Identification of intracellular peptides in rat adipose tissue: Insights into insulin resistance


Autoria(s): Berti, Denise A.; Russo, Lilian C.; Castro, Leandro Mantovani de; Cruz, Lilian; Gozzo, Fabio C.; Heimann, Joel Claudio; Lima, Fabio Bessa; Oliveira, Ariclecio Cunha de; Sertie, Sandra Andreotti; Prada, Patrícia de Oliveira; Heimann, Andrea S.; Ferro, Emer Suavinho
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

01/11/2013

01/11/2013

2012

Resumo

Intracellular peptides generated by the proteasome and oligopeptidases have been suggested to function in signal transduction and to improve insulin resistance in mice fed a high-caloric diet. The aim of this study was to identify specific intracellular peptides in the adipose tissue of Wistar rats that could be associated with the physiological and therapeutic control of glucose uptake. Using semiquantitative mass spectrometry and LC/MS/MS analyses, we identified ten peptides in the epididymal adipose tissue of the Wistar rats; three of these peptides were present at increased levels in rats that were fed a high-caloric Western diet (WD) compared with rats fed a control diet (CD). The results of affinity chromatography suggested that in the cytoplasm of epididymal adipose tissue from either WD or CD rats, distinctive proteins bind to these peptides. However, despite the observed increase in the WD animals, the evaluated peptides increased insulin-stimulated glucose uptake in 3T3-L1 adipocytes treated with palmitate. Thus, intracellular peptides from the adipose tissue of Wistar rats can bind to specific proteins and facilitate insulin-induced glucose uptake in 3T3-L1 adipocytes.

Brazilian National Research Council (CNPq) [559698/2009-7-Rede GENO-PROT]

Brazilian National Research Council (CNPq)

University of Sao Paulo (NAPNAUSP)

University of Sao Paulo (NAPNA-USP) [2011.1.9333.1.3]

CNPq

CNPq

Sao Paulo State Research Foundation (FAPESP)

Sao Paulo State Research Foundation (FAPESP)

Identificador

PROTEOMICS, HOBOKEN, v. 12, n. 17, Special Issue, supl., Part 3, pp. 2668-2681, AUG, 2012

1615-9853

http://www.producao.usp.br/handle/BDPI/37311

10.1002/pmic.201200051

http://dx.doi.org/10.1002/pmic.201200051

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

HOBOKEN

Relação

PROTEOMICS

Direitos

closedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #ADIPOSE TISSUE #BIOMEDICINE #INSULIN RESISTANCE #OBESITY #PEPTIDE-PROTEIN INTERACTION #COA-BINDING PROTEIN #NECROSIS-FACTOR-ALPHA #MASS-SPECTROMETRY #SACCHAROMYCES-CEREVISIAE #THIMET OLIGOPEPTIDASE #3T3-L1 ADIPOCYTES #GLUCOSE-UPTAKE #INHIBITOR DBI #WILD-TYPE #KINASE-A #BIOCHEMICAL RESEARCH METHODS #BIOCHEMISTRY & MOLECULAR BIOLOGY
Tipo

article

original article

publishedVersion