phenotypic and functional characterization of ... · hematopoiesis lymphopoiesis bone marrow spleen...
TRANSCRIPT
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Hematopoiesis
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Hemato – Lymphopoiesis
Hematopoiesis Lymphopoiesis
Bone Marrow
Spleen
Thymus
Lymph nodes
Spleen
Bone marrow
Cells (erythrocytes,
granulocytes, monocytes,
platelets) circulate in blood
and tissues
Cells (lymphocytes}
circulate in
lymph/tissues
Some of them in
blood
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Properties of Hematopoietic
Stem Cell (HSCs)
• Self-renewal
• Quiescence
• High resistance to radio-chemotherapy and
cytostatic drugs
• Characteristic morphology (e.g., large nucleus,
euchromatin)
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Hematopoietic Stem Cells
• A hematopoietic stem cell (HSC) possesses the ability for self-renewal and may differentiate into any blood cell from both the myeloid and lymphoid lineages.
• During embryogenesis HSC migrate from one to another anatomical site. This developmental journey of the HSC starts with the primitive streak/yolk sac (YS) and aorta gonado mesonephros (AGM) region and continues through the fetal liver (FL) to their final destination in the bone marrow (BM).
• HSC, during the differentiation process, give rise to more mature hematopoietic progenitor cells (HPC) that lose the ability for self renewal; however, they are able to grow colonies containing functional hematopoietic cells.
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Origin of HSC
• HSC are among the first stem cells that are specified during
embryogenesis from epiblast (primitive ectoderm).
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Origin of HSC
• Definitive primitive pre-HSC expand in the YS, and when the
developing heart tube begins to propel the first hematopoietic cells
in vessels (> E8.25), primitive pre-HSC become detectable in the
embryo proper and colonize the luminal surface of the aorta in the
so-called aorta-gonado-mesonephros region (AGM) or para-aortic
splanchnopleure (P-Sp).
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Stem cells are travellers
• The colonization of BM by HSC does not terminate the developmental journey of HSC. After symmetric division one of a daughter HSC has to leave the BM niche and is released into the circulation in order to find a new niche.
• This mechanism may be responsible for maintaining homeostasis between HSC niches in different areas of BM that is distributed across various bones.
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Tissues
Organs
BloodBone
Marrow
Lymph
Bone
Marrow
Trafficking - Immunosurveillance by circulating
Stem Cells
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SDF-1
gradient
CXCR4
SDF-1
gradient
SDF-1
gradient
SDF-1
gradient
SDF-1
gradient
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Phosphatases
SHIP 1
SHIP 2
CD45
MEK
MAPK p42/44
PI-3K
AKT
Adhesion
Fak
Paxillin
p130 CAS
Jak, Tyk
Elk-1 STAT
Biological effects
CXCR4
SDF-1
I B NF- B
NF- B
CXCR4 - SDF-1 Axis
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Retention in BM
Homing to BM
CXCR4+ HSCs
Developmental
Migration
SDF-1
CXCR4
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Stem Cell Niches
• Stem cell niche describes the microenvironment in which stem cells reside and which interacts with stem cells to regulate stem cell fate (quiescence vs. self renewal and differentiation).
• Several factors have been identified that regulate stem cell characteristics within the niche including adhesion molecules, extracellular matrix components, the oxygen tension, growth factors, cytokines, and physiochemical nature of the environment including the pH, ionic strength and metabolites.
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Bone Marrow
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Stem Cell Niches
• Stem cell niche describes the microenvironment in which stem cells reside and which interacts with stem cells to regulate stem cell fate (quiescence vs. self renewal and differentiation).
• Several factors have been identified that regulate stem cell characteristics within the niche including adhesion molecules, extracellular matrix components, the oxygen tension, growth factors, cytokines, and physiochemical nature of the environment including the pH, ionic strength and metabolites.
