The Ca2+-binding protein sorcin stimulates transcriptional activity of the unfolded protein response mediator ATF6

被引:4
|
作者
Parks, Steven Z. [1 ]
Gao, Tian [1 ,5 ]
Awuapura, Natalia Jimenez [1 ]
Ayathamattam, Joseph [1 ]
Chabosseau, Pauline L. [1 ]
Kalvakolanu, Dhananjaya, V [2 ,3 ]
Valdivia, Hector H. [4 ]
Rutter, Guy A. [1 ]
Leclerc, Isabelle [1 ]
Nakatogawa, Hitoshi
机构
[1] Imperial Coll London, Dept Metab Digest & Reprod, Sect Cell Biol & Funct Genom, London W12 0NN, England
[2] Univ Maryland, Sch Med, Dept Microbiol, Baltimore, MD 21201 USA
[3] Univ Maryland, Sch Med, Dept Immunol, Baltimore, MD 21201 USA
[4] Univ Wisconsin, Cardiovasc Res Ctr, Madison, WI USA
[5] Univ Zurich, Dept Mol Mech Dis, Zurich, Switzerland
基金
英国惠康基金;
关键词
ATF6; ER stress; lipotoxicity; sorcin; ENDOPLASMIC-RETICULUM STRESS; ER STRESS; INSULIN-RESISTANCE; CRYSTAL-STRUCTURE; CALCIUM-RELEASE; BINDING; MODULATION; ACTIVATION; PROTEOLYSIS; HOMEOSTASIS;
D O I
10.1002/1873-3468.14101
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
Sorcin is a calcium-binding protein involved in maintaining endoplasmic reticulum (ER) Ca2+ stores. We have previously shown that overexpressing sorcin under the rat insulin promoter was protective against high-fat diet-induced pancreatic beta-cell dysfunction in vivo. Activating transcription factor 6 (ATF6) is a key mediator of the unfolded protein response (UPR) that provides cellular protection during the progression of ER stress. Here, using nonexcitable HEK293 cells, we show that sorcin overexpression increased ATF6 signalling, whereas sorcin knock out caused a reduction in ATF6 transcriptional activity and increased ER stress. Altogether, our data suggest that sorcin downregulation during lipotoxic stress may prevent full ATF6 activation and a normal UPR during the progression of obesity and insulin resistance.
引用
收藏
页码:1782 / 1796
页数:15
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