Suppr超能文献

肾嗜酸细胞瘤中复合物I的缺失与溶酶体功能障碍导致的线粒体自噬缺陷有关。

The Loss of Complex I in Renal Oncocytoma Is Associated with Defective Mitophagy Due to Lysosomal Dysfunction.

作者信息

Lin Lin, Patel Neal, Fernandez-Del-Rio Lucia, Benica Cristiane, Wilde Blake, Christodoulou Eirini, Ohtake Shinji, Jeong Anhyo, Kaba Aboubacar, Matulionis Nedas, Caliliw Randy, Gai Xiaowu, Christofk Heather, Shackelford David, Shuch Brian

机构信息

Department of Urology, UCLA, 405 Hilgard Avenue, Los Angeles, CA 90095, USA.

Department of Urology, Weill Cornell Medicine, 530 East 70th Street, New York, NY 10065, USA.

出版信息

Int J Mol Sci. 2025 Aug 7;26(15):7654. doi: 10.3390/ijms26157654.

Abstract

Renal oncocytoma (RO) is a benign renal neoplasm characterized by dense accumulation of dysfunctional mitochondria possibly resulting from increased mitochondrial biogenesis and decreased mitophagy; however, the mechanisms controlling these mitochondrial changes are unclear. ROs harbor recurrent inactivating mutations in mitochondrial genes encoding the Electron Transport Chain (ETC) Complex I, and we hypothesize that Complex I loss in ROs directly impairs mitophagy. Our analysis of ROs and normal kidney (NK) tissues shows that a significant portion (8 out of 17) of ROs have mtDNA Complex I loss-of-function mutations with high variant allele frequency (>50%). ROs indeed exhibit reduced Complex I expression and activity. Analysis of the various steps of mitophagy pathway demonstrates that AMPK activation in ROs leads to induction of mitochondrial biogenesis, autophagy, and formation of autophagosomes. However, the subsequent steps involving lysosome biogenesis and function are defective, resulting in an overall inhibition of mitophagy. Inhibiting Complex I in a normal kidney cell line recapitulated the observed lysosomal and mitophagy defects. Our data suggest Complex I loss in RO results in defective mitophagy due to lysosomal loss and dysfunction.

摘要

肾嗜酸细胞瘤(RO)是一种良性肾肿瘤,其特征是功能失调的线粒体密集堆积,这可能是由于线粒体生物合成增加和线粒体自噬减少所致;然而,控制这些线粒体变化的机制尚不清楚。ROs在编码电子传递链(ETC)复合体I的线粒体基因中存在复发性失活突变,我们推测ROs中复合体I的缺失直接损害了线粒体自噬。我们对ROs和正常肾(NK)组织的分析表明,很大一部分(17个中有8个)ROs具有线粒体DNA复合体I功能丧失突变,且变异等位基因频率很高(>50%)。ROs确实表现出复合体I表达和活性降低。对线粒体自噬途径各个步骤的分析表明,ROs中的AMPK激活导致线粒体生物合成、自噬和自噬体形成的诱导。然而,随后涉及溶酶体生物合成和功能的步骤存在缺陷,导致线粒体自噬总体受到抑制。在正常肾细胞系中抑制复合体I可重现观察到的溶酶体和线粒体自噬缺陷。我们的数据表明,RO中复合体I的缺失由于溶酶体的缺失和功能障碍导致线粒体自噬缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc43/12347756/991cefc43e23/ijms-26-07654-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验