Lu Wenjun, Hagiwara Daisuke, Morishita Yoshiaki, Tochiya Masayoshi, Azuma Yoshinori, Suga Hidetaka, Goto Motomitsu, Banno Ryoichi, Sugimura Yoshihisa, Oyadomari Seiichi, Mori Kazutoshi, Arima Hiroshi
Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
Neurosci Lett. 2016 Jan 26;612:199-203. doi: 10.1016/j.neulet.2015.12.031. Epub 2015 Dec 18.
Recent studies suggest that endoplasmic reticulum (ER) stress in the hypothalamus could affect systemic homeostatic regulation in areas such as energy and water balance. Activating transcription factor 6α (ATF6α) is an ER stress transducer which increases the expression of ER chaperones and ER-associated degradation (ERAD) components under ER stress. In the present study, we examined the regulation of the unfolding protein response (UPR) in mouse hypothalamic cultures of wild-type (WT) and ATF6α(-/-) mice. Thapsigargin (TG), an ER stressor, significantly increased the mRNA expression of immunoglobulin heavy chain binding protein (BiP), spliced X-box binding protein 1 (XBP1), activating transcription factor 4 (ATF4), C/EBP homologous protein (CHOP), and ERAD components, in hypothalamic cultures of WT mice with the same threshold (0.1μM) and similar time courses. On the other hand, TG-induced upregulation of BiP and CHOP as well as most ERAD-related genes, but not spliced XBP1 or ATF4, was attenuated in ATF6α(-/-) mice compared with WT mice. Our data suggest that all the UPR arms are activated similarly in the mouse hypothalamus under ER stress conditions, where ATF6α regulates the expression of ER chaperones, CHOP, and ERAD components.
最近的研究表明,下丘脑内质网(ER)应激可能会影响能量和水平衡等方面的全身稳态调节。激活转录因子6α(ATF6α)是一种ER应激转导蛋白,在ER应激条件下可增加ER伴侣蛋白和ER相关降解(ERAD)组分的表达。在本研究中,我们检测了野生型(WT)和ATF6α基因敲除(-/-)小鼠下丘脑培养物中未折叠蛋白反应(UPR)的调节情况。内质网应激诱导剂毒胡萝卜素(TG)能显著增加WT小鼠下丘脑培养物中免疫球蛋白重链结合蛋白(BiP)、剪接型X盒结合蛋白1(XBP1)、激活转录因子4(ATF4)、C/EBP同源蛋白(CHOP)以及ERAD组分的mRNA表达,其阈值相同(0.1μM)且时间进程相似。另一方面,与WT小鼠相比,TG诱导的BiP和CHOP以及大多数ERAD相关基因的上调在ATF6α(-/-)小鼠中减弱,但剪接型XBP1或ATF4未受影响。我们的数据表明,在ER应激条件下,小鼠下丘脑的所有UPR分支均以相似的方式被激活,其中ATF6α调节ER伴侣蛋白、CHOP和ERAD组分的表达。