| Literature DB >> 25979357 |
Jae Ho Cho1, Jeong Hyang Park1, Chang Geon Chung1, Hyun-Jung Shim1, Keun Hye Jeon1, Seong-Woon Yu1, Sung Bae Lee2.
Abstract
Parkin, an E3 ubuquitin ligase associated with Parkinson's disease (PD), has recently been implicated in mediating innate immunity. However, molecular details regarding parkin-mediated immune response remain to be elucidated. Here, we identified mitochondrial TSPO-VDAC complex to genetically interact with parkin in mediating responses against infection and wound in Drosophila. The loss-of-function mutation in parkin results in defective immune response against bacterial infection. Additionally, parkin mutant larvae showed hypersensitivity against wound regardless of bacterial infection. Interestingly, the combinatorial trans-heterozygotic mutations in parkin and TSPO, or parkin and VDAC showed similar lethal tendency with parkin homozygous mutants. Furthermore, knockdown of TSPO alone also resulted in defective responses to infection and wound analogously to parkin mutants. Taken together, we propose that parkin cooperates with TSPO-VDAC complex to mediate responses against infection and wound.Entities:
Keywords: Innate immune response; Parkin; Septic injury; TSPO; VDAC (porin); Wound
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Year: 2015 PMID: 25979357 DOI: 10.1016/j.bbrc.2015.05.006
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575