Selective removal of misfolded SOD1 delays disease onset in a mouse model of amyotrophic lateral sclerosis

作者全名："Guan, Teng; Zhou, Ting; Zhang, Xiaosha; Guo, Ying; Yang, Chaoxian; Lin, Justin; Zhang, Jiasi Vicky; Cheng, Yongquan; Marzban, Hassan; Wang, Yu Tian; Kong, Jiming"

作者地址："[Guan, Teng; Zhou, Ting; Zhang, Xiaosha; Guo, Ying; Yang, Chaoxian; Lin, Justin; Zhang, Jiasi Vicky; Cheng, Yongquan; Marzban, Hassan; Kong, Jiming] Univ Manitoba, Max Rady Coll Med, Dept Human Anat & Cell Sci, Winnipeg, MB, Canada; [Zhou, Ting] Chongqing Med Univ, Affiliated Hosp 2, Dept Pharm, Chongqing, Peoples R China; [Guo, Ying] Hebei North Univ, Dept Forens Med, Zhangjiakou, Peoples R China; [Yang, Chaoxian] Southwest Med Univ, Dept Neurobiol, Luzhou, Peoples R China; [Wang, Yu Tian] Univ British Columbia, Vancouver Coastal Hlth Res Inst, Brain Res Ctr, Vancouver, BC, Canada; [Wang, Yu Tian] Univ British Columbia, Vancouver Coastal Hlth Res Inst, Dept Med, Vancouver, BC, Canada; [Kong, Jiming] Univ Manitoba, Max Rady Coll Med, Dept Human Anat & Cell Sci, 745 Bannatyne Ave, Winnipeg, MB R3E 0J9, Canada"

通信作者："Kong, JM (通讯作者)，Univ Manitoba, Max Rady Coll Med, Dept Human Anat & Cell Sci, Winnipeg, MB, Canada.; Kong, JM (通讯作者)，Univ Manitoba, Max Rady Coll Med, Dept Human Anat & Cell Sci, 745 Bannatyne Ave, Winnipeg, MB R3E 0J9, Canada."

来源：CELLULAR AND MOLECULAR LIFE SCIENCES

ESI学科分类：MOLECULAR BIOLOGY & GENETICS

WOS号：WOS:001153163700001

JCR分区：Q1

影响因子：6.2

年份：2023

卷号：80

期号：10

开始页：　

结束页：　

文献类型：Article

关键词：Amyotrophic lateral sclerosis; Misfolded SOD1; Protein degradation; Chaperone-mediated autophagy; Lysosome

摘要："BackgroundAmyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease. There is no cure currently. The discovery that mutations in the gene SOD1 are a cause of ALS marks a breakthrough in the search for effective treatments for ALS. SOD1 is an antioxidant that is highly expressed in motor neurons. Human SOD1 is prone to aberrant modifications. Familial ALS-linked SOD1 variants are particularly susceptible to aberrant modifications. Once modified, SOD1 undergoes conformational changes and becomes misfolded. This study aims to determine the effect of selective removal of misfolded SOD1 on the pathogenesis of ALS.MethodsBased on the chaperone-mediated protein degradation pathway, we designed a fusion peptide named CT4 and tested its efficiency in knocking down intracellularly misfolded SOD1 and its efficacy in modifying the pathogenesis of ALS.ResultsExpression of the plasmid carrying the CT4 sequence in human HEK cells resulted in robust removal of misfolded SOD1 induced by serum deprivation. Co-transfection of the CT4 and the G93A-hSOD1 plasmids at various ratios demonstrated a dose-dependent knockdown efficiency on G93A-hSOD1, which could be further increased when misfolding of SOD1 was enhanced by serum deprivation. Application of the full-length CT4 peptide to primary cultures of neurons expressing the G93A variant of human SOD1 revealed a time course of the degradation of misfolded SOD1; misfolded SOD1 started to decrease by 2 h after the application of CT4 and disappeared by 7 h. Intravenous administration of the CT4 peptide at 10 mg/kg to the G93A-hSOD1 reduced human SOD1 in spinal cord tissue by 68% in 24 h and 54% in 48 h in presymptomatic ALS mice. Intraperitoneal administration of the CT4 peptide starting from 60 days of age significantly delayed the onset of ALS and prolonged the lifespan of the G93A-hSOD1 mice.ConclusionsThe CT4 peptide directs the degradation of misfolded SOD1 in high efficiency and specificity. Selective removal of misfolded SOD1 significantly delays the onset of ALS, demonstrating that misfolded SOD1 is the toxic form of SOD1 that causes motor neuron death. The study proves that selective removal of misfolded SOD1 is a promising treatment for ALS."

基金机构：The authors would like to acknowledge the assistance of Dr Lynda Kong in editing the manuscript.

基金资助正文：The authors would like to acknowledge the assistance of Dr Lynda Kong in editing the manuscript.