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NDUFA4L2可降低线粒体呼吸作用,导致透明细胞肾细胞癌中的溶酶体运输功能缺陷。

NDUFA4L2 reduces mitochondrial respiration resulting in defective lysosomal trafficking in clear cell renal cell carcinoma.

作者信息

Kubala Jaclyn M, Laursen Kristian B, Schreiner Ryan, Williams Ryan M, van der Mijn Johannes C, Crowley Michael J, Mongan Nigel P, Nanus David M, Heller Daniel A, Gudas Lorraine J

机构信息

Department of Pharmacology, Weill Cornell Medicine, New York, NY, USA.

Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

出版信息

Cancer Biol Ther. 2023 Dec 31;24(1):2170669. doi: 10.1080/15384047.2023.2170669.

Abstract

In clear cell renal cell carcinoma (ccRCC), activation of hypoxic signaling induces NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 4-like 2 (NDUFA4L2) expression. Over 90% of ccRCCs exhibit overexpression of NDUFA4L2, which we previously showed contributes to ccRCC proliferation and survival. The function of NDUFA4L2 in ccRCC has not been fully elucidated. NDUFA4L2 was reported to reduce mitochondrial respiration via mitochondrial complex I inhibition. We found that NDUFA4L2 expression in human ccRCC cells increases the extracellular acidification rate, indicative of elevated glycolysis. Conversely, NDUFA4L2 expression in non-cancerous kidney epithelial cells decreases oxygen consumption rate while increasing extracellular acidification rate, suggesting that a Warburg-like effect is induced by NDUFA4L2 alone. We performed mass-spectrometry (MS)-based proteomics of NDUFA4L2 associated complexes. Comparing RCC4-P (parental) ccRCC cells with RCC4 in which NDUFA4L2 is knocked out by CRISPR-Cas9 (RCC4-KO-643), we identified 3,215 proteins enriched in the NDUFA4L2 immunoprecipitates. Among the top-ranking pathways were "Metabolic Reprogramming in Cancer" and "Glycolysis Activation in Cancer (Warburg Effect)." We also show that NDUFA4L2 enhances mitochondrial fragmentation, interacts with lysosomes, and increases mitochondrial-lysosomal associations, as assessed by high-resolution fluorescence microscopy and live cell imaging. We identified 161 lysosomal proteins, including Niemann-Pick Disease Type C Intracellular Cholesterol Transporters 1 and 2 (NPC1, NPC2), that are associated with NDUFA4L2 in RCC4-P cells. RCC4-P cells have larger and decreased numbers of lysosomes relative to RCC4 NDUFA4L2 knockout cells. These findings suggest that NDUFA4L2 regulates mitochondrial-lysosomal associations and potentially lysosomal size and abundance. Consequently, NDUFA4L2 may regulate not only mitochondrial, but also lysosomal functions in ccRCC.

摘要

在透明细胞肾细胞癌(ccRCC)中,缺氧信号的激活会诱导烟酰胺腺嘌呤二核苷酸(NADH)脱氢酶(泛醌)1α亚复合体4样2(NDUFA4L2)的表达。超过90%的ccRCC表现出NDUFA4L2的过表达,我们之前的研究表明,这有助于ccRCC的增殖和存活。NDUFA4L2在ccRCC中的功能尚未完全阐明。据报道,NDUFA4L2通过抑制线粒体复合体I来降低线粒体呼吸作用。我们发现,人ccRCC细胞中NDUFA4L2的表达会提高细胞外酸化率,这表明糖酵解增强。相反,非癌性肾上皮细胞中NDUFA4L2的表达会降低耗氧率,同时提高细胞外酸化率,这表明单独的NDUFA4L2会诱导类似瓦伯格效应。我们对与NDUFA4L2相关的复合体进行了基于质谱(MS)的蛋白质组学分析。将RCC4-P(亲本)ccRCC细胞与通过CRISPR-Cas9敲除NDUFA4L2的RCC4细胞(RCC4-KO-643)进行比较,我们鉴定出3215种在NDUFA4L2免疫沉淀中富集的蛋白质。排名靠前的通路包括“癌症中的代谢重编程”和“癌症中的糖酵解激活(瓦伯格效应)”。我们还表明,通过高分辨率荧光显微镜和活细胞成像评估,NDUFA4L2会增强线粒体碎片化,与溶酶体相互作用,并增加线粒体与溶酶体的关联。我们鉴定出161种溶酶体蛋白,包括尼曼-匹克病C型细胞内胆固醇转运蛋白1和2(NPC1、NPC2),它们在RCC4-P细胞中与NDUFA4L2相关。相对于RCC4 NDUFA4L2敲除细胞,RCC4-P细胞的溶酶体更大且数量减少。这些发现表明,NDUFA4L2调节线粒体与溶酶体的关联,并可能调节溶酶体的大小和丰度。因此,NDUFA4L2可能不仅调节ccRCC中的线粒体功能,还调节溶酶体功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/279d/9897797/e856d0b42312/KCBT_A_2170669_F0001_OC.jpg

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