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Bone Marrow stem cell niches
Hormones
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HSC DIVISIONS
SYMETRIC ASYMETRIC
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Bone Marrow Examination
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Hematopoietic Growth Factors
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Kit LigandKL
c-kit receptor
- Growth factors for many type of cells
- KL or c-kit receptor deficiency – anemia,
- Activates early steps of hematopoiesis
- Activates mast cells
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Erytropoietin
- Secreted by kidneys
- Regulated by hypoxia
- Required for red cell development
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Trombopoietin
- Scented by liver, kidney and spleen
- Secretion regulated by blood platelet number
- Stimulates megakaryopoiesis and
thrombopoiesis
- 20% of blood platelets may be produced in TpO
defcient mice
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G-CSFGranulocyte colony stimulating factor
- Stimulates myelopopoiesis (granulocyto-monopoiesis)
- Employed to mobilize HSCs from bone marrow into
peripheral blood
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Progenitor Cell Assays
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Clonogeneic Assays
Cytokines +
Growth Factors
Colonies
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HSC
Kit ligand (KL), Interleukin-1, Interleukin-3,
Angiopoietin-1, Trombopoietin
Kit ligand (KL)
Interleukin-3 (IL-3)
GM-CSF
CFU-Mix
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Colony Forming Unit of Mixed Lineages (CFU-GEEM)
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HSC
Kit ligand (KL), Interleukin-1, Interleukin-3,
Angiopoietin-1, Trombopoietin
Erytropoiesis
Kit ligand (KL)
Erytropoietin
Kit ligand (KL)
Interleukin-3 (IL-3)
GM-CSF
CFU-Mix
BFU-E
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Burst Forming Unit of Erythroblasts (BFU-E)
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HSC
Kit ligand (KL), Interleukin-1, Interleukin-3,
Angiopoietin-1, Trombopoietin
Erytropoiesis
Kit ligand (KL)
Erytropoietin
Megakariopoiesis
Kit Ligand (KL)
Trombopoietin
Kit ligand (KL)
Interleukin-3 (IL-3)
GM-CSF
CFU-Mix
BFU-E
CFU-Meg
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Colony Forming Unit of Megakaryocytes (CFU-Meg)
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HSC
Kit ligand (KL), Interleukin-1, Interleukin-3,
Angiopoietin-1, Trombopoietin
Erytropoiesis
Kit ligand (KL)
Erytropoietin
Megakariopoiesis
Kit Ligand (KL)
Trombopoietin
Mielopoiesis
Kit ligand (KL)
Interleukin-3 (IL-3)
GM-CSF
CFU-Mix
BFU-E
CFU-Meg
CFU-GM
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Colony Forming Unit of Granulocyte-Macrophages (CFU-GM)
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HSC
Kit ligand (KL), Interleukin-1, Interleukin-3,
Angiopoietin-1, Trombopoietin
Erytropoiesis
Kit ligand (KL)
Erytropoietin
Megakariopoiesis
Kit Ligand (KL)
Trombopoietin
Mielopoiesis
Kit ligand (KL)
Interleukin-3 (IL-3)
GM-CSF
G-CSF – granulocytes CFU-G
M-CSF – monocytes CFU-M
IL-5 – eozynophils CFU-Eos
IL-4 bazophils CFU-Baso
CFU-Mix
BFU-E
CFU-Meg
CFU-GM
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HSC
Kit ligand (KL), Interleukin-1 (IL-1),
Interleukin-3 (IL-3), Angiopoetin-1,
trombopoetin
T lymphocytes
NK Cells
B lymphocytes
IL-7
IL-7
IL-15
IL-7
IL-2
IL-7
IL-4
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Stem Cell Markers
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HSCs Receptors
CD133 CXCR4
CD34 C-KIT
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HSCs Metabolic Markers
Hoe33342
Pyronin Y
Rhodamine
123
Stem Cells are
Hoe 33341 low
Pyronin Y low
Rh 123 dim
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Hematopoietic Stem Cell
Phenotype
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Phenotype of HSCs
- CD34+ CD133+ CXCR4+ c-kit + Lin- CD45+
- Hoechst33342low, Rhodamin123low and Pyronin Ylow
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HSCs Isolation Strategies
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Magnetic separation of HSPCMACS beadsy
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FACS sorter
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Hematopoietic Transplants
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Bone Marrow Transplant
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Mobilized Peripheral Blood Transplant
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Umbilical Cord Blood Transplant
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SDF-1
SDF-1
CXCR4
HSC
CXCR4
HSC
Bone Marrow Niches
Homing - Mobilization
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Classical Pathway Alternative Pathway
C1q
C2
C4
Factor D
Factor B
C3
C5
C5b-9
Membrane Attack Complex (MAC)
Both conditioning for transplant and administration of mobilizing drugs
activates complement cascade
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Stem cell homing
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Classical Pathway Alternative Pathway
C1q
C2
C4
Factor D
Factor B
C3
C5
C5b-9
Membrane Attack Complex (MAC)
Both conditioning for transplant and administration of mobilizing drugs
activates complement cascade
Promote homing
C3a, desArgC3a
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Developmental
MigrationRetention in BM
Homing to BM
SDF-1
CXCR4
CXCR4+ HSC CXCR4+ HSC
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Janowska-Wieczorek et al. Blood 2001, 98:3143-3149
Reca et al. Blood 2003;101:3784-3793
Wysoczynski et al. Blood 2005;105:40-48
Priming
CXCR4
Responsiveness
SDF-1Bone Marrow
Mononuclear Cells
(-) (+)
Chemotaxis
to SDF-1
Priming Factor
C3a
LL37
Priming of SDF-1-CXCR4 axis by antimicrobial peptides
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Priming effect:
Increase in responsiveness to SDF-1 gradient
HSPC
SDF-1 (low dose) SDF-1 (low dose)
+
priming agent
(e.g., C3a, LL-37)
priming agent
(e.g., C3a, LL-37)
SDF-1
SDF-1
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Priming effect of C3a and LL-37 on low
doses of SDF-1
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Wysoczynski et al. Blood 2005,105, 40-48.
