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限制ER相关的降解能力会对胰岛素生物合成产生急性和慢性影响
Anoop Arunagiri1, Leena Haataja1, Maroof Alam1
1Division of Metabolism, Endocrinology & Diabetes, University of Michigan Medical Center, Ann Arbor, United States of America.
胰腺β细胞HRD1降解了错误折叠的亲胰岛素. 它的缺乏会增加错误折叠的亲胰岛素,激活压力反应,降低胰岛素水平,从而导致糖尿病.
科学领域:
- 内分泌学 在内分泌学.
- 细胞生物学 细胞生物学
- 代谢疾病 代谢疾病
背景情况:
- 错误折叠的益胰岛素通过胰腺β细胞的HRD1/SEL1L被ERAD降解.
- 人们对HRD1在胰岛素生物生成中的作用进行了辩论,关于ERAD缺乏效应的报道相互矛盾.
研究的目的:
- 研究HRD1在β细胞前胰岛素稳定和糖尿病发展中的作用.
- 为了研究慢性HRD1缺乏和急性HRD1抑制在β细胞中的后果.
主要方法:
- 为慢性缺陷研究生成β细胞特异的Hrd1-KO小鼠.
- 用HRD1抑制剂急性治疗动物和人类β细胞.
- 使用生物化学标记物,电子显微镜,并评估了亲胰岛素水平和合成.
主要成果:
- Hrd1-KO小鼠患上糖尿病,显示总益胰岛素降低,但ER中错误折叠的益胰岛素增加.
- 观察到上调ER压力,自标志物,ER扩大和减少胰岛素颗粒.
- 急性HRD1抑制增加了错误折叠的亲胰岛素,激活了压力通路 (-eIF2ɑ),并诱导了自 (LC3b-II).
结论:
- HRD1调解了错误折叠的亲胰岛素分子的一个子集的处置.
- HRD1缺乏导致错误折叠的亲胰岛素积累,ER压力,抑制合成和自激活.
- 这些事件最终会降低β细胞的益胰岛素/胰岛素水平,导致糖尿病发病.
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