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Important mitochondrial proteins in human omental adipose tissue show reduced expression in obesity.

Authors :
Lindinger PW
Christe M
Eberle AN
Kern B
Peterli R
Peters T
Jayawardene KJ
Fearnley IM
Walker JE
Source :
Journal of proteomics [J Proteomics] 2015 Jun 21; Vol. 124, pp. 79-87. Date of Electronic Publication: 2015 Apr 10.
Publication Year :
2015

Abstract

Impaired mitochondrial function is important in obesity and the development of insulin resistance and diabetes. The aim of this study was to identify human adipocyte-derived mitochondrial proteins associated with obesity. Mitochondrial proteins from 20 abdominal omental adipose tissue biopsies (13 obese and 7 control subjects) were separated by anion-exchange chromatography coupled to SDS-PAGE. Protein contents were compared and identified by MALDI-TOF-TOF mass spectrometry. Proteins of interest were validated, verified and quantified using immuno dot blot assays in a total of 76 mitochondrial preparations from both obese and non-obese patients. Mass spectrometric comparison of 20 mitochondrial proteomes yielded 62 proteins that were differentially expressed in adipose tissue of obese subjects. The immunological quantification of 12 mitochondrial proteins from 76 omental adipose tissue biopsies revealed four proteins, citrate synthase, HADHA, LETM1 and mitofilin inversely being associated with BMI, and mitofilin being inversely correlated with gender.<br />Biological Significance: The finding that obese human subjects have reduced levels of important mitochondrial proteins in adipocytes of omental adipose tissue as compared to non-obese controls gives new insights in the impairment of mitochondrial function in this specialized compartment of human adipose tissue in obesity and may eventually lead to the definition of valuable obesity markers.<br /> (Copyright © 2015 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1876-7737
Volume :
124
Database :
MEDLINE
Journal :
Journal of proteomics
Publication Type :
Academic Journal
Accession number :
25865306
Full Text :
https://doi.org/10.1016/j.jprot.2015.03.037