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PMID: 8330737 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Targeted expression of a toxin gene to adipose tissue: transgenic mice resistant to obesity.

Genes & development ·Vol. 7 ·No. 7B ·1993-07-00 ·Pages 1318-24

Ross SR, Graves RA, Spiegelman BM

Abstract

Obesity is characterized by increased adipose tissue mass and is often accompanied by a number of other disorders, such as diabetes, hypertension, and hyperlipidemia. To investigate the interrelationship between excessive adipose tissue mass and these associated disorders, we have attempted to reduce adiposity via targeted expression of an attenuated diphtheria toxin A chain to adipose tissue, using the 5' regulatory region of the adipocyte P2 (aP2) gene. Transgenic mice with high levels of toxin expression developed chylous ascites and died shortly after birth. Transgenic mice expressing lower levels of the transgene had normal adiposity and survived to adulthood; however, they showed a complete resistance to chemically induced obesity. Nevertheless, these animals developed hyperlipidemia equal to or greater than their nontransgenic obese littermates. Moreover, MSG-treated transgenic females were fertile, unlike their obese nontransgenic littermates. These data demonstrate the feasibility of gentle manipulation of adiposity and allow a functional dissection of obesity and its metabolic sequelae.

MeSH Terms
Adipose Tissue/metabolism Animals Diphtheria Toxin/genetics Fatty Liver/chemically induced Female Fertility/genetics Gene Expression Genes, Lethal Hyperlipidemias/chemically induced Male Mice Mice, Transgenic Obesity/genetics Peptide Fragments/genetics Sodium Glutamate/toxicity
Chemicals
Diphtheria Toxin Peptide Fragments diphtheria toxin fragment A Sodium Glutamate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ross S R
Department of Biochemistry (m/c 536), University of Illinois College of Medicine, Chicago 60612.
Graves R A
Spiegelman B M
Article Info
Journal
Genes & development
Abbr.
Genes Dev
ISSN
0890-9369
Published
1993-07-00
Pages
1318-24
Language
English
Region
United States
NLM ID
8711660
Subset
IM
Grants
NIDDK NIH HHS · DK 31405 · United States
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