WFS1 is a novel component of the unfolded protein response and maintains homeostasis of the endoplasmic reticulum in pancreatic β-cells

被引:274
作者
Fonseca, SG
Fukuma, M
Lipson, KL
Nguyen, LX
Allen, JR
Oka, Y
Urano, F [1 ]
机构
[1] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[3] Tohoku Univ, Grad Sch Med, Div Mol Metab & Diabet, Sendai, Miyagi 9808575, Japan
关键词
D O I
10.1074/jbc.M507426200
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 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 glycoprotein 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.
引用
收藏
页码:39609 / 39615
页数:7
相关论文
共 38 条
  • [1] Wolfram (DIDMOAD) syndrome
    Barrett, TG
    Bundey, SE
    [J]. JOURNAL OF MEDICAL GENETICS, 1997, 34 (10) : 838 - 841
  • [2] Increased sensitivity to dextran sodium sulfate colitis in IRE1β-deficient mice
    Bertolotti, A
    Wang, XZ
    Novoa, I
    Jungreis, R
    Schlessinger, K
    Cho, JH
    West, AB
    Ron, D
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (05) : 585 - 593
  • [3] IRE1 couples endoplasmic reticulum load to secretory capacity by processing the XBP-1 mRNA
    Calfon, M
    Zeng, HQ
    Urano, F
    Till, JH
    Hubbard, SR
    Harding, HP
    Clark, SG
    Ron, D
    [J]. NATURE, 2002, 415 (6867) : 92 - 96
  • [4] EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome
    Delépine, M
    Nicolino, M
    Barrett, T
    Golamaully, M
    Lathrop, GM
    Julier, C
    [J]. NATURE GENETICS, 2000, 25 (04) : 406 - 409
  • [5] Diabetes mellitus and exocrine pancreatic dysfunction in Perk-/- mice reveals a role for translational control in secretory cell survival
    Harding, HP
    Zeng, HQ
    Zhang, YH
    Jungries, R
    Chung, P
    Plesken, H
    Sabatini, DD
    Ron, D
    [J]. MOLECULAR CELL, 2001, 7 (06) : 1153 - 1163
  • [6] Perk is essential for translational regulation and cell survival during the unfolded protein response
    Harding, HP
    Zhang, YH
    Bertolotti, A
    Zeng, HQ
    Ron, D
    [J]. MOLECULAR CELL, 2000, 5 (05) : 897 - 904
  • [7] Regulated translation initiation controls stress-induced gene expression in mammalian cells
    Harding, HP
    Novoa, I
    Zhang, YH
    Zeng, HQ
    Wek, R
    Schapira, M
    Ron, D
    [J]. MOLECULAR CELL, 2000, 6 (05) : 1099 - 1108
  • [8] Endoplasmic reticulum stress and the development of diabetes - A review
    Harding, HP
    Ron, D
    [J]. DIABETES, 2002, 51 : S455 - S461
  • [9] Transcriptional and translational control in the mammalian unfolded protein response
    Harding, HP
    Calfon, M
    Urano, F
    Novoa, I
    Ron, D
    [J]. ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2002, 18 : 575 - 599
  • [10] Mediation of TNF receptor-associated factor effector functions by apoptosis signal-regulating kinase-1 (ASK1)
    Hoeflich, KP
    Yeh, WC
    Yao, ZB
    Mak, TW
    Woodgett, JR
    [J]. ONCOGENE, 1999, 18 (42) : 5814 - 5820