) monoclonal antibody for BSP (30) have been shown to be monospecific in light
level immunolocalization, electron microscopic ultrastructural studies, and Western blot
analyses.
Cell culture and treatment with β-glycerophosphate
MC3T3-E1 (subclone M4) osteoblastic cells were cultured and treated with 5 mM β-
glycerophosphate (β-GP) as previously described (32,33). UMR 106-01 BSP cells were passaged
and cultured as described by Wang et al. (30). Prior to immunochemical analyses, cells were
seeded onto either 25 mm Aclar® 33 C .005 thick plastic cover slips (Allied Signal's medical
grade) in 6-well dishes or serum-coated Fisher Plus glass slides in petri dishes (both for confocal
analyses), or Permanox® tissue culture dishes (for electron microscopy analyses, Fisher
Scientific), at a density of 1000 cells/mm2 in growth medium [Eagles minimum essential
medium plus nonessential amino acids, 2 mM L-glutamine, 20 mM HEPES (pH 7.2), and 10%
fetal bovine serum]. At 64 h of incubation, the medium was replaced with fresh growth medium
for an additional 24 h (biomineralization period) supplemented with or without β-GP at a final
concentration of 7 mM. β-GP was prepared as sterile 0.7 M stocks in Nanopure water adjusted
to a final pH of 7.0; aliquots were added directly to fresh medium immediately before initiating
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biomineralization. Unless otherwise stated, cells were fixed by immersion in cold 70% ethanol
and stored as such at 4° C until processed further.
Wang et al. (30) have previously demonstrated that UMR cultures treated with as little as
1 nM parathyroid hormone expressed high alkaline phosphatase activity levels, and a near
complete conversion of β-GP into inorganic phosphate, yet did not precipitate calcium phosphate
crystals. Chang et al. (34) also reported that spontaneous crystallization of calcium and
phosphate did not occur in UMR culture medium even when the concentrations of these ions
were elevated. Therefore, chemical precipitation is not the primary mechanism governing
mineral formation in this model system.
Culture of fetal rat calvarial cells and treatment with β-GP
As described previously (35,36), calvaria were removed from 19-day fetal rats and sequentially
digested with 0.2% collagenase/0.05% trypsin in HBSS 6 times for 20 minutes each. The
supernatants from the first two digests were discarded and the supernatants from the remaining
digests, rich in osteoblast precursor cells, were pooled for culture. Cells were plated at 2-3 x 108
cells per T75 flasks in α-minimal essential media supplemented with glutamine and nucleosides
(Mediatech, Inc.), 10% FBS, and 0.5% penicillin/streptomycin (Pen/Strep) antibiotic. Cells were
grown to confluence (3-4 days), trypsinized and then plated for experiments in chamber slides at
8000 cells /chamber. After reaching confluency, first passage cultures were re-fed every three
days with medium supplemented with 5% FBS, 0.5% Pen/Strep, 100 µg/ml ascorbic acid, and
with 5 mM β-GP to promote the formation and mineralization of bone mineralization foci.
Controls did not receive ßGP. At 7 and 17 days after reaching confluence, culture slides were
fixed in 4% paraformaldehyde for 2.5 h at room temperature and were then stored 70% ethanol
at 4°C until stained with Alizarin red S.
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Visualization of apatite mineral using Alizarin red-S
After removal of medium, UMR cultures were briefly rinsed with TBS followed by fixation in
ice-cold 70% ethanol for 1 h. Fixed samples were washed three times with TBS, rinsed with de-
ionized water, and then stained for 10 min with either 40 mM or 0.4 mM Alizarin red-S dye, pH
4.2, at room temperature for brightfield (19) or epifluorescent microscopy (30), respectively.
Cultures were then rinsed five times with water followed by a 15 min wash with TBS to reduce
nonspecific AR-S stain. When necessary, fixed mineralized cultures were decalcified using one
of three methods: (1) treatment with Tris-buffered saline (pH 8.0) containing 50 mM EDTA
overnight at 4° C, (2) treatment with 10% trichloroacetic acid for 10 min. at 4° C, or (3)
treatment with 0.1 M HCl in 70% ethanol for 30 min. at 4° C (30).
Fluorescent immunolabeling
Fixed cells on glass slides (FisherPlus slides, Fisher Scientific Co.), chamber slides (Lab-Tek,
Inc.), or Aclar® coverslips were briefly rehydrated in Tris-buffered saline, pH 7.5, and then
blocked by incubation in Tris-buffered saline, pH 7.5 containing 1% (w/v) bovine serum albumin
(Sigma Immunologicals) for 60 min. Slides were then rinsed five times with Tris-buffered
saline, pH 7.5 and incubated for 1-3 h with primary antibodies diluted in the above blocking
buffer (typically 1:100 to 1:200 dilutions). Slides were then washed five times as before and
treated with either anti-mouse or anti-rabbit IgG Fc-domain secondary antibodies conjugated to
FITC or TRITC fluorochromes diluted 1:1000 in blocking buffer (Jackson Immunoresearch and
Molecular Probes, Inc.). After washing off unbound secondary antibody, specimens were
stained with 1 µg/ml 4',6-diamidino-2-phenylindole (DAPI), mounted with VectaShield (Vector
Labs.), and slides cover slipped prior to imaging with a Leica TCS-SP AOBS (True Confocal
Scanner-SpectroPhotometer Acousto-Optic Beam Splitter) equipped with 4 lasers (Krypton,
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Argon, UV, and HeNe), or a Nikon Microphot Fx epifluorescence microscope outfitted with a
SPOT-RT CCD digital camera (Diagnostic Instruments). Digital images were post-processed
with Adobe Photoshop (v 6.0).
