Enhancement of mitochondrial biogenesis and paradoxical inhibition of lactate dehydrogenase mediated by 14‐3‐3η in oncocytomas

线粒体生物发生 生物 线粒体 乳酸脱氢酶A 糖酵解 细胞生物学 氧化磷酸化 呼吸链 线粒体呼吸链 细胞培养中氨基酸的稳定同位素标记 生物化学 新陈代谢 蛋白质组学 基因
作者
Jie Feng,Qi Zhang,Chuzhong Li,Yang Zhou,Sida Zhao,Lichuan Hong,Qi Song,Shenyuan Yu,Chunxiu Hu,Herui Wang,Chengyuan Mao,Matthew J. Shepard,Shuyu Hao,Gifty Dominah,Mitchell Sun,Hong Wan,Deric M. Park,Mark R. Gilbert,Guowang Xu,Zhengping Zhuang
标识
DOI:10.1002/path.5090
摘要

Abstract Oncocytomas represent a subset of benign pituitary adenomas that are characterized by significant mitochondrial hyperplasia. Mitochondria are key organelles for energy generation and metabolic intermediate production for biosynthesis in tumour cells, so understanding the mechanism underlying mitochondrial biogenesis and its impact on cellular metabolism in oncocytoma is vital. Here, we studied surgically resected pituitary oncocytomas by using multi‐omic analyses. Whole‐exome sequencing did not reveal any nuclear mutations, but identified several somatic mutations of mitochondrial DNA, and dysfunctional respiratory complex I. Metabolomic analysis suggested that oxidative phosphorylation was reduced within individual mitochondria, and that there was no reciprocal increase in glycolytic activity. Interestingly, we found a reduction in the cellular lactate level and reduced expression of lactate dehydrogenase A (LDHA), which contributed to mitochondrial biogenesis in an in vitro cell model. It is of note that the hypoxia‐response signalling pathway was not upregulated in pituitary oncocytomas, thereby failing to enhance glycolysis. Proteomic analysis showed that 14‐3‐3η was exclusively overexpressed in oncocytomas, and that 14‐3‐3η was capable of inhibiting glycolysis, leading to mitochondrial biogenesis in the presence of rotenone. In particular, 14‐3‐3η inhibited LDHA by direct interaction in the setting of complex I dysfunction, highlighting the role of 14‐3‐3η overexpression and inefficient oxidative phosphorylation in oncocytoma mitochondrial biogenesis. These findings deepen our understanding of the metabolic changes that occur within oncocytomas, and shine a light on the mechanism of mitochondrial biogenesis, providing a novel perspective on metabolic adaptation in tumour cells. © 2018 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

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