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Pancreatic β-cell protection from inflammatory stress by the endoplasmic reticulum proteins thrombospondin 1 and mesencephalic astrocyte-derived neutrotrophic factor (MANF)

机译:胰腺β细胞免受内质网蛋白血压出素1的炎症应激1和中脑过度星形细胞衍生中性营养因子(MANF)

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摘要

Cytokine-induced endoplasmic reticulum (ER) stress is one of the molecular mechanisms underlying pancreatic β-cell demise in type 1 diabetes. Thrombospondin 1 (THBS1) was recently shown to promote β-cell survival during lipotoxic stress. Here we show that ER-localized THBS1 is cytoprotective to rat, mouse, andhumanβ-cells exposed to cytokines or thapsigargininduced ER stress. THBS1 confers cytoprotection by maintaining expression of mesencephalic astrocyte-derived neutrotrophic factor (MANF) in β-cells and thereby prevents the BH3-only protein BIM (BCL2-interacting mediator of cell death)-dependent triggering of the mitochondrial pathway of apoptosis. Prolonged exposure ofβ-cells to cytokines or thapsigargin leads to THBS1 and MANF degradation and loss of this prosurvival mechanism. Approaches that sustain intracellular THBS1 and MANF expression in β-cells should be explored as a cytoprotective strategy in type 1 diabetes.
机译:细胞因子诱导的内质网(ER)应激是1型糖尿病患者胰腺β细胞消亡的分子机制之一。最近显示血压素素1(THBS1)在脂毒性应激期间促进β细胞存活。在这里,我们表明ER局部化的THBS1是对大鼠,小鼠,ANDHUMANβ细胞暴露于细胞因子或尾剂的抗菌的细胞保护。 Thbs1通过维持β-细胞中的脑脑过滤肌衍生的中性营养因子(MANF)的表达来赋予细胞保护,从而防止BH3蛋白BIM(BCL2相互作用的细胞死亡介质) - 依赖性凋亡的线粒体途径触发。长时间暴露于细胞因子或尾剂导致THBS1和Manf降解和这种冒失力机制的丧失。应探讨维持细胞内THBS1和β-细胞中的MANF表达的方法,作为1型糖尿病的细胞保护策略。

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