The purpose of the Morphology Core has been and will continue to be to perform tissue processing and staining, immunohistochemistry, and in situ hybridization for Program investigators and their associates. Because each project in this renewal proposes numerous experiments requiring histological processing of samples and microscopic detection techniques, the Morphological Core will be an integral and essential component of this Program Project Grant. The Morphology Core will be staffed by experienced research technicians and will occupy dedicated and fully equipped laboratory space. To expedite the processing of samples, the Core will be organized into functional subcompartments, or laboratories, that are defined by the services provided. The Histology Laboratory will process samples, cut sections, perform histological staining, and store tissue blocks. The Immunology laboratory will perform immunostaining, assist investigators in preparing immunoreagents, and maintain commonly used materials. The Molecular Biology Laboratory will be responsible for in situ hybridization procedures, including labeling probes and storing reagents. Tissues and cell samples will be collected and submitted by personnel associated with the individual investigators. Project investigators or their associates will complete a Work Order form that will be used to catalogue the work requested and to record the date that each task is completed. The quality and results of analytical assays will be reviewed by Drs. Parks and Crouch with the Project leaders or the co- investigator who is responsible for the experiment. Furthermore, the Morphology Core will, as it has done for the past two funding cycle, provide a center for correlative interactions among the Program investigators in their independent, yet complementary studies on lung biology.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL029594-17
Application #
6202224
Study Section
Project Start
1999-09-01
Project End
2000-08-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
17
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Barnes-Jewish Hospital
Department
Type
DUNS #
City
Saint Louis
State
MO
Country
United States
Zip Code
63110
Byers, Derek E; Wu, Kangyun; Dang-Vu, Geoffrey et al. (2018) Triggering Receptor Expressed on Myeloid Cells-2 Expression Tracks With M2-Like Macrophage Activity and Disease Severity in COPD. Chest 153:77-86
Wu, Kangyun; Byers, Derek E; Jin, Xiaohua et al. (2015) TREM-2 promotes macrophage survival and lung disease after respiratory viral infection. J Exp Med 212:681-97
Gharib, Sina A; Edelman, Jeffery D; Ge, Lingyin et al. (2015) Acute cellular rejection elicits distinct microRNA signatures in airway epithelium of lung transplant patients. Transplant Direct 1:
Pan, Jie-Hong; Adair-Kirk, Tracy L; Patel, Anand C et al. (2014) Myb permits multilineage airway epithelial cell differentiation. Stem Cells 32:3245-56
Rohani, Maryam G; Pilcher, Brian K; Chen, Peter et al. (2014) Cdc42 inhibits ERK-mediated collagenase-1 (MMP-1) expression in collagen-activated human keratinocytes. J Invest Dermatol 134:1230-1237
Holtzman, Michael J; Byers, Derek E; Alexander-Brett, Jennifer et al. (2014) The role of airway epithelial cells and innate immune cells in chronic respiratory disease. Nat Rev Immunol 14:686-98
Holtzman, Michael J; Byers, Derek E; Brett, Jennifer-Alexander et al. (2014) Linking acute infection to chronic lung disease. The role of IL-33-expressing epithelial progenitor cells. Ann Am Thorac Soc 11 Suppl 5:S287-91
Gu, Xiaoling; Karp, Philip H; Brody, Steven L et al. (2014) Chemosensory functions for pulmonary neuroendocrine cells. Am J Respir Cell Mol Biol 50:637-46
Byers, Derek E; Alexander-Brett, Jennifer; Patel, Anand C et al. (2013) Long-term IL-33-producing epithelial progenitor cells in chronic obstructive lung disease. J Clin Invest 123:3967-82
Chen, Peter; Edelman, Jeffrey D; Gharib, Sina A (2013) Comparative evaluation of miRNA expression between in vitro and in vivo airway epithelium demonstrates widespread differences. Am J Pathol 183:1405-1410

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