0
100
200
300
400
500
600
CB CFU-GM BM CFU-GM
% o
f g
raft
im
pro
vm
en
t
not primed
primed
*
*
(-)
C3a
Human BM- and UCB-derived CD34+ cells primed with
C3a engraft faster in immunodeficient mice
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Stem cell mobilization
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Stem Cell Mobilization
• Development/Organogenesis
• Physiology – circadian rhythm
• Strenous exercise
• Inflammation
• Tissue/organ injury-induced mobilization (e.g., heart
infarct, stroke)
• Pharmacological mobilization (e.g., G-CSF, AMD3100) –
HSPC circulating in PB increase up to 100 times.
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Newton’s ApplesHSCs
Blood
Retention of HSCs in the BM-niches is an active process
that counteracts continuous chemottractive gradient of
factors present in plasma (“Gravitation field analogy”).
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Ratajczak et al. Blood 2004;93:2071-2078
Wysoczynski et al. Blood 2005;105:40-48
Classical Pathway Alternative Pathway
C1q
C2 C4
Factor D
Factor B
C3
C5
C5b-9
Membrane Attack Complex (MAC)
Promote mobilization
C5a, desArgC5a
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Retention of HSCs in the BM-niches is an active process
that counteracts continuous chemottractive gradient of
factors present in plasma (“Gravitation field analogy”).
SDF-1 – CXCR4
VCAM-1 – VLA-4 ( 4 1)
AMD3100 - CXCR4 antagonist
BIO4860 - VLA-4 antagonist
MOBILIZATION
VCAM-1SDF-1
CXCR4 VLA-4
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C5-/- Mice
Normal Mice
C5 activation is required for mobilization of HSCs
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“Ice Breaker Mechanism”
“Granulocyte”
“HSC”
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Classical Pathway Alternative Pathway
C1q
C2 C4
Factor D
Factor B
C3
C5
C5b-9
Membrane Attack Complex (MAC)
Promote mobilization
C5a, desArgC5a
lytic MAC
sublytic MAC
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The lytic membrane attack complex C5b-9
(MAC) forms transmembrane channels. These
channels disrupt the phospholipid bilayer of
target cells, leading to cell lysis and death.
The sublytic (soluble) membrane attack complex C5b-9
(MAC) may bind to cell membranes, independent of any
receptor, does not lyse cells, activates multiple signaling
pathways and has wide-range effects on many cell types
leading to cellular responses, such as secretion, adherence,
aggregation, chemotaxis and even cell division.
Lytic and sub-lytic C5b-9 (MAC) in cell biology
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Sphingosine 1 phosphate
S1P
25 x higher concentration !
Bone Marrow Peripheral Blood
S1P Erythrocytes
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Activation of
myeloid cells induces
proteolytic
microenvironment
BM sinusoids
BM niche
Endothelium
HSPC
Complement
Cascade
MAC
(C5b-C9)
proteases
Gradient
S1PRBC
S1P
Mobilization
activates CC
Mobilization
activates CC
C5a
C5a
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Mobilized Peripheral Blood Transplant