• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

脊髓性肌萎缩症中的自噬:从致病机制到治疗方法

Autophagy in spinal muscular atrophy: from pathogenic mechanisms to therapeutic approaches.

作者信息

Rashid Saman, Dimitriadi Maria

机构信息

School of Life and Medical Science, University of Hertfordshire, Hatfield, United Kingdom.

出版信息

Front Cell Neurosci. 2024 Jan 8;17:1307636. doi: 10.3389/fncel.2023.1307636. eCollection 2023.

DOI:10.3389/fncel.2023.1307636
PMID:38259504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10801191/
Abstract

Spinal muscular atrophy (SMA) is a devastating neuromuscular disorder caused by the depletion of the ubiquitously expressed survival motor neuron (SMN) protein. While the genetic cause of SMA has been well documented, the exact mechanism(s) by which SMN depletion results in disease progression remain elusive. A wide body of evidence has highlighted the involvement and dysregulation of autophagy in SMA. Autophagy is a highly conserved lysosomal degradation process which is necessary for cellular homeostasis; defects in the autophagic machinery have been linked with a wide range of neurodegenerative disorders, including amyotrophic lateral sclerosis, Alzheimer's disease and Parkinson's disease. The pathway is particularly known to prevent neurodegeneration and has been suggested to act as a neuroprotective factor, thus presenting an attractive target for novel therapies for SMA patients. In this review, (a) we provide for the first time a comprehensive summary of the perturbations in the autophagic networks that characterize SMA development, (b) highlight the autophagic regulators which may play a key role in SMA pathogenesis and (c) propose decreased autophagic flux as the causative agent underlying the autophagic dysregulation observed in these patients.

摘要

脊髓性肌萎缩症(SMA)是一种严重的神经肌肉疾病,由普遍表达的生存运动神经元(SMN)蛋白缺失引起。虽然SMA的遗传病因已有充分记载,但SMN缺失导致疾病进展的确切机制仍不清楚。大量证据表明自噬在SMA中存在参与和失调。自噬是一种高度保守的溶酶体降解过程,对细胞内稳态至关重要;自噬机制的缺陷与多种神经退行性疾病有关,包括肌萎缩侧索硬化症、阿尔茨海默病和帕金森病。该途径尤其以预防神经退行性变而闻名,并被认为是一种神经保护因子,因此为SMA患者的新疗法提供了一个有吸引力的靶点。在本综述中,(a)我们首次全面总结了表征SMA发展的自噬网络中的扰动,(b)强调了可能在SMA发病机制中起关键作用的自噬调节因子,(c)提出自噬通量降低是这些患者自噬失调的潜在致病因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f48/10801191/78d8fbdb05f3/fncel-17-1307636-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f48/10801191/a91a190381e7/fncel-17-1307636-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f48/10801191/e524aefd3bf3/fncel-17-1307636-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f48/10801191/a809cf620d7c/fncel-17-1307636-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f48/10801191/78d8fbdb05f3/fncel-17-1307636-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f48/10801191/a91a190381e7/fncel-17-1307636-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f48/10801191/e524aefd3bf3/fncel-17-1307636-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f48/10801191/a809cf620d7c/fncel-17-1307636-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f48/10801191/78d8fbdb05f3/fncel-17-1307636-g004.jpg

相似文献

1
Autophagy in spinal muscular atrophy: from pathogenic mechanisms to therapeutic approaches.脊髓性肌萎缩症中的自噬:从致病机制到治疗方法
Front Cell Neurosci. 2024 Jan 8;17:1307636. doi: 10.3389/fncel.2023.1307636. eCollection 2023.
2
Survival motor neuron protein reduction deregulates autophagy in spinal cord motoneurons in vitro.存活运动神经元蛋白减少会使体外脊髓运动神经元中的自噬失调。
Cell Death Dis. 2013 Jun 20;4(6):e686. doi: 10.1038/cddis.2013.209.
3
Autophagy dysregulation in cell culture and animals models of spinal muscular atrophy.脊髓性肌萎缩症细胞培养和动物模型中的自噬失调
Mol Cell Neurosci. 2014 Jul;61:133-40. doi: 10.1016/j.mcn.2014.06.006. Epub 2014 Jun 28.
4
Spinal Muscular Atrophy autophagy profile is tissue-dependent: differential regulation between muscle and motoneurons.脊髓性肌萎缩症自噬谱具有组织依赖性:肌肉和运动神经元之间的差异调节。
Acta Neuropathol Commun. 2021 Jul 3;9(1):122. doi: 10.1186/s40478-021-01223-5.
5
Therapy development for spinal muscular atrophy: perspectives for muscular dystrophies and neurodegenerative disorders.脊髓性肌萎缩症的治疗进展:对肌肉萎缩症和神经退行性疾病的展望
Neurol Res Pract. 2022 Jan 4;4(1):2. doi: 10.1186/s42466-021-00162-9.
6
Spinal motor neuron loss occurs through a p53-and-p21-independent mechanism in the Smn mouse model of spinal muscular atrophy.脊髓运动神经元的丧失是通过脊髓性肌萎缩症 Smn 小鼠模型中的 p53 和 p21 非依赖性机制发生的。
Exp Neurol. 2021 Mar;337:113587. doi: 10.1016/j.expneurol.2020.113587. Epub 2020 Dec 28.
7
Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy mice.脊髓性肌萎缩症小鼠骨骼肌中 Tweak 和 Fn14 的失调。
Skelet Muscle. 2022 Jul 28;12(1):18. doi: 10.1186/s13395-022-00301-z.
8
Modelling motor neuron disease in fruit flies: Lessons from spinal muscular atrophy.在果蝇中模拟运动神经元疾病:来自脊髓性肌肉萎缩症的启示。
J Neurosci Methods. 2018 Dec 1;310:3-11. doi: 10.1016/j.jneumeth.2018.04.003. Epub 2018 Apr 9.
9
Chronic treatment with lithium does not improve neuromuscular phenotype in a mouse model of severe spinal muscular atrophy.慢性锂治疗不能改善严重脊髓性肌萎缩症小鼠模型的神经肌肉表型。
Neuroscience. 2013 Oct 10;250:417-33. doi: 10.1016/j.neuroscience.2013.07.026. Epub 2013 Jul 19.
10
ERK MAPK signaling pathway inhibition as a potential target to prevent autophagy alterations in Spinal Muscular Atrophy motoneurons.抑制ERK MAPK信号通路作为预防脊髓性肌萎缩运动神经元自噬改变的潜在靶点。
Cell Death Discov. 2023 Apr 5;9(1):113. doi: 10.1038/s41420-023-01409-x.

