This core will provide each of the projects with high quality tissue section, histochemistry, immunochemistry, and in situ hybridization for the in vivo analysis of pancreatic islet functions under various conditions of transplantation or genetic manipulation. The core will provide paraffin, cryostat blocks, and tissue sections for each of the projects, perform histochemical assays and Hematoxylin and Eosin counter staining, as well as carry out immunofluorescence and horseradish peroxidase-based immunodetection on paraffin embedded and cryo-preserved tissue sections. The reproducibility and standardization of these techniques are extremely important to compare transplanted or transgenic animals to controlled littermates. A similar histology core has just been set up for the Gene Therapy Program here at he University of Chicago under the directorship of Dr. Jeffrey Leiden, with whom several of the investigators work closely. It is anticipated that the increased need for tissue fixation, embedding, sectioning, and staining will make an expansion of the currently existing core facilities available. The core will also provide each of the projects with purified islets for their studies as needed. The core will be directed by Dr. Yijun Zeng, who has extensive experience in isolation and manipulation of pancreata as well as islet cell purification. In addition, the core will be staffed by a senior histology technician with experience in light microscopy, immunohistochemistry, and in situ hybridization. A dedicated technician is needed because of the expected large number of tissue samples that will be examined in each of the projects within the program.

Project Start
1998-06-01
Project End
1999-05-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
4
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Szot, Gregory L; Yadav, Mahesh; Lang, Jiena et al. (2015) Tolerance induction and reversal of diabetes in mice transplanted with human embryonic stem cell-derived pancreatic endoderm. Cell Stem Cell 16:148-57
Bluestone, Jeffrey A; Buckner, Jane H; Fitch, Mark et al. (2015) Type 1 diabetes immunotherapy using polyclonal regulatory T cells. Sci Transl Med 7:315ra189
Bour-Jordan, Hélène; Bluestone, Jeffrey A (2009) Regulating the regulators: costimulatory signals control the homeostasis and function of regulatory T cells. Immunol Rev 229:41-66
Bluestone, Jeffrey A; Kuchroo, Vijay (2009) Autoimmunity. Curr Opin Immunol 21:579-81
Meagher, Craig; Tang, Qizhi; Fife, Brian T et al. (2008) Spontaneous development of a pancreatic exocrine disease in CD28-deficient NOD mice. J Immunol 180:7793-803
Kabak, Shara; Clark, Marcus R (2004) Membrane-targeted peptides derived from Igalpha attenuate B-cell antigen receptor function. Biochem Biophys Res Commun 324:1249-55
McFarland, B J; Katz, J F; Beeson, C et al. (2001) Energetic asymmetry among hydrogen bonds in MHC class II*peptide complexes. Proc Natl Acad Sci U S A 98:9231-6
Salomon, B; Rhee, L; Bour-Jordan, H et al. (2001) Development of spontaneous autoimmune peripheral polyneuropathy in B7-2-deficient NOD mice. J Exp Med 194:677-84
Chatenoud, L; Salomon, B; Bluestone, J A (2001) Suppressor T cells--they're back and critical for regulation of autoimmunity! Immunol Rev 182:149-63
O'Herrin, S M; Slansky, J E; Tang, Q et al. (2001) Antigen-specific blockade of T cells in vivo using dimeric MHC peptide. J Immunol 167:2555-60

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