Cell death assay
Apoptotic cells were detected in UMR cultures using a cell death detection kit (Boehringer
Mannheim). Cultures were fixed in 2% paraformaldehyde in phosphate buffered saline and
processed according to the manufacturer's instructions. Samples were incubated with a Terminal
deoxynucleotidyl transferase dUTP Nick End Labeling (TUNEL) reaction mixture that adds
fluorescein-conjugated dUTP to the free 3'-OH groups in single- and double-strained DNA
fragments within apoptotic nuclei. After washing, the specimens were stained with alizarin red S
(see above) and then 1 µg/ml DAPI, followed by mounting in VectaShield. All fluorochromes
were detected using confocal microscopy. TUNEL specificity was determined by omitting the
terminal deoxynucleotidyl transferase necessary for adding dUTP to the free 3'-OH ends of DNA
strands.
Electron microscopy
For conventional electron microscopy, cultures were fixed for 24 hours with 2% glutaraldehyde
in 150 mM sodium cacodylate, pH 7.2, at 4° C. Samples were post-fixed in 1% OsO4,
dehydrated, embedded, sectioned and stained according to published protocols (19,30). For
ultrastructural immunocytochemistry, tissue samples were fixed with 2% formaldehyde in PBS,
overnight at 4° C. Samples were cryo-protected, frozen in liquid nitrogen and sectioned as
described previously (37), using a method adapted from that of Tokuyasu (38). Frozen sections
80-100 nm thick were processed for indirect immunolabeling using secondary antibodies
coupled to 6 nm or 12 nm colloidal gold (Jackson Immunoresearch, West Grove, PA), under
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conditions designed to minimize cross-reactivity and non-specific binding of antibodies (37). In
some cases, sections were decalcified by floating them on a drop of ice-cold 10% trichloroacetic
acid for 60 min. prior to immunolabeling. Sections were examined using a JEOL 1200EX
transmission electron microscope at an accelerating voltage of 100 kV.
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Results
Mineralizing UMR cultures produce focal deposits of apatite that also contain BSP and
alkaline phosphatase activity
When given an organophosphate stimulant like β-GP, UMR cultures deposit an apatite mineral
phase by a utilization of phosphate ions released from β-GP by alkaline phosphatase (19,30).
Figure 1A demonstrates the focal nature of the biomineralization process in UMR cultures after
β-GP exposure, and also reveals the close spatial relationship between BSP and apatite deposits
in this biomineralization model system. Figure 1B shows that these focal areas of apatite in
UMR cultures also stain positive for alkaline phosphatase activity. BSP has been reported to
accumulate quantitatively in these focal areas prior to the detection of an apatite phase, thereby
meeting the necessary temporal-spatial requirements of a matrix protein involved in apatite
formation (30). However, it is not clear how BSP is targeted to these biomineralization foci
(BMF) prior to mineral deposition.
BMF are located within the extracellular matrix between UMR cells
Figure 1C shows X-Y and X-Z views from a three-dimensional stack of confocal images each
representing an optical slice of 0.5 µm depth. BMF are identified by their strong immuno-
staining for BSP, while nuclei are identified by their strong staining with DAPI. These 3D
images demonstrate that BMF are located in the extracellular matrix space between cells, and
that nearly all BMF are devoid of staining for the presence of double-stranded DNA. Further,
BMF neither stain positively with the TUNEL reaction nor exhibit evidence of DAPI-stained
apoptotic bodies (Fig. 1D). Taken together, the absence of DNA remnants, of TUNEL-positive
signal, and of apoptotic bodies indicates that BMF are not apoptotic or necrotic cell debris. These
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results strengthen the conclusions from our previous studies (19,30) that the biomineralization
process in UMR cultures is not dystrophic.
The 3D confocal dataset in Figure 1C shows that an average BMF is spherical in shape
with typical dimensions of 10-20 µm in X-Y and 10-15 µm in the X-Z viewing planes. Notably,
not all negatively charged macromolecules secreted into the extracellular space are deposited in
BMF as indicated by the lack of overlap between the Alizarin red/BSP signals and hyaluronan
staining (Fig. 1C). Thus, the incorporation of BSP into BMF is unlikely to result from
nonspecific electrostatic interactions. Rather, the data suggest that the strict BSP deposition in
BMF is due to more specific interactions.
Bone Acidic Glycoprotein-75 is a biomarker for BMF precursors prior to active
mineralization
Figures 2 and 3 demonstrate for the first time that spherical BMF precursors are recognizable as
BAG-75 containing supramolecular complexes prior to the addition of β-GP into UMR cultures.
