NDUFA4L2减少透明细胞肾细胞癌中线粒体呼吸导致溶酶体运输缺陷。

IF 5.4 3区 材料科学 Q2 CHEMISTRY, PHYSICAL
Jaclyn M Kubala, Kristian B Laursen, Ryan Schreiner, Ryan M Williams, Johannes C van der Mijn, Michael J Crowley, Nigel P Mongan, David M Nanus, Daniel A Heller, Lorraine J Gudas
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引用次数: 0

摘要

在透明细胞肾细胞癌(ccRCC)中,缺氧信号的激活诱导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,我们之前表明这有助于ccRCC的增殖和存活。NDUFA4L2在ccRCC中的作用尚未完全阐明。NDUFA4L2被报道通过线粒体复合物I抑制来减少线粒体呼吸。我们发现NDUFA4L2在人ccRCC细胞中的表达增加了细胞外酸化率,表明糖酵解升高。相反,非癌性肾上皮细胞中NDUFA4L2的表达降低了耗氧率,同时增加了细胞外酸化率,这表明NDUFA4L2单独诱导了Warburg样效应。我们对NDUFA4L2相关复合物进行了基于质谱(MS)的蛋白质组学研究。比较RCC4-P(亲代)ccRCC细胞与其中NDUFA4L2被CRISPR-Cas9敲除的RCC4(RCC4-KO-643),我们鉴定了在NDUFA4L2免疫沉淀物中富集的3215种蛋白质。排名靠前的途径包括“癌症的代谢再编程”和“癌症的糖酵解激活(Warburg效应)”。我们还表明,NDUFA4L2增强线粒体断裂,与溶酶体相互作用,并增加线粒体与溶酶体的关联,这是通过高分辨率荧光显微镜和活细胞成像评估的。我们鉴定了161种溶酶体蛋白,包括与RCC4-P细胞中NDUFA4L2相关的尼曼-匹克病C型细胞内胆固醇转运蛋白1和2(NPC1,NPC2)。相对于RCC4 NDUFA4L2敲除细胞,RCC4-P细胞具有更大且数量减少的溶酶体。这些发现表明NDUFA4L2调节线粒体溶酶体的结合,并可能调节溶酶体的大小和丰度。因此,NDUFA4L2不仅可以调节ccRCC的线粒体功能,还可以调节溶酶体功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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

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.

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来源期刊
ACS Applied Energy Materials
ACS Applied Energy Materials Materials Science-Materials Chemistry
CiteScore
10.30
自引率
6.20%
发文量
1368
期刊介绍: ACS Applied Energy Materials is an interdisciplinary journal publishing original research covering all aspects of materials, engineering, chemistry, physics and biology relevant to energy conversion and storage. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important energy applications.
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