https://scholars.lib.ntu.edu.tw/handle/123456789/586885
標題: | Stress-induced p53 drives BAG5 cochaperone expression to control a-synuclein aggregation in Parkinson's disease | 作者: | Chen H.-Y. CHIN-HSIEN LIN Teng S.-C. Ergun Y. Chou G.-L. Li T.-K. SHU-CHUN TENG Topcu Z. |
關鍵字: | a-synuclein; BAG5; cochaperone; p53; Parkinson's disease | 公開日期: | 2020 | 卷: | 12 | 期: | 20 | 起(迄)頁: | 20702-20718 | 來源出版物: | Aging | 摘要: | Parkinson's disease (PD) is a common neurodegenerative disorder with the pathological hallmark of a-synuclein aggregation. Dysregulation of a-synuclein homeostasis caused by aging, genetic, and environmental factors underlies the pathogenesis of PD. While chaperones are essential for proteostasis, whether modulation of cochaperones may participate in PD formation has not been fully characterized. Here, we assessed the expression of several HSP70- and HSP90-related factors under various stresses and found that BAG5 expression is distinctively elevated in etoposide- or H202-treated SH-SY5Y cells. Stress-induced p53 binds to the BAG5 promoter directly to stimulate BAG5. Induced BAG5 binds a-synuclein and HSP70 in both cell cultures and brain lysates from PD patients. Overexpressed BAG5 may result in the loss of its ability to promote HSP70. Importantly, a-synuclein aggregation in SH-SY5Y cells requires BAG5. BAG5 expression is also detected in transgenic SNCA mutant mice and in PD patients. Together, our data reveal stress-induced p53-BAG5-HSP70 regulation that provides a potential therapeutic angle for PD. ? 2020 Chen et al. |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85095861564&doi=10.18632%2faging.103998&partnerID=40&md5=97c5cb6dfaaea57d33ee510888fa34be https://scholars.lib.ntu.edu.tw/handle/123456789/586885 |
ISSN: | 19454589 | DOI: | 10.18632/aging.103998 | SDG/關鍵字: | alpha synuclein; BAG5 protein, human; protein p53; signal transducing adaptor protein; animal; cell culture; disease model; gene expression regulation; genetics; human; mouse; Parkinson disease; physiology; Adaptor Proteins, Signal Transducing; alpha-Synuclein; Animals; Cells, Cultured; Disease Models, Animal; Gene Expression Regulation; Humans; Mice; Parkinson Disease; Tumor Suppressor Protein p53 |
顯示於: | 醫學院附設醫院 (臺大醫院) |
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