Briefly, Figures 2B and 2D depict the representative brightfield appearance of UMR monolayer
cultures at 64 h of incubation, just after confluence has been reached, but prior to
organophosphate addition (“zero-time”). At this time, the cultures consist of a confluent
monolayer of UMR cells containing two size populations of refractile, roughly spherical BMF
precursors (15-25 µm and 150-250 µm in diameter), which project upward from the cell layer at
apparently random intervals. After immunostaining, BAG-75 was detected in both size
populations of BMF precursors prior to initiating mineralization (Figs. 2A and 2C). The
immunofluorescent signal for BAG-75 within the larger BMF precursors consisted of several
bright focal areas each 10-20 µm in diameter embedded within a slightly lower level of diffuse
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staining (Fig. 2C). This appearance suggests that the larger sized BMF precursors may represent
a cluster of smaller ones.
Both sizes of BMF precursors were able to nucleate calcium phosphate crystals when
UMR cultures were incubated for an additional 24 h with medium containing β-GP (i.e., 64 h to
88 h after plating). This is evident by the strong staining obtained with alizarin red-S dye
binding to large (Figs. 2E, 2F, and 5E) and small BMF (Fig. 5E). Several points can be made
regarding the relative staining patterns observed when BAG-75 immunofluorescence and alizarin
red-S-stained mineral crystals are imaged together. At low magnification, the stronger alizarin
red-S signal displays a punctate appearance comprised of numerous 10-20 µm diameter round
deposits within the interior domain of the larger BMF (Fig. 2E). In contrast, the BAG-75
immunofluorescence signal appears as a layer surrounding the alizarin red-S-stained deposits
and, internally, in junctional areas separating individual alizarin red-S-stained deposits (Fig. 2F).
In these undecalcified cultures, the regions of strongest alizarin red-S staining are seemingly
devoid of apparent BAG-75 staining, while BAG-75 staining is readily visible in the outer layer
surrounding the mineral deposits and within the internal areas physically separating alizarin red-
S-stained round deposits. This apparent lack of BAG-75 immunogenicity deeper within these
larger BMF may be due to the coverage of antigenic sites by the hydroxyapatite crystalline
phase. This point is documented upon decalcification of mineralized cultures as seen in the next
section.
Thus, in UMR cultures, BAG-75 is a biomarker both for BMF precursors prior to
initiating mineralization, and for mature BMF containing mineral crystals regardless of size.
Within the larger BAG-75-enriched mature BMF, the apatite mineral deposits seem to be
organized into small domains (10-20 µm) having sizes similar to those of the smaller BMF.
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Again, this appearance suggests that the larger sized BMF precursors may represent a cluster of
smaller ones.
BAG-75-enriched focal deposits represent the initial sites of mineralization in primary
calvarial osteoblastic cultures
The presence of BMF in the UMR osteoblastic culture system raises the possibility that
structures like these may also exist in primary osteoblastic cultures. Figures 3D and 3E indicate
that initial focal mineral deposits in fetal rat calvarial osteoblastic cell cultures have structural
features and dimensions similar to those of UMR BMF. When partially decalcified by EDTA,
these focal sites stain positively for the presence of BAG-75 (Fig. 3F and 3G). Two other
characteristics of mineralization in primary osteoblastic cultures are consistent with that
occurring in BMF in UMR cultures (Figure 2): (a) the focal area for BAG-75 immunostaining is
larger than the focal area measurement for alizarin red-S staining (compare Figs. 3D with 3F,
and Figs. 3E with 3G), and (b) focal BAG-75 staining temporally precedes that of apatite
deposition (for example, compare Figs. 3A and 3B with Figs. 3D and 3F). Additional support
for the concept that BMF are the sites of mineral nucleation in many osteoblastic model systems
is shown in Figure 3H-J. Non-transformed osteoblastic cell line MC3T3-E1 exhibits focal
alizarin red-S stained mineral deposits similar to those observed in UMR cultures (Figs. 3H and
3I) that also stain positively for the presence of BAG-75 after partial decalcification using EDTA
(Fig. 3J).
Decalcification reveals that the BAG-75 content increases within BMF during active
mineralization
Since the results above suggest that BAG-75 epitopes might be partially blocked by
hydroxyapatite mineral deposits, it was important to show that this antigenicity could be
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recovered upon decalcification. To this end, replicate UMR cultures at 64 h of incubation were
treated with or without β-GP supplementation for 24 h. Mineralized cultures were fixed and then
decalcified using EDTA chelation (Figure 4) or other decalcification methods (30). Atomic
absorption measurement of elemental calcium determined that these treatments released more
than 98% of the original calcium content of fully mineralized cultures (30). In the absence of
confounding mineral crystals, a large increase in BAG-75 signal is observed indicating that the
BAG-75 content of BMF is substantially increased over the 24 h mineralization period (Fig. 4).
This accumulation of BAG-75 occurs only after addition of β-GP to the UMR cultures, as
control cultures not exposed to β-GP over the same time frame do not exhibit this increase in
BAG-75 immunofluorescence (data not shown). Thus, as shown previously for BSP (30), the
content of BAG-75 epitope within BMF increases during active mineralization.
