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Impaired mucin synthesis and bicarbonate secretion in the colon of NHE8 knockout mice
Author(s) -
Hua Xu,
Bo Zhang,
Jing Li,
Chunhui Wang,
Huacong Chen,
Fayez K. Ghishan
Publication year - 2012
Publication title -
ajp gastrointestinal and liver physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.644
H-Index - 169
eISSN - 1522-1547
pISSN - 0193-1857
DOI - 10.1152/ajpgi.00146.2012
Subject(s) - knockout mouse , conditional gene knockout , villin , biology , endocrinology , medicine , apical membrane , small intestine , secretion , mucin 2 , large intestine , mucin , sodium–hydrogen antiporter , microbiology and biotechnology , sodium , epithelium , chemistry , gene expression , biochemistry , receptor , phenotype , gene , actin , genetics , organic chemistry
Sodium/hydrogen exchanger 8 (NHE8), the newest member of the SLC9 family, is expressed at the apical membrane of the epithelial cells in the intestine and the kidney. Although NHE8 has been shown to be an important player for intestinal sodium absorption early in development, its physiological role in the intestine remains unclear. Here, we successfully created a NHE8 knockout (NHE8(-/-)) mouse model to study the function of this transporter in the intestinal tract. Embryonic stem cells containing interrupted NHE8 gene were injected into mouse blastocyst to produce NHE8(+/-) chimeras. NHE8(-/-) mice showed no lethality during embryonic and fetal development. These mice had normal serum sodium levels and no signs of diarrhea. Apically expressed NHE2 and NHE3 were increased in the small intestine of the NHE8(-/-) mice in compensation. The number of goblet cells and mucin (MUC)-positive cells in the colon was reduced in NHE8(-/-) mice along with mucosal pH, MUC2 expression as well as downregulated in adenoma (DRA) expression. Therefore, the role of NHE8 in the intestine involves both sodium absorption and bicarbonate secretion.

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