This application is for a new institutional NRSA to support the training of initially two and subsequently five M.D. and Ph.D. Postdoctoral Fellows. Although a new program several of the training faculty have been highly interactive in training such individuals in the past and faculty as a whole has been highly successful in training individuals over the last ten years who now hold academic or research appointments. For example trainees who have left the program of training within the last five years show significant continuing involvement in research (approximately 70% have greater than 50% effort devoted to research). The broad objective of this program is to provide multi-disciplinary training in problem oriented research on the pathophysiology of mucosal disease with special reference to polarized epithelial and alimentary tract disorders. The training faculty consists of twenty investigators with independent, funded research programs related to this area of study. The faculty provides expertise in modern molecular, immunologic and cell biologic approaches for studying pathophysiology of disease. There exists particular emphasis on epithelial biology and immunology as it relates to epithelial biology and immunology as it relates to epithelial biology at sites such as the alimentary tract. The structure of the training program is designed to promote interactions among participating faculty and to provide trainees access to all of the laboratories and their considerable resources. Trainees are selected from graduate and clinical programs nationwide with an emphasis on identifying under-represented minorities. The major component of the training program is independent research carried out by trainees in their laboratories of choice. The training experience is further enhanced by attendance at research conferences, journal clubs and formal seminars as well as attendance in coursework largely provided by the faculty of this training program (i.e. the faculty of the training program are highly interactive in the graduate education program at Emory University School of Medicine).

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Institutional National Research Service Award (T32)
Project #
5T32DK007771-02
Application #
6176330
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Podskalny, Judith M,
Project Start
1999-07-01
Project End
2004-06-30
Budget Start
2000-07-01
Budget End
2001-06-30
Support Year
2
Fiscal Year
2000
Total Cost
$178,524
Indirect Cost
Name
Emory University
Department
Pathology
Type
Schools of Medicine
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
No, Yi Ran; He, Peijian; Yoo, Byong Kwon et al. (2015) Regulation of NHE3 by lysophosphatidic acid is mediated by phosphorylation of NHE3 by RSK2. Am J Physiol Cell Physiol 309:C14-21
Jiang, Kun; Rankin, Carl R; Nava, Porfirio et al. (2014) Galectin-3 regulates desmoglein-2 and intestinal epithelial intercellular adhesion. J Biol Chem 289:10510-7
No, Yi Ran; He, Peijian; Yoo, Byong Kwon et al. (2014) Unique regulation of human Na+/H+ exchanger 3 (NHE3) by Nedd4-2 ligase that differs from non-primate NHE3s. J Biol Chem 289:18360-72
Matthews, Jason D; Weight, Caroline M; Parkos, Charles A (2014) Leukocyte-epithelial interactions and mucosal homeostasis. Toxicol Pathol 42:91-8
Bao, Hui-Fang; Thai, Tiffany L; Yue, Qiang et al. (2014) ENaC activity is increased in isolated, split-open cortical collecting ducts from protein kinase C? knockout mice. Am J Physiol Renal Physiol 306:F309-20
Weber, D A; Sumagin, R; McCall, I C et al. (2014) Neutrophil-derived JAML inhibits repair of intestinal epithelial injury during acute inflammation. Mucosal Immunol 7:1221-32
Kamekura, R; Kolegraff, K N; Nava, P et al. (2014) Loss of the desmosomal cadherin desmoglein-2 suppresses colon cancer cell proliferation through EGFR signaling. Oncogene 33:4531-6
Liu, Bing-Chen; Song, Xiang; Lu, Xiao-Yu et al. (2013) Lovastatin attenuates effects of cyclosporine A on tight junctions and apoptosis in cultured cortical collecting duct principal cells. Am J Physiol Renal Physiol 305:F304-13
Yu, Ling; Cai, Hui; Yue, Qian et al. (2013) WNK4 inhibition of ENaC is independent of Nedd4-2-mediated ENaC ubiquitination. Am J Physiol Renal Physiol 305:F31-41
Jones, Rheinallt M; Luo, Liping; Ardita, Courtney S et al. (2013) Symbiotic lactobacilli stimulate gut epithelial proliferation via Nox-mediated generation of reactive oxygen species. EMBO J 32:3017-28

Showing the most recent 10 out of 24 publications