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PMID: 17299101 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Adipocyte enhancer-binding protein 1 modulates adiposity and energy homeostasis.

Obesity (Silver Spring, Md.) ·Vol. 15 ·No. 2 ·2007-02-00 ·Pages 288-302

Ro HS, Zhang L, Majdalawieh A, Kim SW, Wu X, Lyons PJ, Webber C, Ma H, Reidy SP, Boudreau A, Miller JR, Mitchell P, McLeod RS

Abstract

To determine whether adipocyte enhancer binding protein (AEBP) 1, a transcriptional repressor that is down-regulated during adipogenesis, functions as a critical regulator of adipose tissue homeostasis through modulation of phosphatase and tensin homolog deleted on chromosome ten (PTEN) tumor suppressor activity and mitogen-activated protein kinase (MAPK) activation. We examined whether AEBP1 physically interacts with PTEN in 3T3-L1 cells by coimmunoprecipitation analysis. We generated AEBP1-null mice and examined the physiological role of AEBP1 as a key modulator of in vivo adiposity. Using adipose tissue from wild-type and AEBP1-null animals, we examined whether AEBP1 affects PTEN protein level. AEBP1 interacts with PTEN, and deficiency of AEBP1 increases adipose tissue PTEN mass. AEBP1-null mice have reduced adipose tissue mass and enhanced apoptosis with suppressed survival signal. Primary pre-adipocytes from AEBP1-null adipose tissues exhibit lower basal MAPK activity with defective proliferative potential. AEBP1-null mice are also resistant to diet-induced obesity, suggesting a regulatory role for AEBP1 in energy homeostasis. Our results suggest that AEBP1 negatively regulates adipose tissue PTEN levels, in conjunction with its role in proliferation and differentiation of pre-adipocytes, as a key functional role in modulation of in vivo adiposity.

MeSH Terms
3T3-L1 Cells Adipose Tissue, White/physiology Adiposity/genetics Animals Apoptosis Carboxypeptidases/genetics,metabolism,physiology Energy Metabolism/genetics Female Homeostasis/genetics Male Mice Mice, Inbred C57BL Mice, Knockout PTEN Phosphohydrolase/metabolism Protein Binding Protein Processing, Post-Translational Repressor Proteins/genetics,metabolism,physiology
Chemicals
Aebp1 protein, mouse Repressor Proteins PTEN Phosphohydrolase Pten protein, mouse Carboxypeptidases
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Ro Hyo-Sung
Department of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Nova Scotia, Canada. hsro@dal.ca
Zhang Lei
Majdalawieh Amin
Kim Sung-Woo
Wu Xue
Lyons Peter J
Webber Chris
Ma Hong
Reidy Shannon P
Boudreau Aaron
Miller Jessica R
Mitchell Patricia
McLeod Roger S
Article Info
Journal
Obesity (Silver Spring, Md.)
Abbr.
Obesity (Silver Spring)
ISSN
1930-7381
Published
2007-02-00
Pages
288-302
Language
English
Region
United States
NLM ID
101264860
Subset
IM
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