This is a Competing Renewal application for continued support of an NHLBI (Lung Division) Post-Doctoral Training Grant, which is currently in its 20th year in the Medical School, Department of Pathology at the University of Michigan.
The aim of this program is to provide in depth training in basic research to holders of MD, PhD or DVM degrees. The research areas of focus include lung inflammation (mediators and regulators), complement, apoptosis, DNA repair, immunopathology (including the roles of oxidants, proteases, cytokines, chemokines) and endothelial cell biology. Since inception, the program has been led by Professor Peter A. Ward. Currently all trainees are assigned to research laboratories in the Department of Pathology. Trainees flow smoothly between laboratories because of the close collaborative interactions between preceptors. The program features weekly research seminars and six annual and formal seminars on ethics in research. This training program has an impressive record of training MD's and PhD's, the majority of whom hold academic appointments. Over the past five years a concerted effort has been successful in recruiting trainees from under-represented racial/ethnic groups. The intellectual and scientific environment at the University of Michigan Medical center is very enriched for the trainees. The many core scientific facilities in the Medical School greatly enhance opportunities for trainees involved both in bench laboratory research and in animal research. The setting of the program in the context of a large academic medical center provides special advantages to trainees who can take advantage of the relevance of fundamental biomedical research to clinical diseases. This long established training program with a proven record of success positions the program to be very competitive and successful in recruitment of candidates for appointment as post-doctoral fellows.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Institutional National Research Service Award (T32)
Project #
5T32HL007517-24
Application #
6740888
Study Section
Special Emphasis Panel (ZHL1-CSR-M (F1))
Program Officer
Colombini-Hatch, Sandra
Project Start
1986-07-01
Project End
2006-05-31
Budget Start
2004-06-01
Budget End
2005-05-31
Support Year
24
Fiscal Year
2004
Total Cost
$121,889
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Pathology
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Bringman-Rodenbarger, Lauren R; Guo, Angela H; Lyssiotis, Costas A et al. (2018) Emerging Roles for SIRT5 in Metabolism and Cancer. Antioxid Redox Signal 28:677-690
Habiel, David M; Espindola, Milena S; Coelho, Ana L et al. (2018) Modeling Idiopathic Pulmonary Fibrosis in Humanized Severe Combined Immunodeficient Mice. Am J Pathol 188:891-903
Fattahi, Fatemeh; Frydrych, Lynn M; Bian, Guowu et al. (2018) Role of complement C5a and histones in septic cardiomyopathy. Mol Immunol 102:32-41
Werner, Jessica L; Escolero, Sylvia G; Hewlett, Jeff T et al. (2017) Induction of Pulmonary Granuloma Formation by Propionibacterium acnes Is Regulated by MyD88 and Nox2. Am J Respir Cell Mol Biol 56:121-130
Zeng, M Y; Inohara, N; Nuñez, G (2017) Mechanisms of inflammation-driven bacterial dysbiosis in the gut. Mucosal Immunol 10:18-26
Pickard, Joseph M; Zeng, Melody Y; Caruso, Roberta et al. (2017) Gut microbiota: Role in pathogen colonization, immune responses, and inflammatory disease. Immunol Rev 279:70-89
Kalbitz, Miriam; Fattahi, Fatemeh; Herron, Todd J et al. (2016) Complement Destabilizes Cardiomyocyte Function In Vivo after Polymicrobial Sepsis and In Vitro. J Immunol 197:2353-61
He, Yuan; Hara, Hideki; Núñez, Gabriel (2016) Mechanism and Regulation of NLRP3 Inflammasome Activation. Trends Biochem Sci 41:1012-1021
Xu, Jing; Li, Li; Xiong, Jie et al. (2016) MLL1 and MLL1 fusion proteins have distinct functions in regulating leukemic transcription program. Cell Discov 2:16008
Zeng, Melody Y; Cisalpino, Daniel; Varadarajan, Saranyaraajan et al. (2016) Gut Microbiota-Induced Immunoglobulin G Controls Systemic Infection by Symbiotic Bacteria and Pathogens. Immunity 44:647-658

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