Gastroenterology
Volume 138, Issue 2 , Pages 649-658, February 2010

Lysophosphatidic Acid Stimulates the Intestinal Brush Border Na+/H+ Exchanger 3 and Fluid Absorption via LPA5 and NHERF2

  • Songbai Lin

      Affiliations

    • Division of Digestive Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia
  • ,
  • Sunil Yeruva

      Affiliations

    • Department of Gastroenterology, Hepatology, and Endocrinology, Hannover Medical School, Hannover, Germany
  • ,
  • Peijian He

      Affiliations

    • Division of Digestive Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia
  • ,
  • Anurag Kumar Singh

      Affiliations

    • Department of Gastroenterology, Hepatology, and Endocrinology, Hannover Medical School, Hannover, Germany
  • ,
  • Huanchun Zhang

      Affiliations

    • Division of Digestive Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia
  • ,
  • Mingmin Chen

      Affiliations

    • Department of Gastroenterology, Hepatology, and Endocrinology, Hannover Medical School, Hannover, Germany
  • ,
  • Georg Lamprecht

      Affiliations

    • Department of Medicine, University of Tübingen, Tübingen, Germany
  • ,
  • Hugo R. de Jonge

      Affiliations

    • Department of Biochemistry, Erasmus University Medical Center, Rotterdam, The Netherlands
  • ,
  • Ming Tse

      Affiliations

    • Departments of Medicine and Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland
  • ,
  • Mark Donowitz

      Affiliations

    • Departments of Medicine and Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland
  • ,
  • Boris M. Hogema

      Affiliations

    • Department of Biochemistry, Erasmus University Medical Center, Rotterdam, The Netherlands
  • ,
  • Jerold Chun

      Affiliations

    • Department of Molecular Biology, Scripps Research Institute, La Jolla, California
  • ,
  • Ursula Seidler

      Affiliations

    • Department of Gastroenterology, Hepatology, and Endocrinology, Hannover Medical School, Hannover, Germany
  • ,
  • C. Chris Yun

      Affiliations

    • Division of Digestive Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia
    • Department of Physiology, Emory University School of Medicine, Atlanta, Georgia
    • Corresponding Author InformationReprint requests Address requests for reprints to: C. Chris Yun, PhD, Division of Digestive Diseases, Emory University School of Medicine, Whitehead Building, Room 201, 615 Michael Street, Atlanta, Georgia 30322

Received 9 July 2009; accepted 23 September 2009. published online 05 October 2009.

Background & Aims

Diarrhea results from reduced net fluid and salt absorption caused by an imbalance in intestinal absorption and secretion. The bulk of sodium and water absorption in the intestine is mediated by Na+/H+ exchanger 3 (NHE3), located in the luminal membrane of enterocytes. We investigated the effect of lysophosphatidic acid (LPA) on Na+/H+ exchanger activity and Na+-dependent fluid absorption in the intestine.

Methods

We analyzed the effects of LPA on fluid absorption in intestines of wild-type mice and mice deficient in Na+/H+ exchanger regulatory factor 2 (NHERF2; Nherf2−/−) or LPA2 (Lpa2−/−). Roles of LPA5 and NHERF2 were determined by analysis of heterologous expression.

Results

Under basal conditions, LPA increased fluid absorption in an NHE3-dependent manner and restored the net fluid loss in a mouse model of acute diarrhea. Expression of the LPA receptor LPA5 was necessary for LPA-induced stimulation of NHE3 activity in colonic epithelial cells. Stimulation of NHE3 by the LPA-LPA5 signaling required coexpression of NHERF2, which interacted with LPA5. LPA-mediated intestinal fluid absorption was impaired in Nherf2−/− mice, demonstrating the requirement for NHERF2 in LPA5 activity. However, fluid absorption was unaltered in Lpa2−/− mice. LPA stimulated NHE3 and fluid absorption in part by increasing NHE3 protein abundance at the brush border membrane of intestinal epithelial cells.

Conclusions

LPA is a potent stimulant of NHE3 and fluid absorption in the intestine, signaling through LPA5. Regulation by LPA5 depends on its interaction with NHERF2. LPA might be useful in the treatment of certain diarrheal diseases.

Abbreviations used in this paper: Apc, adenomatous polypopsis coli, BSA, bovine serum albumin, CT, cholera toxin, CFTR, cystic fibrosis transmembrane conductance regulator, LPA, lysophosphatidic acid, mRNA, messenger RNA, NHE3, Na+/H+ exchanger type 3, NHERF, Na+/H+ exchanger regulatory factor, OK, opossum kidney, PBS, phosphate-buffered saline, PCR, polymerase chain reaction, PDZ, postsynaptic density 95, discs large, and zonula occludens–1, PDZK1, PDZ domain containing protein in kidney 1, RT, reverse transcription, TNF-α, tumor necrosis factor−α, WT, wild-type

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 30.00 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 Conflicts of interest The authors disclose no conflicts.

 Funding This work was funded by National Institutes of Health grants DK061416 (CCY), MH51699 and HD50685 (JC) and by DFG SFB621-C9 (US). SL was supported by the Crohn's and Colitis Foundation of America. PH was supported by the American Heart Association. AS and MC were supported by postdoctoral stipends of the Hannover biomedical Research School that were funded by the DAAD and Abbot GmbH via the “matching fund” program. We thank the Emory Digestive Disease Research Development Center (supported by DK064399) for the use of light microscope and the Zeiss 510 confocal microscope and the Volkswagen Stiftung for funding of the Leica LSM.

PII: S0016-5085(09)01750-8

doi:10.1053/j.gastro.2009.09.055

Gastroenterology
Volume 138, Issue 2 , Pages 649-658, February 2010