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未折叠蛋白反应在克拉伯病中被激活,其方式依赖于突变类型。

Unfolded protein response is activated in Krabbe disease in a manner dependent on the mutation type.

机构信息

Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.

Department of Pathophysiology and Metabolism, Kawasaki Medical School, Okayama, Japan.

出版信息

J Hum Genet. 2018 Jun;63(6):699-706. doi: 10.1038/s10038-018-0445-8. Epub 2018 Apr 3.

Abstract

Krabbe disease, one of the autosomal-recessive lysosomal storage disorders (LSDs), is caused by a deficiency of galactocerebrosidase (GALC) activity, resulting in the intracellular accumulation of psychosine, which is cytotoxic for neuronal cells. Genetically pathogenic mutations result in conformational changes in GALC and disrupt the lysosmal trafficking of cargos, which subsequently accumulate in the endoplasmic reticulum (ER). Recently, ER stress together with the activation of the unfolded protein response (UPR) has been suggested to play a key role in the pathogenesis of LSDs. In this study, we hence investigated whether the UPR is activated in Krabbe disease using COS-7 cells expressing pathogenic GALC mutants and skin fibroblasts (SFs) from Krabbe disease patients with various phenotypes, using a combination of semiquantitative and quantitative real-time polymerase chain reactions. We found that UPR activation in Krabbe disease depends on the mutations and cell types, and there is the possibility that multiple pathways, involving ER chaperones, inositol-requiring kinase 1, and protein kinase regulated by RNA-like ER kinase are activated by mutations associated with the infantile form. These results indicate that in Krabbe disease, each misfolded/unfolded protein evokes different UPR activation depending on the mutation, and that the activated pathways affect the phenotypes.

摘要

克拉伯病是一种常染色体隐性溶酶体贮积症(LSD),由半乳糖脑苷脂酶(GALC)活性缺乏引起,导致神经细胞内神经鞘脂积聚,从而产生细胞毒性。遗传致病性突变导致 GALC 构象改变,并破坏了溶酶体的货物运输,随后货物在内质网(ER)中积累。最近,内质网应激以及未折叠蛋白反应(UPR)的激活被认为在 LSD 的发病机制中起关键作用。在这项研究中,我们使用表达致病性 GALC 突变体的 COS-7 细胞和来自具有不同表型的克拉伯病患者的皮肤成纤维细胞(SF),结合半定量和实时定量聚合酶链反应,研究了 UPR 是否在克拉伯病中被激活。我们发现,克拉伯病中 UPR 的激活取决于突变和细胞类型,并且有可能与婴儿型相关的突变激活了涉及内质网伴侣、肌醇需求激酶 1 和 RNA 样内质网激酶调节的蛋白激酶等多种途径。这些结果表明,在克拉伯病中,每种错误折叠/未折叠的蛋白根据突变而引发不同的 UPR 激活,并且激活的途径会影响表型。

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