BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage

Loss-of-function mutations in gene encoding DJ-1 contribute to the pathogenesis of autosomal recessive early-onset familial forms of Parkinson’s disease (PD). DJ-1 is a multifunctional protein and plays a protective role against oxidative stress-induced mitochondrial damage and cell death, but the e...

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Veröffentlicht in:Oxidative medicine and cellular longevity 2017-01, Vol.2017 (2017), p.1-10
Hauptverfasser: Tang, Bei-sha, Tan, Li-ming, Wang, Chun-yu, Shen, Xiang-min, Jiang, Bo, Tang, Jian-guang, Lu, Jia-Hong, Rizwana, Kousar, Zhang, Hai-nan, Tan, Jieqiong, Qin, Li-xia, Guo, Ji-feng
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Sprache:eng
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Zusammenfassung:Loss-of-function mutations in gene encoding DJ-1 contribute to the pathogenesis of autosomal recessive early-onset familial forms of Parkinson’s disease (PD). DJ-1 is a multifunctional protein and plays a protective role against oxidative stress-induced mitochondrial damage and cell death, but the exact mechanism underlying this is not yet clearly understood. Here, using coimmunoprecipitation (Co-IP) and immunofluorescence methods, we prove that Bcl-2-associated athanogene 5 (BAG5), a BAG family member, interacts with DJ-1 in mammalian cells. Moreover, we show that BAG5 could decrease stability of DJ-1 and weaken its role in mitochondrial protection probably by influencing dimerization in stress condition. Our study reveals the relationship of BAG5 and DJ-1 suggesting a potential role for BAG5 in the pathogenesis of PD through its functional interactions with DJ-1.
ISSN:1942-0900
1942-0994
DOI:10.1155/2017/5094934