The principal investigator's interest has been in the developmental aspects of electrolyte transport across the intestinal epithelium. Initially, the PI.. utilized in vivo perfusion and in vitro plasma membrane vesicles to define the transport processes of Na+ and Cl transport across the enterocytes. The developmental pattern of these processes, and their regulation was defined. The current proposal will extend knowledge acquired during the tenure of the grant to explore and identify the intestinal Na+/H+ exchangers at the brush border and basolateral membranes of the enterocyte of the rat and their regulation during development. The brush border Na+/H+ exchanger functions as part of the neutral Na+/Cl transport process; whereas, the basolateral exchanger functions as a regulator of intracellular Ph and cell volume. We have shown developmental changes in the transport characteristics of both exchangers in regard to their kinetics and amiloride sensitivity. Moreover, the amiloride sensitivity of both exchangers is markedly deferent indicating encoding by two separate genes.
The specific aims of the proposal are; 1) Clone and sequence the full length rat cDNA encoding the brush border and basolateral Na+/H+ exchanger using probes derived from human Na+/Ha+ exchanger cDNA.2) determine chromosomal assignment of both exchangers and whether they are encoded by two separate genes. 3. Determine the chromosomal localization of the Na+/H= exchanger loci by genetic linkage analysis and identify genetic markers (Restriction fragment length polymorphism [RFLPs] and Polymerase Chain Reaction amplification product RFLP's for use in studies of infants with defect in the brush border Na+/H+ exchanger. 40 Express the brush border and basolateral Na+/H+ exchanger in xenopus Laevis oocytes and in exchanger deficient cells. 50 Determine the tissue distribution of Na=/H+ exchangers expression during maturation (suckling, weanling, and adolescent rats) and expression along villus-crypt axis by Northern blotting and in situ hybridization using cDNA'S of both exchangers as probes. 6) Further localize the site of Na+/H= exchange expression by Western blotting and immunocytochemistry using polyclonal antibodies against both exchangers. 7) Determine if both exchangers are phosphoproteins and whether second messengers affect their phosphorylation. 8) Determine the structure- function relationship of both exchangers.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK041274-07
Application #
2141680
Study Section
General Medicine A Subcommittee 2 (GMA)
Project Start
1988-09-01
Project End
1995-06-30
Budget Start
1994-09-01
Budget End
1995-06-30
Support Year
7
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Pediatrics
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Harrison, Christy A; Laubitz, Daniel; Ohland, Christina L et al. (2018) Microbial dysbiosis associated with impaired intestinal Na+/H+ exchange accelerates and exacerbates colitis in ex-germ free mice. Mucosal Immunol 11:1329-1341
Gurney, Michael A; Laubitz, Daniel; Ghishan, Fayez K et al. (2017) Pathophysiology of Intestinal Na+/H+ exchange. Cell Mol Gastroenterol Hepatol 3:27-40
Ghishan, Fayez K; Kiela, Pawel R (2017) Vitamins and Minerals in Inflammatory Bowel Disease. Gastroenterol Clin North Am 46:797-808
Laubitz, Daniel; Harrison, Christy A; Midura-Kiela, Monica T et al. (2016) Reduced Epithelial Na+/H+ Exchange Drives Gut Microbial Dysbiosis and Promotes Inflammatory Response in T Cell-Mediated Murine Colitis. PLoS One 11:e0152044
Kiela, Pawel R; Ghishan, Fayez K (2016) Physiology of Intestinal Absorption and Secretion. Best Pract Res Clin Gastroenterol 30:145-59
Wang, Aiping; Ling, Zongxin; Yang, Zhixiang et al. (2015) Gut microbial dysbiosis may predict diarrhea and fatigue in patients undergoing pelvic cancer radiotherapy: a pilot study. PLoS One 10:e0126312
Larmonier, C B; Shehab, K W; Ghishan, F K et al. (2015) T Lymphocyte Dynamics in Inflammatory Bowel Diseases: Role of the Microbiome. Biomed Res Int 2015:504638
Johansson, Malin E V; Gustafsson, Jenny K; Holmén-Larsson, Jessica et al. (2014) Bacteria penetrate the normally impenetrable inner colon mucus layer in both murine colitis models and patients with ulcerative colitis. Gut 63:281-91
Ghishan, Fayez K; Kiela, Pawel R (2014) Epithelial transport in inflammatory bowel diseases. Inflamm Bowel Dis 20:1099-109
Larmonier, Claire B; Laubitz, Daniel; Hill, Faihza M et al. (2013) Reduced colonic microbial diversity is associated with colitis in NHE3-deficient mice. Am J Physiol Gastrointest Liver Physiol 305:G667-77

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