immunology and pathology core
DESCRIPTION
Immunology and Pathology Core. Core Directors Joan W. Berman, PhD and Sunhee C Lee, MD Departments of Pathology and Microbiology and Immunology Staff Members Lillie Lopez and Namjong Choi. Core Aims. - PowerPoint PPT PresentationTRANSCRIPT
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Immunology and Pathology Core
Core DirectorsJoan W. Berman, PhD and Sunhee C Lee, MD
Departments of Pathology and Microbiology and Immunology
Staff MembersLillie Lopez and Namjong Choi
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Core AimsAim 1. To provide investigators with the research infrastructure and
optimization of technologies and protocols to perform state-of-the art immunologic and biochemical assays. These assays will quantify responses of cells infected with or stimulated by HIV and AIDS-associated pathogens.
Aim 2. To provide cell isolation and tissue culture service Aim 3. To provide investigators with a facility using appropriate biohazard
containment that is capable of examining the effects of infection with HIV and AIDS-associated pathogens on tissues by characterizing morphological, molecular and phenotypical changes using histological, immunohistochemical, in situ hybridization analyses and live cell imaging.
Aim 4. To train CFAR investigators in the performance of techniques that are extant in the Core and to assist investigators in the development of new immunological assays and pathological techniques. To provide extensive mentoring in the immunology and pathogenesis of HIV/AIDS and OI.
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Core Training programs
• Provide training in microscopy, RNA and protein techniques
• Provide training in immunopathology• Provide training in data analysis and presentation• Provide mentoring for project development relevant
to the immunopathology of HIV/AIDS and OI • Provide grant writing assistance for protocols and
experimental approaches
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Core services• Histopathology
– customize fixation and tissue processing and sectioning, frozen and fixed• Immunohistochemistry
– optimize primary and secondary antibodies and provide control tissues• Cytokine and Chemokine and other soluble mediator measurements (ELISA, multiplex assays, FACS, MSD)
– Optimize and customize assay protocols• RNA analysis (Q-RT-PCR)
– Identify and test primers and optimize assay conditions• Protein extraction and analysis
– Interface with proteomic core (imaging MS)• Culture of human and rodent CNS cells (endothelial cells, astrocytes, microglia and neurons)• Isolation of PBMCs and subsets (monocytes, T cells, B cells and progenitors)• Live cell imaging
– available for HIV-infected tissue and cells– calcium imaging– time-lapse photography
• Fluorescence and confocal microscopy– Customize and optimize appropriate reagents– Provide control tissues and reagents
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Expansion & Innovation ofCore Activities
• Addition of new microscope and live cell imaging• Addition of human PBMC and subset isolation service
and training• Imaging mass spectroscopy with Proteomics Facility• Addition of assistance with grant writing:
experimental design and methods
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Microglial reactivity in human cerebral malaria
Sarah Hochman, MD, “Malaria/HIV co-infection”
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Recent Improvements to Live Cell imaging Facility
• Now have Cy2, Cy3, Cy5 and Cy7 filters• A new objective for low magnification • Incubation system with CO2, O2 and humidity control and heating stages• Longer times for live cell imaging• Anti-vibration table with compressor• New software for calcium imaging and time lapse microscopy
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Microscope setupUpgrade, including incubation system, CO2,
and O2 control plus software
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Use of Live cell imaging system
Eliseo Eugenin et al., submitted
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Imaging mass spectrometry (iMS)
Nature Reviews 2010
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•Greater sensitivity and a linear dynamic range (at least 5 logs)•Ability to perform instantaneous detection of binding with minimal or no need for washing steps (advantage for low affinity interactions and kinetically sensitive measurements)•Can perform up to 10 analyses per well
MSD Electrochemiluminescence
Figure. Multiplex cytokine analysis with the MSD system. Capture mAbs are printed on the MSD plate well surface in defined positional arrays. Up to 10 spots can be printed by the manufacturer per well. The MSD Sector Imager plate scanner detects and quantitates light emitted from each spot separately, allowing multiple analytes to be quantitated using a mixture of detection mAbs. (Figure adapted from MSD website, http://www.meso-scale.com).
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Conclusion
Immunology and Pathology Core provides state-of-the art services, consultation, and
mentoring to facilitate outstanding HIV/OI research programs