Autophagy-linked FYVE protein (Alfy) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS)

被引:0
作者
Huihui Han
Wanyi Wei
Weisong Duan
Yansu Guo
Yi Li
Jie Wang
Yue Bi
Chunyan Li
机构
[1] The Second Hospital of Hebei Medical University,Department of Neurology
[2] Institute of Cardiocerebrovascular Disease,undefined
[3] Neurological Laboratory of Hebei Province,undefined
来源
In Vitro Cellular & Developmental Biology - Animal | 2015年 / 51卷
关键词
Alfy; Amyotrophic lateral sclerosis; G93A-SOD1 transgenic mouse; Cu/Zn superoxide dismutase; TDP43; Autophagy;
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学科分类号
摘要
Autophagy-linked FYVE (Alfy) is a protein implicated in the selective degradation of aggregated proteins. In our present study, we found that Alfy was recruited into the aggregated G93A-SOD1 in transgenic mice with amyotrophic lateral sclerosis (ALS). We demonstrated that Alfy overexpression could decrease the expression of mutant proteins via the autophagosome-lysosome pathway, and thereby, the toxicity of mutant proteins was reduced. The clearance of the mutant proteins in NSC34 cells was significantly inhibited in an Alfy knockdown cellular model. We therefore deduced that Alfy translocalization likely is involved in the pathogenesis of ALS. Alfy may be developed into a useful target for ALS therapy.
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页码:249 / 263
页数:14
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  • [1] An T(2014)Oxidative stress and autophagic alteration in brainstem of SOD1-G93A mouse model of ALS Mol Neurobiol 49 1435-1448
  • [2] Shi P(2005)p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death J Cell Biol 171 603-614
  • [3] Duan W(1998)Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1 Science 281 1851-1854
  • [4] Zhang S(2001)Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9 J Biol Chem 276 36337-36343
  • [5] Yuan P(1992)Neuroblastomaspinal cord (NSC) hybrid cell lines resemble developing motor neurons Dev Dyn 194 209-221
  • [6] Li Z(2004)DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4) Am J Hum Genet 74 1128-1135
  • [7] Wu D(2010)p62/SQSTM1 and ALFY interact to facilitate the formation of p62 bodies/ALIS and their degradation by autophagy Autophagy 6 330-344
  • [8] Xu Z(2006)Early reduction of NeuN antigenicity induced by soman poisoning in mice can be used to predict delayed neuronal degeneration in the hippocampus Neurosci Lett 8 37-42
  • [9] Li C(2011)Understanding the role of TDP-43 and FUS/TLS in ALS and beyond Curr Opin Neurobiol 21 904-919
  • [10] Guo Y(1993)Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase Science 261 1047-1051