Worldwide, diarrhea claims several million lives annually, mostly those of infants. Poverty, crowding, and contaminated water supplies all contribute. Although its incidence is much lower in the more affluent nations, diarrhea remains one of the two most common visits to pediatric emergency rooms and is also common among the institutionalized elderly. Diarrhea is also a troublesome gastrointestinal complication of diabetes. Major salt and water absorption in the intestine is mediated by electroneutral NaCl absorption, consisting of a Na+/H+ exchanger coupled with a Cl-/HCO3- exchanger. The Na+/H+ exchanger isoform 3 (NHE3) is often targeted in many diarrheal diseases. However, the molecular basis and biological factors regulating NHE3 are not fully understood. This is an important aspect as a better understanding of the mechanisms activating NHE3 should aid the development of improved therapeutic modalities to combat diarrhea caused by the inhibition of Na+/H+ exchange. During the previous funding cycle, we have demonstrated that lysophosphatidic acid (LPA) activates NHE3 via LPA5R in colon epithelial cells and showed that LPA is a potent activator of NHE3 and fluid absorption in mouse intestine. In addition, we showed that the effect of LPA involves apical epidermal growth factor receptor (EGFR). However, the mechanism of LPA-induced EGFR transactivation and the activation of NHE3 are incompletely studied.
We aim to determine the molecular mechanism of NHE3 regulation by LPA and test the importance of LPA5R in vivo (Specific Aim 1). Diabetic diarrhea is a troublesome gastrointestinal complication of type 1 diabetes. Our preliminary data show that mice with diabetes induced by streptozotocin (STZ) develop diarrhea and NHE3 activity is significantly attenuated. Our study further shows that insulin stimulates NHE3 activity in STZ-treated mice, although the underlying mechanisms are unknown. We will determine the molecular mechanism of NHE3 activation by insulin and test the utility of LPA as an activator of NHE3 and fluid absorption in the type 1 diabetic model in rodent (Specific Aim 2). Our preliminary data show that metformin commonly used for glycemic control in type 2 diabetes inhibits NHE3 activity, further suggesting a causal role of NHE3 in diabetes-related diarrhea. Our data show that NHE3 is ubiquitinated in response inhibitory agents, such as metformin, phorbol ester, and forskolin. Surprisingly, we observed a significant difference in ubiquitination of NHE3 between human and non-human. The status of NHE3 ubiquitination and its role have never been investigated.
In Specific Aim 3, we will investigate the mechanisms that regulate NHE3 ubiquitination and the importance of ubiquitination in NHE3 regulation and EPEC-induced diarrhea. Successful completion of the proposed work will increase the knowledge of molecular mechanism of NHE3 regulation and will provide insights into improved strategies for treatment and prevention of diarrheal diseases.

Public Health Relevance

Diarrhea is a common cause of death in developing countries and the second most common cause of infant deaths worldwide. Secretory diarrhea occurs when there is increased secretion, decreased absorption, or both so that there is a net loss of electrolytes and fluid. Na+/H+ exchanger type 3 (NHE3) present in the apical membrane of the small intestinal and colonic epithelia plays a major role in Na+ and fluid absorption. NHE3 is often targeted in many diarrheal diseases and the mechanisms of the inhibition of NHE3 have widely been studied. However, it is important to realize that a better understanding of biological factors and mechanisms activating NHE3 should aid the development of improved therapeutic modalities to counteract diarrheal diseases. The main objective of this application is to continue our investigation to understand the molecular mechanisms of NHE3 activation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK061418-11
Application #
8492071
Study Section
Special Emphasis Panel (ZRG1-DKUS-C (03))
Program Officer
Grey, Michael J
Project Start
2002-06-01
Project End
2016-08-31
Budget Start
2013-09-01
Budget End
2014-08-31
Support Year
11
Fiscal Year
2013
Total Cost
$327,425
Indirect Cost
$117,537
Name
Emory University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
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Lin, Songbai; Yeruva, Sunil; He, Peijian et al. (2010) Lysophosphatidic acid stimulates the intestinal brush border Na(+)/H(+) exchanger 3 and fluid absorption via LPA(5) and NHERF2. Gastroenterology 138:649-58
Schmieg, John; Yang, Guangli; Franck, Richard W et al. (2010) A multifactorial mechanism in the superior antimalarial activity of alpha-C-GalCer. J Biomed Biotechnol 2010:283612

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