| Literature DB >> 31432317 |
Weiqi Yang1,2, Jingmo Xie3, Qiang Qiang4, Li Li5, Xiang Lin6, Yiqing Ren4, Wenlei Ren4, Qiong Liu1, Guomin Zhou1, Wenshi Wei4, Hexige Saiyin7, Lixiang Ma8.
Abstract
Huntington's disease (HD) is a deadly neurodegenerative disease with abnormal expansion of CAG repeats in the huntingtin gene. Mutant Huntingtin protein (mHTT) forms abnormal aggregates and intranuclear inclusions in specific neurons, resulting in cell death. Here, we tested the ability of a natural heat-shock protein 90 inhibitor, Gedunin, to degrade transfected mHTT in Neuro-2a cells and endogenous mHTT aggregates and intranuclear inclusions in both fibroblasts from HD patients and neurons derived from induced pluripotent stem cells from patients. Our data showed that Gedunin treatment degraded transfected mHTT in Neuro-2a cells, endogenous mHTT aggregates and intranuclear inclusions in fibroblasts from HD patients, and in neurons derived from induced pluripotent stem cells from patients in a dose- and time-dependent manner, and its activity depended on the proteasomal pathway rather than the autophagy route. These findings also showed that although Gedunin degraded abnormal mHTT aggregates and intranuclear inclusions in cells from HD patient, it did not affect normal cells, thus providing a new perspective for using Gedunin to treat HD.Entities:
Keywords: Degradation; Gedunin; Huntington’s disease; Mutant Huntingtin protein
Mesh:
Substances:
Year: 2019 PMID: 31432317 PMCID: PMC6864009 DOI: 10.1007/s12264-019-00421-5
Source DB: PubMed Journal: Neurosci Bull ISSN: 1995-8218 Impact factor: 5.203