When decalcification solutions were recovered and processed for Western blotting with
anti-BAG-75 (data not shown) or BSP antibodies (30), very little BAG-75 or BSP protein was
detectable in these fractions. These findings indicate that most of the BAG-75 and BSP epitopes
are not solubilized by decalcification of mineralized cultures. This suggests that most of the
BAG-75 and BSP accumulated within BMF is not the result of adsorption to pre-existing
hydroxyapatite crystals. A similar conclusion was made with respect to the BAG-75 present at
sites of initial mineral nucleation in primary bone [see Gorski et al., companion paper (29)].
BSP co-localizes to large and small BMF containing BAG-75
Without β-GP, BSP is predominantly secreted into the media by UMR cells, though after β-GP is
added, BSP rapidly accumulates within supramolecular complexes that subsequently mineralize
(30). We demonstrate in Figure 5 that these extracellular sites in mineralizing UMR cultures
seem to be the same as BMF precursors enriched in BAG-75 and recognizable in zero-time
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cultures without β-GP (Figs. 2 and 4). In fully mineralized cultures, BSP was localized within
both large (Fig. 5G,H) and small (Fig. 5C,H) mature BMF, which also stained strongly for BAG-
75 (Figs. 4 and 5A). Note that the shape and boundaries of the areas of BSP staining
corresponded exactly with those delimited by BAG-75 immunostaining (Fig. 5D, overlay
image). The physical characteristics and BAG-75 content of the small BMF precursors seen in
Figs. 2 and 4A-D identify them as similar structures. Interestingly, although many BMF
exhibited a strong immunofluorescence signal for both proteins (Fig. 5D, arrows), some small
BMF structures displayed noticeably lower levels of co-staining. These findings could be due to
differences in mineral content, which may lead to blocking of antigens.
Altogether, these results demonstrate that BSP begins to accumulate in BAG-75-enriched
BMF after the addition of β-GP, but prior to nucleation of hydroxyapatite crystals (30).
Ultrastructural analysis of BMF during active mineralization of UMR cultures
The X-Z view from the confocal imaging shown in Figure 1C indicates that small BMF are
roughly spherical in shape with a diameter range of 10-20 µm. The X-Z ultrastructural image of
a BMF in a mineralizing UMR culture (Fig. 6A) indicates that these confocal estimates are quite
accurate. The inset scanning EM image in Figure 6A also shows that the overall dimension and
shape of supramolecular complexes formed by purified BAG-75 protein are similar to those of
small BMF observed in mineralized UMR cultures.
BMF are filled with both thin fibrillar and granular substances (Fig. 6B). In addition,
BMF contain what appear as translucent round structures of 300-800 nm diameter, and electron
opaque round structures of 50-200 nm in diameter (Figs 6, A-C). BMF did not, however, exhibit
evidence of opaque, rounded structures having a classic appearance of condensed chromatin or
apoptotic bodies (39,40). This finding is consistent with DAPI- and TUNEL-staining analyses
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shown in Figures 1C and 1D, respectively. A comparison of BMF during mineralization (Fig.
6C) as compared to unmineralized controls (Fig. 6D) indicates that the only visible differences
are that the former are completely filled with fibrillar, granular and vesicular structures with little
void space (Fig. 6C, inset), whereas the latter exhibit more void space and are less granular in
appearance (Fig. 6D, inset).
Figures 6B and 7C (arrowhead) show clearly that there are two distinct size classes of
spherical shaped structures within mineralized BMF. One population, ranging in diameters of 50-
200 nm, has a highly opaque core with a discernable 6-8 nm thick trilaminar-delimiting
boundary (i.e., “dark-light-dark”) consistent with the ultrastructural characteristics of a
phospholipid membrane (Fig. 7C, arrowhead). These smaller sized structures resemble the
ultrastructural appearance of matrix vesicles (1,3,5,8). Another larger sized population (Figs. 6B
asterisks, and 7C), ranging in diameters from 300-800 nm, has a relatively translucent core and a
10-20 nm thick boundary surrounding the entire structure. Within mineralizing BMF, both the
small and large spherical structures appear to come in close contact with each other at their
surfaces (Figs. 6B, inset and Fig. 7C).
Localization of BAG-75 and BSP within BMF at the ultrastructural level
Figures 2E and 2F demonstrate that the inner core of the BMF contains more apatite mineral than
its outer boundaries. Within the inner core of BMF, the immunogold particles indicating the
locations of BSP were generally distributed on 10-nm thin-filament fibrils (Fig. 7A, arrows).
Towards the outer surface of BMF, BSP immunogold particles were generally associated with
larger vesicles, but not the smaller ones (Figs. 7B and 7C, arrows versus arrowheads,
respectively). Close inspection of the gold-particle staining pattern on these larger structures
gives the impression that BSP epitopes are on the surface. This is particularly evident for the
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structure shown in Figure 7C (arrow) where gold particles were only observed in a location that
appeared to cut tangentially across the vesicle surface. Non-immune antibody control sections
typically contained a few immunogold particles, usually present in groups of one or two, but
never in clusters as large as those shown here (see Figure 3C in this paper, and Figure 7E in the
Gorski et al. companion paper for images of non-immune antibody staining).
