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Mouse ghrelin-O-acyltransferase (GOAT) plays a critical role in bile acid reabsorption.

Authors :
Kang K
Schmahl J
Lee JM
Garcia K
Patil K
Chen A
Keene M
Murphy A
Sleeman MW
Source :
FASEB journal : official publication of the Federation of American Societies for Experimental Biology [FASEB J] 2012 Jan; Vol. 26 (1), pp. 259-71. Date of Electronic Publication: 2011 Sep 29.
Publication Year :
2012

Abstract

Ghrelin is a unique peptide gut hormone that requires post-translational modification to stimulate both feeding and growth hormone release. Ghrelin O-acyltransferase (GOAT) was identified as a specific acyl-transferase for ghrelin, and recent genetic deletion studies of the Goat gene (Goat(-/-)) uncovered the role of ghrelin in the regulation of glucose homeostasis. To further understand the physiological functions of the GOAT/ghrelin system, we have conducted a metabolomic and microarray profile of Goat-null mice, as well as determined Goat expression in different tissues using the lacZ reporter gene. Serum metabolite profile analysis revealed that Goat(-/-) mice exhibited increased secondary bile acids >2.5-fold. This was attributed to increased mRNA and protein expression of the ileal sodium-dependent bile acid transporter (ISBT) in the intestinal and biliary tract. Increased expression of additional solute carrier proteins, including Slc5a12 (>10-fold) were also detected in the small intestine and bile duct. Goat staining was consistently observed in the pituitary glands, stomach, and intestines, and to a lesser extent in the gallbladder and pancreatic duct. This is the first report that the GOAT/ghrelin system regulates bile acid metabolism, and these findings suggest a novel function of GOAT in the regulation of intestinal bile acid reabsorption..

Details

Language :
English
ISSN :
1530-6860
Volume :
26
Issue :
1
Database :
MEDLINE
Journal :
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Publication Type :
Academic Journal
Accession number :
21965605
Full Text :
https://doi.org/10.1096/fj.11-191460