Chaperone-mediated autophagy degrades SERPINA1E342K/α1-antitrypsin Z variant and alleviates cell stress.

IF 14.3 Autophagy Pub Date : 2025-08-01 Epub Date: 2025-04-01 DOI:10.1080/15548627.2025.2480037
Jiayu Lin, Xinyue Wei, Yan Dai, Haorui Lu, Yajian Song, Jiansong Ju, Rihan Wu, Qichen Cao, Hao Yang, Lang Rao
{"title":"Chaperone-mediated autophagy degrades SERPINA1<sup>E342K</sup>/α1-antitrypsin Z variant and alleviates cell stress.","authors":"Jiayu Lin, Xinyue Wei, Yan Dai, Haorui Lu, Yajian Song, Jiansong Ju, Rihan Wu, Qichen Cao, Hao Yang, Lang Rao","doi":"10.1080/15548627.2025.2480037","DOIUrl":null,"url":null,"abstract":"<p><p>Chaperone-mediated autophagy (CMA) is a specific form of autophagy that selectively targets proteins containing a KFERQ-like motif and relies on the chaperone protein HSPA8/HSC70 for substrate recognition. In SERPINA1/a1-antitrypsin deficiency (AATD), a disease characterized by the hepatic buildup of the SERPINA1<sup>E342K</sup>/ATZ, CMA's role had been unclear. This work demonstrates the critical role that CMA plays in preventing SERPINA1<sup>E342K</sup>/ATZ accumulation; suppressing CMA worsens SERPINA1<sup>E342K</sup>/ATZ accumulation while activating it through chemical stimulation or LAMP2A overexpression promotes SERPINA1<sup>E342K</sup>/ATZ breakdown. Specifically, SERPINA1<sup>E342K</sup>/ATZ's <sub>121</sub>QELLR<sub>125</sub> motif is critical for HSPA8/HSC70 recognition and LAMP2A's charged C-terminal cytoplasmic tail is vital for substrate binding, facilitating CMA-mediated degradation of SERPINA1<sup>E342K</sup>/ATZ. This selective activation of CMA operates independently of other autophagy pathways and alleviates SERPINA1<sup>E342K</sup>/ATZ aggregate-induced cellular stress. In vivo administration of AR7 promotes hepatic SERPINA1<sup>E342K</sup>/ATZ elimination and mitigates hepatic SERPINA1<sup>E342K</sup>/ATZ aggregation pathology. These findings highlight CMA's critical function in cellular protein quality control of SERPINA1<sup>E342K</sup>/ATZ and place it as a novel target for AATD treatment.<b>Abbreviation:</b> AR7: atypical retinoid 7; ATG16L1: autophagy related 16 like 1; AATD: SERPINA1/alpha-1 antitrypsin deficiency; CHX: cycloheximide; CMA: chaperone-mediated autophagy; CQ: chloroquine; ER: endoplasmic reticulum; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; HSPA8/HSC70: heat shock protein family A (Hsp70) member 8; LAMP2A: lysosomal associated membrane protein 2A; LAMP2B: lysosomal associated membrane protein 2B; LAMP2C: lysosomal associated membrane protein 2C; MG132: carbobenzoxy-L-leucyl-L-leucyl-L-leucinal; PAS-D: periodic acid-Schiff plus diastase; SERPINA1/A1AT: serpin family A member 1; SERPINA1<sup>E342K</sup>/ATZ: Z variant of SERPINA1; TMRE: tetramethyl rhodamine ethyl ester perchlorate.</p>","PeriodicalId":93893,"journal":{"name":"Autophagy","volume":" ","pages":"1662-1679"},"PeriodicalIF":14.3000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12282993/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Autophagy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/15548627.2025.2480037","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/1 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Chaperone-mediated autophagy (CMA) is a specific form of autophagy that selectively targets proteins containing a KFERQ-like motif and