Double staining for BAG-75 and BSP using different sized immunogold particle
antibodies (12 nm and 6 nm, respectively) revealed that these two bone matrix proteins are co-
localized in the outer boundary region of BMF (Fig. 8). BAG-75 epitopes were enriched in the
outermost layer while BSP epitopes were underneath this layer within submicron spatial
resolution of each other. What is interesting about this outer region of BMF is that it represents
the boundary between unmineralized and mineralized matrix areas (Figs. 2E and 2F). BAG-75
immunogold particles were difficult to detect within the core of BMF possibly reflecting the
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Discussion
This study has revealed that BAG-75 is expressed very early during the biomineralization
process of UMR 106-01 BSP osteoblastic cultures. Furthermore, this study provides evidence
that focal extracellular deposition sites enriched in BAG-75 accurately predict the location of
subsequent active mineral nucleation in mineralizing osteoblastic cultures. This finding may be
a general feature of all osteoblastic cultures undergoing in vitro biomineralization since UMR,
primary fetal calvarial, and MC3T3-E1 osteoblastic model systems share this property. While
sharing a common enrichment in BAG-75, mineralized BMF sites in these models display some
structural differences in overall size (smaller in MC3T3-E1 than in UMR or FRC cultures) and
shape (more 3-dimensional in UMR than in MC3T3-E1 and FRC cultures). We hypothesize that
relative differences in secretion rates of individual BMF components (vesicles, BSP, BAG-75) or
in the local distribution of cells committed to osteogenic differentiation may contribute to such
distinctions.
BAG-75 is a biomarker for locating the future positions of BMF, and we refer to these
BAG-75-enriched areas prior to mineral formation as BMF precursors. Two size populations of
these spherical supramolecular extracellular complexes were recognized morphologically and by
virtue of their enrichment in BAG-75. Shortly after the addition of β-GP, an inducer of
mineralization, UMR cultures begin to quantitatively accumulate BSP within these BAG-75-
enriched BMF precursors (30). A few hours later, these BAG-75- and BSP-enriched BMF then
deposit hydroxyapatite within, thereby converting them into mature BMF. Regardless of mineral
content, BAG-75 is consistently present within the outer layer of mineralized BMF suggesting a
role in defining the dimensions of the forming mineralized matrix. A similar expression pattern
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of BAG-75 in developing bone implies it participates in setting the boundary limits of new
mineralized trabeculae [see Gorski et al., companion paper (29)].
As the earliest recognized biomarker of BMF, we hypothesize that BAG-75 serves two
roles, one as a structural scaffold and the other as a source of phosphate ions for apatite
nucleation. With regard to its first function, we propose that BAG-75 plays a key role in the
initial assembly of the structural scaffold of BMF precursors. This is supported by evidence that
purified BAG-75 protein alone is able to self-assemble into thin linear strands of up to 1 micron
in length (24,27,41). These BAG-75 microfibrils can coalesce to form supramolecular spherical
structures of up to 10-15 microns in diameter (Fig. 5A, inset), which have the capability to retain
large quantities of phosphate ions (24). These structures are remarkably similar in shape and
dimension to the smaller BAG-75-enriched BMF identified here in UMR cultures.
We further rationalize that such a BAG-75 framework could provide key secondary
binding sites to recruit other proteins, such as BSP or alkaline phosphatase, required for
subsequent nucleation of hydroxyapatite. Despite excellent morphological descriptions of
membranous bone formation during embryogenesis (42), few matrix protein biomarkers have
been identified which uniquely define future sites of osteogenesis. Zhu et al. (43) found that
BSP message was weakly expressed in the center of mesenchymal cartilaginous condensations at
14 days of gestation in the mouse. In the current study, we demonstrate that BAG-75
accumulation in the extracellular matrix precedes the deposition of even BSP, and represents one
of the earliest matrix protein markers for sites of biomineralization.
Alkaline phosphatase also appears to be expressed very early during osteogenesis (44-
46), and an elevated expression of alkaline phosphatase has been used to define committed
proliferating osteogenic cells (14). As described in our BMF model of mineralization below,
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alkaline phosphatase is an important component of matrix vesicles (47,48), where it is believed
to produce inorganic phosphate ions from complex phosphate sources to feed the process of
crystal nucleation. Addition of alkaline phosphatase inhibitors such as levamisole blocks UMR
biomineralization reactions initiated by β-GP (19). With regard to its second functional role in
UMR biomineralization, we hypothesize that the de-phosphorylation of BAG-75 protein itself
could also provide a potential source of phosphate ions for apatite nucleation reactions since this
protein contains an estimated 44-phosphoryl residues/mole (22).
Debate continues regarding the underlying mechanism(s) of vertebrate biomineralization.
One view proposes that phospholipid membrane-delimited vesicles (matrix vesicles) released
into the extracellular matrix by osteoblasts mediate biomineralization reactions (1,3,5,8,49).
They are reported to exist in nearly all mineralizing tissues, but are best described in calcifying
cartilage. They are small (50-200 nm diameter) vesicles containing high levels of
phosphatidylserine and cardiolipin (50,51). They contain several enzymes including alkaline
phosphatase and pyrophosphatase (52), and have cytoskeletal (53) and matrix proteins (54)
associated with their inner and outer membrane surfaces, respectively. Another
biomineralization theory proposes that noncollagenous protein structures assembled within the
type I collagen-rich, extracellular matrix of osteoid directly mediates the heterogeneous
nucleation of apatite crystals (2,7,55). Based on the presence of polyacidic domains and a
capacity to nucleate hydroxyapatite in vitro, BSP has been proposed to act as such a nucleator in
bone and cartilage (21).
