Resistin is co-secreted with adiponectin in white mouse adipocytes

被引:12
作者
Musovic, Saliha [1 ]
Shrestha, Man Mohan [1 ]
Komai, Ali M. [1 ]
Olofsson, Charlotta S. [1 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Dept Physiol Metab Physiol, Med Regatan 11, SE-40530 Gothenburg, Sweden
基金
英国医学研究理事会; 瑞典研究理事会;
关键词
Resistin secretion; Mouse adipocytes; Adrenergic signalling; Diet-induced obesity; Adiponectin; Epac; EXOCYTOSIS; OBESITY; LEPTIN; CALCIUM;
D O I
10.1016/j.bbrc.2020.11.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the current work we have investigated the cellular and molecular regulation of resistin secretion in cultured and primary mouse adipocytes. Resistin is an adipose tissue hormone proposed to contribute to metabolic disease. In rodents, resistin is secreted from white adipocytes whereas it is in humans synthesised and released from other cell types within white adipose tissue. The metabolic importance of resistin has been studied in both mouse and man, but the regulation of its release remains poorly investigated. Here we define that, in mouse adipocytes, resistin secretion is triggered by an intracellular elevation of cAMP and/or Ca2+. Resistin release is stimulated via activation of beta 3 adrenergic receptors (beta(3)ARs) and the downstream signalling protein exchange protein activated by cAMP (Epac). The secretion of resistin is markedly abrogated in adipocytes isolated from obese and diabetic mice. Immunocytochemical staining demonstrates a significant overlap between signals for resistin and the adipocyte hormone adiponectin. Our data propose that resistin and adiponectin are contained within the same vesicles in mouse adipocytes and that the two hormones are co-secreted in response to the same exocytosis-triggering signals. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:707 / 713
页数:7
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