Analysis of neuronal phosphoproteome reveals PINK1 regulation of BAD function and cell death

  • Huida Wan
  • , Bin Tang*
  • , Xun Liao
  • , Qiufang Zeng
  • , Zhuohua Zhang
  • , Lujian Liao
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

Abstract

PINK1 mutations that disrupt its kinase activity cause autosomal recessive early onset Parkinson's disease (PD). Although research in recent years has elucidated a PINK1-Parkin pathway of mitophagy activation that requires PINK1 kinase activity, mitophagy-independent functions of PINK1 and their possible roles in PD pathogenesis have been proposed. Using an unbiased quantitative mass spectrometry approach to analyze the phosphoproteome in primary neurons from wild type and Pink1 knockout mice after mitochondrial depolarization, we uncovered PINK1-regulated phosphorylation sites, which involve coordinated activation of multiple signaling pathways that control cellular response to stress. We further identified the pro-apoptotic protein BAD as a potential mitochondrial substrate of PINK1 both in vitro and in vivo, and found that cells more susceptible to a12poptosis induced by mitochondrial damage can be rescued by phosphorylation mimic BAD. Our results thus suggest that PINK1 kinase activity is important for pro-apoptotic protein function in regulation of cell death.

Original languageEnglish
Pages (from-to)904-917
Number of pages14
JournalCell Death and Differentiation
Volume25
Issue number5
DOIs
StatePublished - 1 May 2018
Externally publishedYes

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