The goals of this training program in autoimmunity and connective tissue biology are unchanged. We plan to recruit talented and highly motivated graduate students and postdoctoral fellows and provide these individuals with a first class training program that will prepare them for competitive and independent careers in academic research. The research interests of the program encompass faculty in 6 departments within the medical school (Biochemistry, Medicine, Microbiology, Pathology, Pharmacology/Toxicology, and Physiology) and span a wide range of interest fundamental to basic understanding of autoimmunity and the cellular nad molecular biology of connective tissue disease: cellular immunology, regulation of gene expression, organelle trafficking, membrane signal transduction and secretion, rheumatic disease model, and the structure-function relationship of cytokines and their receptors. Thus, a considerable breadth of experimental and conceptual choices exist for potential trainees, including animal models of disease that should enhance our ability to attract and train M.D.'s interested in careers in academic medicine. The strength of the Training Program continues to be its outstanding faculty, consisting of 17 well-funded faculty with vigorous on-going research programs, utilizing an array of state-of-the-art molecular and cellular techniques. The training programs continues to benefit from the excellent facilities and the recent growth of the already strong graduate programs that lead to the Ph.D. degree in either Molecular and Cellular Biology, Physiology, and Pharmacology/Toxicology. These programs currently house 110 graduate students, with (at this early date (4/98) an entering class of 38 students already committed from a pool of over 400 applicants. Corresponding growth in the MD/PhD program has occurred, who are represented along with medical students and MDs doing research in these laboratories. The training program in autoimmunity and connective tissue biology is interdisciplinary and highly interactive, with exposure to diverse areas of faculty expertise in the basic and clinical sciences in a number of formats which include formal course work, intimate seminars, individual tutorials and several weekly seminar series and journal clubs. These forums facilitate the high level of faculty-student interaction that is traditional at Dartmouth and results in the recognition of our research efforts at both the national and international level.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32AR007576-07
Application #
6171472
Study Section
Arthritis and Musculoskeletal and Skin Diseases Special Grants Review Committee (AMS)
Program Officer
Ader, Deborah N
Project Start
1994-07-01
Project End
2004-04-30
Budget Start
2000-05-01
Budget End
2001-04-30
Support Year
7
Fiscal Year
2000
Total Cost
$180,028
Indirect Cost
Name
Dartmouth College
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
03755
Zhang, Tong; Sentman, Charles L (2013) Mouse tumor vasculature expresses NKG2D ligands and can be targeted by chimeric NKG2D-modified T cells. J Immunol 190:2455-63
Jensen, Amy L; Collins, Jane; Shipman, Emilie P et al. (2012) A subset of human uterine endometrial macrophages is alternatively activated. Am J Reprod Immunol 68:374-86
Schmucker, Adam C; Wright, Jason B; Cole, Michael D et al. (2012) Distal interleukin-1? (IL-1?) response element of human matrix metalloproteinase-13 (MMP-13) binds activator protein 1 (AP-1) transcription factors and regulates gene expression. J Biol Chem 287:1189-97
Zhang, Tong; Wu, Ming-Ru; Sentman, Charles L (2012) An NKp30-based chimeric antigen receptor promotes T cell effector functions and antitumor efficacy in vivo. J Immunol 189:2290-9
Rigby, William F C; Wu, Yee Ling; Zan, Moe et al. (2012) Increased frequency of complement C4B deficiency in rheumatoid arthritis. Arthritis Rheum 64:1338-44
Pendergrass, Sarah A; Lemaire, Raphael; Francis, Ian P et al. (2012) Intrinsic gene expression subsets of diffuse cutaneous systemic sclerosis are stable in serial skin biopsies. J Invest Dermatol 132:1363-73
Hodge, Christine A; Tran, Elizabeth J; Noble, Kristen N et al. (2011) The Dbp5 cycle at the nuclear pore complex during mRNA export I: dbp5 mutants with defects in RNA binding and ATP hydrolysis define key steps for Nup159 and Gle1. Genes Dev 25:1052-64
Zhang, Tong; Sentman, Charles L (2011) Cancer immunotherapy using a bispecific NK receptor fusion protein that engages both T cells and tumor cells. Cancer Res 71:2066-76
Rutkowski, Melanie R; Stevens, Cynthia A; Green, William R (2011) Impaired memory CD8 T cell responses against an immunodominant retroviral cryptic epitope. Virology 412:256-68
Cai, Xiongwei; Gaudet, Justin J; Mangan, James K et al. (2011) Runx1 loss minimally impacts long-term hematopoietic stem cells. PLoS One 6:e28430

Showing the most recent 10 out of 55 publications