relies on the chaperone protein HSPA8/HSC70 for substrate recognition. In SERPINA1/a1-antitrypsin deficiency (AATD), a disease characterized by the hepatic buildup of the SERPINA1E342K/ATZ, CMA's role had been unclear. This work demonstrates the critical role that CMA plays in preventing SERPINA1E342K/ATZ accumulation; suppressing CMA worsens SERPINA1E342K/ATZ accumulation while activating it through chemical stimulation or LAMP2A overexpression promotes SERPINA1E342K/ATZ breakdown. Specifically, SERPINA1E342K/ATZ's 121QELLR125 motif is critical for HSPA8/HSC70 recognition and LAMP2A's charged C-terminal cytoplasmic tail is vital for substrate binding, facilitating CMA-mediated degradation of SERPINA1E342K/ATZ. This selective activation of CMA operates independently of other autophagy pathways and alleviates SERPINA1E342K/ATZ aggregate-induced cellular stress. In vivo administration of AR7 promotes hepatic SERPINA1E342K/ATZ elimination and mitigates hepatic SERPINA1E342K/ATZ aggregation pathology. These findings highlight CMA's critical function in cellular protein quality control of SERPINA1E342K/ATZ and place it as a novel target for AATD treatment.Abbreviation: AR7: atypical retinoid 7; ATG16L1: autophagy related 16 like 1; AATD: SERPINA1/alpha-1 antitrypsin deficiency; CHX: cycloheximide; CMA: chaperone-mediated autophagy; CQ: chloroquine; ER: endoplasmic reticulum; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; HSPA8/HSC70: heat shock protein family A (Hsp70) member 8; LAMP2A: lysosomal associated membrane protein 2A; LAMP2B: lysosomal associated membrane protein 2B; LAMP2C: lysosomal associated membrane protein 2C; MG132: carbobenzoxy-L-leucyl-L-leucyl-L-leucinal; PAS-D: periodic acid-Schiff plus diastase; SERPINA1/A1AT: serpin family A member 1; SERPINA1E342K/ATZ: Z variant of SERPINA1; TMRE: tetramethyl rhodamine ethyl ester perchlorate.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
伴侣蛋白介导的自噬降解SERPINA1E342K/α1-抗胰蛋白酶Z变异,减轻细胞应激。
伴侣蛋白介导的自噬(CMA)是自噬的一种特殊形式,它选择性地针对含有 KFERQ 样基序的蛋白质,并依赖伴侣蛋白 HSPA8/HSC70 来识别底物。SERPINA1/a1-抗胰蛋白酶缺乏症(AATD)是一种以 SERPINA1E342K/ATZ 的肝脏堆积为特征的疾病,在这种疾病中,CMA 的作用一直不明确。这项研究证明了 CMA 在防止 SERPINA1E342K/ATZ 积累方面的关键作用;抑制 CMA 会加重 SERPINA1E342K/ATZ 的积累,而通过化学刺激或 LAMP2A 过表达激活 CMA 则会促进 SERPINA1E342K/ATZ 的分解。具体来说,SERPINA1E342K/ATZ 的 121QELLR125 基序对 HSPA8/HSC70 的识别至关重要,而 LAMP2A 带电荷的 C 端胞质尾部对底物结合至关重要,从而促进了 CMA 介导的 SERPINA1E342K/ATZ 降解。这种选择性激活 CMA 的作用独立于其他自噬途径,可减轻 SERPINA1E342K/ATZ 聚合体诱导的细胞压力。在体内施用 AR7 可促进肝脏 SERPINA1E342K/ATZ 的清除,减轻肝脏 SERPINA1E342K/ATZ 聚集的病理变化。这些发现突显了 CMA 在 SERPINA1E342K/ATZ 的细胞蛋白质量控制中的关键功能,并将其作为 AATD 治疗方法的新靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
文献相关原料
公司名称
产品信息
索莱宝
diastase
索莱宝
PBS
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Restricting intracellular Salmonella proliferation by coordinating p-TBK1 mediated mitophagy and xenophagy. Apoptotic bodies derived from human umbilical cord mesenchymal stem cells improve recovery from myocardial infarction in swine. PSAT1 inhibits mTORC1 activation by preventing Rag heterodimer formation in lung adenocarcinoma. Reconstitution of autophagic-like membrane tethering reveals that Atg11 can bind and cluster vesicles on cargo mimetics. Mitochondrial protein COX5B orchestrates antiviral autophagy and apoptosis to restrict SRBSDV propagation in Sogatella furcifera.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1