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常染色体显性遗传性肾小管间质性肾病-尿蛋白(ADTKD-UMOD)中内质网应激导致的线粒体失调。

Mitochondrial Dysregulation Secondary to Endoplasmic Reticulum Stress in Autosomal Dominant Tubulointerstitial Kidney Disease - UMOD (ADTKD-UMOD).

机构信息

Chair for Molecular Animal Breeding and Biotechnology, Gene Center, Ludwig-Maximilians-Universität München, D-81377 Munich, Germany.

Laboratory for Functional Genome Analysis (LAFUGA), Gene Center, Ludwig-Maximilians-Universität München, D-81377 Munich, Germany.

出版信息

Sci Rep. 2017 Feb 21;7:42970. doi: 10.1038/srep42970.

Abstract

'Autosomal dominant tubulointerstitial kidney disease - UMOD' (ADTKD-UMOD) is caused by impaired maturation and secretion of mutant uromodulin (UMOD) in thick ascending limb of Henle loop (TAL) cells, resulting in endoplasmic reticulum (ER) stress and unfolded protein response (UPR). To gain insight into pathophysiology, we analysed proteome profiles of TAL-enriched outer renal medulla samples from ADTKD-UMOD and control mice by quantitative LC-MS/MS. In total, 212 differentially abundant proteins were identified. Numerous ER proteins, including BiP (HSPA5), phosphorylated eIF2α (EIF2S1), ATF4, ATF6 and CHOP (DDIT3), were increased abundant, consistent with UPR. The abundance of hypoxia-inducible proteins with stress survival functions, i.e. HYOU1, TXNDC5 and ERO1L, was also increased. TAL cells in ADTKD-UMOD showed a decreased proportion of mitochondria and reduced abundance of multiple mitochondrial proteins, associated with disturbed post-translational processing and activation of the mitochondrial transcription factor NRF1. Impaired fission of organelles, as suggested by reduced abundance of FIS1, may be another reason for disturbed biogenesis of mitochondria and peroxisomes. Reduced amounts of numerous proteins of the OXPHOS and citrate cycle pathways, and activation of the LKB1-AMPK-pathway, a sensor pathway of cellular energy deficits, suggest impaired energy homeostasis. In conclusion, our study revealed secondary mitochondrial dysfunction in ADTKD-UMOD.

摘要

常染色体显性遗传性肾小管间质性肾病-尿调蛋白(ADTKD-UMOD)是由突变尿调蛋白(UMOD)在Henle 袢升支粗段(TAL)细胞中的成熟和分泌受损引起的,导致内质网(ER)应激和未折叠蛋白反应(UPR)。为了深入了解病理生理学,我们通过定量 LC-MS/MS 分析了 ADTKD-UMOD 和对照小鼠 TAL 丰富的外肾髓质样本的蛋白质组谱。总共鉴定出 212 个差异丰富的蛋白质。大量 ER 蛋白,包括 BiP(HSPA5)、磷酸化的 eIF2α(EIF2S1)、ATF4、ATF6 和 CHOP(DDIT3),丰度增加,与 UPR 一致。具有应激生存功能的缺氧诱导蛋白,即 HYOU1、TXNDC5 和 ERO1L 的丰度也增加。ADTKD-UMOD 中的 TAL 细胞显示出线粒体比例降低,多种线粒体蛋白丰度降低,与翻译后加工和线粒体转录因子 NRF1 的激活受到干扰有关。细胞器分裂减少,如 FIS1 丰度降低所表明的,可能是线粒体和过氧化物酶体生物发生受到干扰的另一个原因。许多 OXPHOS 和柠檬酸循环途径的蛋白质以及 LKB1-AMPK 途径的激活,LKB1-AMPK 途径是细胞能量不足的传感器途径,提示能量稳态受损。总之,我们的研究揭示了 ADTKD-UMOD 中的继发性线粒体功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca5/5318959/43534ae56fb9/srep42970-f1.jpg

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