Yet another biomineralization theory proposes that calcified spherically shaped structures
with a size range of 300-600 nm in diameter, termed crystal ghost aggregates, nucleate the initial
apatite crystals within osteoid and then subsequently seed a heterogeneous nucleation reaction
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within the fibrillar collagen matrix (3,4,56,57-59). These mineralized structures in bone tissue
stain positive with acridine orange or ruthenium red suggesting the presence of sulfate groups
(4,60). This staining was originally interpreted as evidence for sulfated proteoglycans in these
structures (61). However, it is possible that a sulfated glycoprotein could also contribute to these
sulfate groups. BSP has been shown to co-localize with crystal ghost aggregates in osteoid (18)
and in osteoblastic cultures (20,30); it also contains several sulfate groups bound to
oligosaccharides and tyrosine residues (62,63). Interestingly, BSP has not yet been reported to
be a component of matrix vesicles (1,47,49,64). Our findings indicate that BSP is associated
with a population of large vesicle-like structures, but not with the smaller matrix vesicles. In this
way, BSP may define a biochemically distinct population of vesicles, which are larger than
matrix vesicles. Since apatite mineral forms in association with these “bioapatite vesicles” (65),
we hypothesize that these larger vesicles may be related to, and likely an early structural stage of,
the fully mineralized BSP-enriched particles referred to as crystal ghost aggregates (3,4).
It is suggested that the large size, amorphous character, and prior lack of an authentic
biomarker for BMF precursor and mature BMF complexes may have prevented their routine
detection with ultrastructural methods, which tends to emphasize discrete electron-opaque
structures of uniform appearance (e.g., matrix vesicles). Despite this limitation, similar
spherical, interfibrillar regions containing crystal ghost aggregates enriched in BSP and an
amorphous extracellular matrix have been identified in vitro (66,67) and in vivo (68) as sites of
subsequent initial mineral nucleation. In addition, Irie et al. (67) have noted the apparent
similarity between these nucleation sites in vitro and those present in membranous or primary
bone. The above-mentioned studies suggest that BMF-like structures have been observed before,
but seem to have been considered obscure entities lacking a clear context with respect to
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mineralization reactions. It is our contention that only with data such as that provided by our
current study can one properly interpret the significance of these structures to the
biomineralization process.
We propose a 5-step biomineralization model (Fig. 9) in which BMF, typically 15-25 µm
in diameter, serve as a supramolecular domain that facilitates the initial sequestration of calcium
and phosphate ions in an extracellular matrix environment. Step 1 involves the determination of
the boundaries, shape, and size of future mineralized matrix areas by BAG-75 expressing cells.
Step 2 involves the assembly of extracellular BMF precursor structures via BAG-75 self-
assembly reactions. Step 3 involves the accumulation of matrix vesicles and bioapatite vesicles
within the BMF precursor matrix. We envision that the large amount of membrane surface area
within BMF packed with vesicles could facilitate heterogeneous nucleation reactions through
adsorption and concentration of required proteins and ions. Upon the introduction of an
organophosphate stimulant, Step 4 involves the recruitment of required accessory proteins such
as BSP, and the continued accumulation of BAG-75 into the BMF. We suggest that BMF-bound
BSP would function to sequester calcium ions in proximity to copious amounts of phosphate ions
associated with BAG-75. Together these events could lead to the supersaturation conditions
necessary to nucleate hydroxyapatite crystals on the vesicle surfaces within BMF. Finally, Step
5 involves the growth of these seed crystals and the formation of mineralized aggregates.
Continued self-assembly of BAG-75 at the outer boundaries could foster new matrix growth
within individual BMF. Future studies will investigate potential protein-protein interactions of
monomeric and oligomeric BAG-75 complexes with BSP. In addition, identification, isolation
and characterization of the structure and function of BMF precursors are now feasible by
following their BAG-75 biomarker.
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Acknowledgements
RJM wishes to acknowledge the support of grants from the NIH (AR-45171) and The Lerner
Research Institute of The Cleveland Clinic Foundation. JPG wishes to acknowledge the support
of grants from the NIH (DE-14619 and DE-11197) and University of Missouri Research Board.
The authors acknowledge the expert assistance with confocal imaging by Dr. Judith Drazba
(Imaging Facility at The Lerner Research Institute), and with electron microscopy by Jessica
Kueker (Univ. of Missouri-Kansas City). We thank Dr. Mark McKee, McGill University, and
Dr. Sarah Dallas, Univ. of Missouri School of Dentistry for providing the MC3T3-E1 and fetal
rat calvarial cell cultures, respectively, and Dr. Bjorn R. Olsen, Harvard University for his
careful critique of the manuscript prior to submission.
Footnotes
1 Abbreviations: β-GP, beta-glycerophosphate; BMF, biomineralization foci; BSP, bone
sialoprotein; BAG-75, bone acidic glycoproteins-75; FITC, fluorescein isothiocyanate; TRITC,
Texas red isothiocyanate; TUNEL, Terminal deoxynucleotidyl transferase dUTP Nick End
Labeling; DAPI, 4',6-diamidino-2-phenylindole; EM, electron microscopy; bioapatite vesicles,
300-600 nm diameter translucent vesicular structures within BMF; matrix vesicles, 50-200 nm
diameter opaque vesicular structures exhibiting a trilaminar membrane and accumulating within
BMF, and FRC, fetal rat calvarial.
