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PMID: 14576179 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A transgenic mouse with a deletion in the collagenous domain of adiponectin displays elevated circulating adiponectin and improved insulin sensitivity.

Endocrinology ·Vol. 145 ·No. 1 ·2004-01-00 ·Pages 367-83

Combs TP, Pajvani UB, Berg AH, Lin Y, Jelicks LA, Laplante M, Nawrocki AR, Rajala MW, Parlow AF, Cheeseboro L, Ding YY, Russell RG, Lindemann D, Hartley A, Baker GR, Obici S, Deshaies Y, Ludgate M, Rossetti L, Scherer PE

Abstract

Adiponectin is a plasma protein expressed exclusively in adipose tissue. Adiponectin levels are linked to insulin sensitivity, but a direct effect of chronically elevated adiponectin on improved insulin sensitivity has not yet been demonstrated. We identified a dominant mutation in the collagenous domain of adiponectin that elevated circulating adiponectin values in mice by 3-fold. Adiponectinemia raised lipid clearance and lipoprotein lipase activity, and suppressed insulin-mediated endogenous glucose production. The induction of adiponectin during puberty and the sexual dimorphism in adult adiponectin values were preserved in these transgenic animals. As a result of elevated adiponectin, serum PRL values and brown adipose mass both increased. The effects on carbohydrate and lipid metabolism were associated with elevated phosphorylation of 5'-AMP-activated protein kinase in liver and elevated expression of peroxisomal proliferator-activated receptor gamma2, caveolin-1, and mitochondrial markers in white adipose tissue. These studies strongly suggest that increasing endogenous adiponectin levels has direct effects on insulin sensitivity and may induce similar physiological responses as prolonged treatment with peroxisomal proliferator-activated receptor gamma agonists.

MeSH Terms
3T3-L1 Cells Adipocytes/cytology Adiponectin Adipose Tissue/anatomy & histology,metabolism Animals Body Composition Calorimetry, Indirect Collagen/genetics Eating Female Gene Deletion Gene Expression Regulation, Developmental Glucose Clamp Technique Glucose Intolerance/metabolism Insulin Resistance Intercellular Signaling Peptides and Proteins Mice Mice, Transgenic Prolactin/blood Protein Structure, Tertiary Proteins/genetics,metabolism Receptors, Cytoplasmic and Nuclear/agonists Transcription Factors/agonists Transcription, Genetic
Chemicals
Adiponectin Intercellular Signaling Peptides and Proteins Proteins Receptors, Cytoplasmic and Nuclear Transcription Factors Prolactin Collagen
Authors & Affiliations
20 authors, click to expand affiliations / ORCID
Combs Terry P
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Pajvani Utpal B
Berg Anders H
Lin Ying
Jelicks Linda A
Laplante Mathieu
Nawrocki Andrea R
Rajala Michael W
Parlow Albert F
Cheeseboro Laurelle
Ding Yang-Yang
Russell Robert G
Lindemann Dirk
Hartley Adam
Baker Glynn R C
Obici Silvana
Deshaies Yves
Ludgate Marian
Rossetti Luciano
Scherer Philipp E
Article Info
Journal
Endocrinology
Abbr.
Endocrinology
ISSN
0013-7227
Published
2004-01-00
Epub
2003-00-23
Pages
367-83
Language
English
Region
United States
NLM ID
0375040
Subset
IM
Grants
NIDDK NIH HHS · DK-61228 · United States
NIDDK NIH HHS · R01-DK-45024 · United States
NIDDK NIH HHS · R01-DK-48321 · United States
NIDDK NIH HHS · R01-DK-55758 · United States
NEI NIH HHS · R03-EY-014935 · United States
NIDDK NIH HHS · T32-DK-07513-15 · United States
NIGMS NIH HHS · T32-GM-07288 · United States
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