4.5 Article

Pyruvate Dehydrogenase Kinase Protects Dopaminergic Neurons from Oxidative Stress in Drosophila DJ-1 Null Mutants

期刊

MOLECULES AND CELLS
卷 45, 期 7, 页码 454-464

出版社

KOREAN SOC MOLECULAR & CELLULAR BIOLOGY
DOI: 10.14348/molcells.2022.5002

关键词

DJ-1; Drosophila; oxidative stress; Parkinson's disease; pyruvate dehydrogenase kinase

资金

  1. National Research Foundation of Korea - Ministry of Science and ICT [2020R1F1A105165912, 2016R1A5A2007009]
  2. Korea Basic Science Institute (National Research Facilities and Equipment Center) - Ministry of Education [2021R1A-6C101A425]

向作者/读者索取更多资源

DJ-1 is a causative gene of early-onset familial Parkinson's disease (PD), and it influences the pathogenesis of sporadic PD by affecting reactive oxygen species (ROS) levels. PDK and PDP have been shown to play critical roles in protecting against oxidative stress by regulating glucose metabolism in the mitochondria, which is a major source of intracellular ROS.
DJ-1 is one of the causative genes of early-onset familial Parkinson's disease (PD). As a result, DJ-1 influences the pathogenesis of sporadic PD. DJ-1 has various physiological functions that converge to control the levels of intracellular reactive oxygen species (ROS). Based on genetic analyses that sought to investigate novel antioxidant DJ-1 downstream genes, pyruvate dehydrogenase (PDH) kinase (PDK) was demonstrated to increase survival rates and decrease dopaminergic (DA) neuron loss in DJ-1 mutant flies under oxidative stress. PDK phosphorylates and inhibits the PDH complex (PDC), subsequently downregulating glucose metabolism in the mitochondria, which is a major source of intracellular ROS. A loss-of-function mutation in PDK was not found to have a significant effect on fly development and reproduction, but severely ameliorated oxidative stress resistance. Thus, PDK plays a critical role in the protection against oxidative stress. Loss of PDH phosphatase (PDP), which dephosphorylates and activates PDH, was also shown to protect DJ-1 mutants from oxidative stress, ultimately supporting our findings. Further genetic analyses suggested that DJ-1 controls PDK expression through hypoxia-inducible factor 1 (HIF-1), a transcriptional regulator of the adaptive response to hypoxia and oxidative stress. Furthermore, CPI-613, an inhibitor of PDH, protected DJ-1 null flies from oxidative stress, suggesting that the genetic and pharmacological inhibition of PDH may be a novel treatment strategy for PD associated with DJ-1 dysfunction.

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