2 Presented in preliminary form at the 25th Annual Meeting of the American Society for Bone
and Mineral Research, Minneapolis, MN, September 2003.
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Figure Legends
Figure 1. Mineralizing UMR cultures deposit BSP and calcium mineral in extracellular
matrix complexes referred to as BMF. Panel A shows a UMR culture that had been treated
with β-GP for 24 h, and immunostained with anti-BSP monoclonal WV1D1(9C5) followed by
alizarin red S staining. BSP is denoted by the green color, while calcium mineral is denoted by
the red color (AR-S). DIC, differential interference contrast view of the same field of view.
Color overlay panel shows both the green and red color bands represented in a full RGB color
spectrum. Panel B shows a UMR culture that had been treated with β-GP for 24 h, and
immunostained with anti-BSP monoclonal WV1D1(9C5) followed by Vector Red alkaline
phosphatase activity staining. BSP is denoted by the green color, while alkaline phosphatase
activity is denoted by the red color. The white arrowheads point to BMFs that stain positive for
both BSP and alkaline phosphatase activity. Panel C depicts a 3D confocal analysis of a
mineralizing UMR culture. BSP is denoted by the green color, hyaluronan is denoted by the red
color, and DAPI-stained nuclei are indicated by the blue color. The X-Y view is a single 0.5-µm
slice at the indicated depth in the X-Z view panel. Panel D shows the results of a FITC-TUNEL
assay on a 24 h mineralized UMR culture. Top panel shows a color overlay of the TUNEL
(green) and alizarin red-S-stained calcium mineral (red) fluorescence. Bottom panel shows a
color overlay of the TUNEL (green), calcium mineral (red), and DAPI-stained nuclei (blue).
Note that calcium mineral deposits do not co-localize with either DAPI-stained or TUNEL-
stained nuclei, and that only about 1-2% of the nuclei are TUNEL-positive in this field of view.
Figure 2. BAG-75 is a biomarker for precursors of BMF prior to nucleation of mineral
crystals. Panels A-D are representative of confluent UMR cultures at 0 h prior to the addition of
β-GP; E and F are representative of cultures 24 h after the addition of β-GP. A and B, C and D,
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and, E and F, respectively, represent images of the same field of view. Panel A, Anti-BAG-75
antibodies specifically label small 15-25 micron diameter populations of BMF precursors (white
arrows). Panel B, Brightfield view of small BMF precursors (black arrows). Panel C, Anti-
BAG-75 antibodies immunostain a large 150-250 micron diameter BMF precursor (white
arrow). Panel D, Brightfield image of large 150-250 micron diameter BMF precursor (black
arrow). Panels E and F, Large mineralized BMF stained with Alizarin Red S dye (white
arrows) still stains positive for BAG-75 on its surface and within its structure (white
arrowheads). Scale bars : 200 microns for A-D and 100 microns for E and F.
Figure 3. BAG-75-enriched focal deposits represent the initial sites of mineralization in
osteoblastic cultures from primary fetal rat calvarial (FRC) cells and MC3T3-E1 cells.
Refer to the Materials and Methods section for culture details. Panel A, phase contrast view of
FRC culture after 7 days of β-GP treatment; no alizarin red-S staining was detected at this time.
Panel B, BAG-75 immunostaining of FRC culture after 7 days of β-GP treatment; same field of
view as shown in panel A. Panel C, non-immune IgG control staining of FRC culture after 7
days of β-GP treatment. Panels D and E, alizarin red-S staining of apatite deposits in FRC
culture after 17 days of β-GP treatment. Panels F and G, BAG-75 immunostained FRC culture
after 17 days of β-GP treatment after decalcification using EDTA; same fields of view as shown
in panels D and E, respectively. Panel H, brightfield view of alizarin red-S stained MC3T3-E1
(subclone M4) culture after 12 days of β-GP treatment. Panel I, higher magnification brightfield
view of an individual alizarin red-S stained foci from panel H after partial decalcification. Panel
J, BAG-75 immunostaining of MC3T3-E1 culture (subclone M4) after 12 days of β-GP
treatment; same field of view as shown in panel I. Scale bars in panels A-H are 100 microns,
while those shown in panels I and J are 2 microns.
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Figure 4. BAG-75 content of BMF increases during mineralization. Fully mineralized
cultures (24 h β-GP) were decalcified overnight with Tris-buffered saline (pH 8.0) containing 50
mM EDTA. Cultures were then processed for immunofluorescence microscopy with anti-BAG-
75 and then with Alexa-green conjugated anti-rabbit IgG antibody. For comparison, a parallel
fully mineralized culture without decalcification in shown in Figure 2E,F. Left panels, Paired
anti-BAG-75 and brightfield images of 24 h (β-GP minus) culture. Right panels, Paired anti-
BAG-75 and brightfield images of 24 h (β-GP plus) culture after decalcification. Scale bar: 20
microns.
