Document Detail


Deletion of Tis7 protects mice from high-fat diet-induced weight gain and blunts the intestinal adaptive response postresection.
MedLine Citation:
PMID:  20861213     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
After loss of intestinal surface area, the remaining bowel undergoes a morphometric and functional adaptive response. Enterocytic expression of the transcriptional coregulator tetradecanoyl phorbol acetate induced sequence 7 (Tis7) is markedly increased in a murine model of intestinal adaptation. Mice overexpressing Tis7 in intestine have greater triglyceride absorption and weight gain when fed a high-fat diet (42% energy) than their wild-type (WT) littermates fed the same diet. These and other data suggest that Tis7 has a unique role in nutrient absorptive and metabolic adaptation. Herein, male Tis7(-/-) and WT mice were fed a high-fat diet (42% energy) for 8 wk. Weight was monitored and metabolic analyses and hepatic and intestinal lipid concentrations were compared after 8 wk. Intestinal lipid absorption and metabolism studies and intestinal resection surgeries were performed in separate groups of Tis7(-/-) and WT mice. At 8 wk, weight gain was less and jejunal mucosal and hepatic triglyceride and cholesterol concentrations were lower in Tis7(-/-) mice than in the WT controls. Following corn oil gavage, serum cholesterol, triglyceride, and FFA concentrations were lower in the Tis7(-/-) mice than in the WT mice. Incorporation of oral (3)[H] triolein into intestinal mucosal cholesterol ester and FFA was less in Tis7(-/-) compared with WT mice. Following resection, crypt cell proliferation rates and villus heights were lower in Tis7(-/-) than in WT mice, indicating a blunted adaptive response. Our results suggest a novel physiologic function for Tis7 in the gut as a global regulator of lipid absorption and metabolism and epithelial cell proliferation.
Authors:
Cong Yu; Shujun Jiang; Jianyun Lu; Carrie C Coughlin; Yuan Wang; Elzbieta A Swietlicki; Lihua Wang; Ilja Vietor; Lukas A Huber; Domagoj Cikes; Trey Coleman; Yan Xie; Clay F Semenkovich; Nicholas O Davidson; Marc S Levin; Deborah C Rubin
Related Documents :
3527833 - Enzymatic and transport studies in cholesterol-fed guinea pigs using intestinal brush b...
20434963 - Dyslipidaemia-hepatic and intestinal cross-talk.
12079883 - Effects of selected anthropometric parameters on plasma lipoproteins, fatty acid compos...
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2010-09-22
Journal Detail:
Title:  The Journal of nutrition     Volume:  140     ISSN:  1541-6100     ISO Abbreviation:  J. Nutr.     Publication Date:  2010 Nov 
Date Detail:
Created Date:  2010-10-21     Completed Date:  2010-11-09     Revised Date:  2013-05-27    
Medline Journal Info:
Nlm Unique ID:  0404243     Medline TA:  J Nutr     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1907-14     Citation Subset:  IM    
Affiliation:
Division of Gastroenterology, Washington University School of Medicine, St Louis, MO 63110, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adaptation, Physiological / genetics*
Animals
Cell Proliferation
Dietary Fats / adverse effects*
Fatty Liver / genetics,  metabolism,  pathology
Gene Expression Regulation / genetics
Immediate-Early Proteins / genetics*
Intestinal Absorption / genetics
Intestinal Mucosa / metabolism,  pathology
Intestine, Small / surgery
Intestines / metabolism,  pathology,  physiopathology*
Lipid Metabolism / genetics*
Lipids / analysis,  blood
Male
Membrane Proteins / genetics*
Mice
Mice, Inbred C57BL
Mice, Knockout
RNA, Messenger / metabolism
Short Bowel Syndrome / metabolism,  pathology,  physiopathology*
Time Factors
Triglycerides / metabolism
Weight Gain / genetics*
Grant Support
ID/Acronym/Agency:
DK-56260/DK/NIDDK NIH HHS; DK46122/DK/NIDDK NIH HHS; DK50466/DK/NIDDK NIH HHS; DK56341/DK/NIDDK NIH HHS; DK61216/DK/NIDDK NIH HHS; HL-38180/HL/NHLBI NIH HHS; P30 DK52574/DK/NIDDK NIH HHS; R01 DK046122/DK/NIDDK NIH HHS
Chemical
Reg. No./Substance:
0/Dietary Fats; 0/Ifrd1 protein, mouse; 0/Immediate-Early Proteins; 0/Lipids; 0/Membrane Proteins; 0/RNA, Messenger; 0/Triglycerides
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  The eIF2 kinase GCN2 is essential for the murine immune system to adapt to amino acid deprivation by...
Next Document:  An inflection point of serum 25-hydroxyvitamin D for maximal suppression of parathyroid hormone is n...