Fonseca Sonya G, Fukuma Mariko, Lipson Kathryn L, Nguyen Linh X, Allen Jenny R, Oka Yoshitomo, Urano Fumihiko
Program in Gene Function and Expression, University of Massachusetts Medical School, Worcester, Massachusetts 01605-2324, USA.
J Biol Chem. 2005 Nov 25;280(47):39609-15. doi: 10.1074/jbc.M507426200. Epub 2005 Sep 29.
In Wolfram syndrome, a rare form of juvenile diabetes, pancreatic beta-cell death is not accompanied by an autoimmune response. Although it has been reported that mutations in the WFS1 gene are responsible for the development of this syndrome, the precise molecular mechanisms underlying beta-cell death caused by the WFS1 mutations remain unknown. Here we report that WFS1 is a novel component of the unfolded protein response and has an important function in maintaining homeostasis of the endoplasmic reticulum (ER) in pancreatic beta-cells. WFS1 encodes a transmembrane glyco-protein in the ER. WFS1 mRNA and protein are induced by ER stress. The expression of WFS1 is regulated by inositol requiring 1 and PKR-like ER kinase, central regulators of the unfolded protein response. WFS1 is normally up-regulated during insulin secretion, whereas inactivation of WFS1 in beta-cells causes ER stress and beta-cell dysfunction. These results indicate that the pathogenesis of Wolfram syndrome involves chronic ER stress in pancreatic beta-cells caused by the loss of function of WFS1.
在一种罕见的青少年糖尿病——沃夫勒姆综合征中,胰腺β细胞死亡并不伴有自身免疫反应。虽然有报道称WFS1基因的突变是导致该综合征的原因,但WFS1突变引起β细胞死亡的确切分子机制仍不清楚。在此,我们报告WFS1是未折叠蛋白反应的一个新组分,并且在维持胰腺β细胞内质网(ER)的稳态中具有重要功能。WFS1在内质网中编码一种跨膜糖蛋白。WFS1的mRNA和蛋白受内质网应激诱导。WFS1的表达受未折叠蛋白反应的核心调节因子肌醇需求酶1和蛋白激酶R样内质网激酶调控。WFS1在胰岛素分泌过程中通常会上调,而β细胞中WFS1的失活会导致内质网应激和β细胞功能障碍。这些结果表明,沃夫勒姆综合征的发病机制涉及因WFS1功能丧失导致的胰腺β细胞慢性内质网应激。