Renal L-2-hydroxyglutarate dehydrogenase activity promotes hypoxia tolerance and mitochondrial metabolism in Drosophila melanogaster

IF 7 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Nader H. Mahmoudzadeh , Yasaman Heidarian , Jason P. Tourigny , Alexander J. Fitt , Katherine Beebe , Hongde Li , Arthur Luhur , Kasun Buddika , Liam Mungcal , Anirban Kundu , Robert A. Policastro , Garrett J. Brinkley , Gabriel E. Zentner , Travis Nemkov , Robert Pepin , Geetanjali Chawla , Sunil Sudarshan , Aylin R. Rodan , Angelo D'Alessandro , Jason M. Tennessen
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引用次数: 0

Abstract

Objectives

The mitochondrial enzyme L-2-hydroxyglutarate dehydrogenase (L2HGDH) regulates the abundance of L-2-hydroxyglutarate (L-2HG), a potent signaling metabolite capable of influencing chromatin architecture, mitochondrial metabolism, and cell fate decisions. Loss of L2hgdh activity in humans induces ectopic L-2HG accumulation, resulting in neurodevelopmental defects, altered immune cell function, and enhanced growth of clear cell renal cell carcinomas. To better understand the molecular mechanisms that underlie these disease pathologies, we used the fruit fly Drosophila melanogaster to investigate the endogenous functions of L2hgdh.

Methods

L2hgdh mutant adult male flies were analyzed under normoxic and hypoxic conditions using a combination of semi-targeted metabolomics and RNA-seq. These multi-omic analyses were complemented by tissue-specific genetic studies that examined the effects of L2hgdh mutations on the Drosophila renal system (Malpighian tubules; MTs).

Results

Our studies revealed that while L2hgdh is not essential for growth or viability under standard culture conditions, L2hgdh mutants are hypersensitive to hypoxia and expire during the reoxygenation phase with severe disruptions of mitochondrial metabolism. Moreover, we find that the fly renal system is a key site of L2hgdh activity, as L2hgdh mutants that express a rescuing transgene within the MTs survive hypoxia treatment and exhibit normal levels of mitochondrial metabolites. We also demonstrate that even under normoxic conditions, L2hgdh mutant MTs experience significant metabolic stress and are sensitized to aberrant growth upon Egfr activation.

Conclusions

These findings present a model in which renal L2hgdh activity limits systemic L-2HG accumulation, thus indirectly regulating the balance between glycolytic and mitochondrial metabolism, enabling successful recovery from hypoxia exposure, and ensuring renal tissue integrity.

肾脏 L-2-羟基戊二酸脱氢酶活性促进黑腹果蝇耐缺氧能力和线粒体代谢
线粒体酶 L-2-羟基戊二酸脱氢酶(L2HGDH)调节 L-2-羟基戊二酸(L-2HG)的丰度,L-2HG 是一种强效的信号代谢产物,能够影响染色质结构、线粒体代谢和细胞命运决定。人体内 L2hgdh 活性的缺失会诱导 L-2HG 的异位积累,从而导致神经发育缺陷、免疫细胞功能改变以及透明细胞肾细胞癌的生长增强。为了更好地了解这些疾病病理的分子机制,我们利用黑腹果蝇研究了L2hgdh的内源性功能。我们的研究发现,虽然在标准培养条件下,L2hgdh 对生长或存活并不重要,但 L2hgdh 突变体对缺氧不敏感,并在复氧阶段死亡,线粒体代谢受到严重破坏。此外,我们还发现苍蝇肾脏系统(Malpighian tubules; MTs)是 L2hgdh 活性的关键部位,因为在 MTs 中表达拯救转基因的 L2hgdh 突变体能在缺氧处理中存活,并表现出正常水平的线粒体代谢物。我们还证明,即使在正常缺氧条件下,L2hgdh 突变体 MT 也会经受巨大的代谢压力,并在 Egfr 激活后出现异常生长。总之,我们的研究结果提出了一个模型,在该模型中,肾脏 L2hgdh 的活性限制了全身 L-2HG 的积累,从而间接调节了糖酵解和线粒体代谢之间的平衡,使其能够从缺氧暴露中成功恢复,并确保肾脏组织的完整性。
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来源期刊
Molecular Metabolism
Molecular Metabolism ENDOCRINOLOGY & METABOLISM-
CiteScore
14.50
自引率
2.50%
发文量
219
审稿时长
43 days
期刊介绍: Molecular Metabolism is a leading journal dedicated to sharing groundbreaking discoveries in the field of energy homeostasis and the underlying factors of metabolic disorders. These disorders include obesity, diabetes, cardiovascular disease, and cancer. Our journal focuses on publishing research driven by hypotheses and conducted to the highest standards, aiming to provide a mechanistic understanding of energy homeostasis-related behavior, physiology, and dysfunction. We promote interdisciplinary science, covering a broad range of approaches from molecules to humans throughout the lifespan. Our goal is to contribute to transformative research in metabolism, which has the potential to revolutionize the field. By enabling progress in the prognosis, prevention, and ultimately the cure of metabolic disorders and their long-term complications, our journal seeks to better the future of health and well-being.
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