Figure 5. BSP co-localizes to large and small BMF complexes containing BAG-75.
Confluent UMR cultures were incubated for 24 h in the presence of β-GP, fixed in ethanol, and
then processed for immunofluorescence microscopy with anti-BSP monoclonal WV1D1(9C5)
(red) and anti-BAG-75 (green) antibodies as described in Materials and Methods. Panels A-D
represent images of the same field of view containing small BMF. White and black arrows mark
BMF that stain strongly for both BAG-75 and BSP antigens. Panel D, Color overlay image for
both BSP (red) and BAG-75 (green). Panel E, Brightfield view of an Alizarin Red-S stained
culture showing the presence of many small BMF (black arrowheads) and two large BMF (black
arrows). Panels F-H are images from the same field of view containing a large and several small
BMF. Upper (Panel G) and lower (Panel H) confocal optical planes of anti-BSP stained large
BMF. Approximate displacement of images in G and H is about 15 microns (4 µm versus 19 µm
from the basal aspect of the culture, respectively). Note the presence of BSP-stained small BMF
(white arrows) and intracellular BSP staining of individual cells within the surrounding
monolayer (white arrowheads) in this lower optical plane only. Scale bars: panel D, 50
microns; panels E-G, 200 microns.
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Figure 6. Ultrastructural views of BMF. Panel A shows a view cut perpendicular to the
culture surface through a single BMF from a mineralizing UMR culture incubated for 12 h in the
presence of β-GP, then fixed and processed for electron microscopy as described in Materials
and Methods. The black line shown roughly 2 µm above the basal aspect of the culture
represents the relative position of a 100 nm thin-section along a plane parallel to the culture
surface representing the viewing planes shown in panels B-D. Inset shows a scanning EM view
of two supramolecular complexes formed spontaneously from purified BAG-75 (24). Panel B
shows a view of small and large spherical structures within a mineralizing BMF. The
arrowheads indicate the locations of 50-200 nm diameter opaque structures having an
ultrastructural appearance similar to matrix vesicles. The asterisks indicate the locations of 300-
600 nm diameter translucent spheres that we refer to as bioapatite vesicles. The inset in the right
panel is a higher magnification view of the small and large vesicles indicated by the arrowhead
and asterisk at the top of the right panel. Note how both vesicular structures appear to touch each
other’s surfaces. Panels C and D show views cut parallel to the culture surface through a
mineralizing BMF (panel C), and a BMF precursor from a non-mineralizing control (panel D);
note the healthy looking cells near the BMF areas. Boxes in panels C (left) and D (left) are areas
shown at higher magnification in their respective right panels. Arrows in panel C (left) indicate
positions of other BMF not shown at higher magnification in panel C (right). Insets are higher
magnification views of the boxed areas in panels C (right) and D (right).
Figure 7. Ultrastructural view of a mineralizing BMF stained with anti-BSP antibody LF-
87. Panel A, the arrows indicate the positions of matrix areas containing clusters of more than
ten 12-nm gold particles. The immunogold particles appear associated with thin filament fibrils
and not banded fibrillar collagen structures. Panel B, the arrows indicate the positions of clusters
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of immunogold particles associated with the larger translucent bioapatite vesicles. Arrowheads
indicate the positions of structures that resemble matrix vesicles, and do not contain associated
gold particles. Panel C, a higher magnification view of both large and small vesicular structures.
Arrow indicates a region of the larger structure containing a cluster of immunogold particles that
appears to be at its surface. Arrowhead indicates a clear view of the trilaminar-delimiting
boundary surrounding the smaller vesicle. Note how both larger and smaller vesicles appear to
touch each other’s surfaces.
Figure 8. Ultrastructural view of a mineralizing BMF stained with both anti-BAG-75 and
anti-BSP WV1D1 (9C5) antibodies. Panel A, the box indicates an area of the BMF near its
outer boundary shown at higher magnification in panel B. Panel B, the area labeled “BAG-75”
indicates the position of a large cluster of 12-nm immunogold particles identifying BAG-75
epitopes associated with thin filament fibrils. The box labeled “BSP” indicates the position of a
cluster of 6-nm immunogold particles identifying BSP epitopes. Inset shows a higher
magnification view of the 6-nm gold particles. Note that submicron distances separate both 12-
nm and 6-nm gold particles.
Figure 9. Diagram depicting the UMR biomineralization model. Times shown in steps 4 and
5 refer to organophosphate exposure times. Note that BSP is not retained within the BMF
precursor containing BAG-75 (steps 2 and 3) until an organophosphate stimulant is added to the
culture (step 4), at which time BSP is then retained in the BMF matrix.
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FIGURES
Figure 1
DC
A B
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Figure 3 (new)
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Figure 6A
Figure 6B
X-Z view
BMF
A
B
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Figure 6C and 6D
C
D
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GorskiRonald J. Midura, Aimin Wang, Dinah Lovitch, Douglas Law, Kimerly Powell and Jeff P.
sialoprotein accumulation and apatite nucleation in osteoblastic culturesBone acidic glycoprotein-75 delineates the extracellular sites of future bone
published online March 5, 2004J. Biol. Chem.
10.1074/jbc.M312409200Access the most updated version of this article at doi:
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