引用本文的文献

1
Network pharmacology approach to unravel the neuroprotective potential of natural products: a narrative review.基于网络药理学方法解析天然产物的神经保护潜力:一篇综述
Mol Divers. 2025 Apr 25. doi: 10.1007/s11030-025-11198-3.
2
The role of NLRP3 inflammasome in multiple sclerosis: pathogenesis and pharmacological application.NLRP3炎性小体在多发性硬化症中的作用:发病机制及药理学应用。
Front Immunol. 2025 Apr 2;16:1572140. doi: 10.3389/fimmu.2025.1572140. eCollection 2025.
3
[Research progress on phenotypic modifier genes in spinal muscular atrophy].

本文引用的文献

1
Spinal Muscular Atrophy: The Past, Present, and Future of Diagnosis and Treatment.脊髓性肌萎缩症:诊断和治疗的过去、现在和未来。
Int J Mol Sci. 2023 Jul 26;24(15):11939. doi: 10.3390/ijms241511939.
2
Long-term nusinersen treatment across a wide spectrum of spinal muscular atrophy severity: a real-world experience.长期依库珠单抗治疗广泛范围脊髓性肌萎缩症严重度:真实世界经验。
Orphanet J Rare Dis. 2023 Aug 4;18(1):230. doi: 10.1186/s13023-023-02769-4.
3
Gene Therapy for Spinal Muscular Atrophy (SMA): A Review of Current Challenges and Safety Considerations for Onasemnogene Abeparvovec (Zolgensma).
[脊髓性肌萎缩症表型修饰基因的研究进展]
Zhongguo Dang Dai Er Ke Za Zhi. 2025 Feb 15;27(2):229-235. doi: 10.7499/j.issn.1008-8830.2410064.
4
CK and LRRK2 Involvement in Neurodegenerative Diseases.CK 和 LRRK2 参与神经退行性疾病。
Int J Mol Sci. 2024 Oct 30;25(21):11661. doi: 10.3390/ijms252111661.
5
Significance of Programmed Cell Death Pathways in Neurodegenerative Diseases.细胞程序性死亡通路在神经退行性疾病中的意义。
Int J Mol Sci. 2024 Sep 15;25(18):9947. doi: 10.3390/ijms25189947.
6
Real-World Safety Data of the Orphan Drug Onasemnogene Abeparvovec (Zolgensma) for the SMA Rare Disease: A Pharmacovigilance Study Based on the EMA Adverse Event Reporting System.用于脊髓性肌萎缩症罕见病的孤儿药onasemnogene abeparvovec(Zolgensma)的真实世界安全性数据:一项基于欧洲药品管理局不良事件报告系统的药物警戒研究。
Pharmaceuticals (Basel). 2024 Mar 19;17(3):394. doi: 10.3390/ph17030394.
脊髓性肌萎缩症(SMA)的基因治疗:关于onasemnogene abeparvovec(Zolgensma)的当前挑战和安全性考量的综述
Cureus. 2023 Mar 15;15(3):e36197. doi: 10.7759/cureus.36197. eCollection 2023 Mar.
4
Autophagy in Cell Survival and Death.细胞存活和死亡中的自噬作用
Int J Mol Sci. 2023 Mar 1;24(5):4744. doi: 10.3390/ijms24054744.
5
A spinal muscular atrophy modifier implicates the SMN protein in SNARE complex assembly at neuromuscular synapses.脊髓性肌萎缩症修饰物提示 SMN 蛋白参与神经肌肉突触处 SNARE 复合物的组装。
Neuron. 2023 May 3;111(9):1423-1439.e4. doi: 10.1016/j.neuron.2023.02.004. Epub 2023 Mar 1.
6
Dysfunctional mitochondria accumulate in a skeletal muscle knockout model of Smn1, the causal gene of spinal muscular atrophy.在肌萎缩性脊髓侧索硬化症(SMA)的致病基因 Smn1 敲除的骨骼肌模型中,功能失调的线粒体积累。
Cell Death Dis. 2023 Feb 27;14(2):162. doi: 10.1038/s41419-023-05573-x.
7
Autophagy promotes cell survival by maintaining NAD levels.自噬通过维持 NAD 水平促进细胞存活。
Dev Cell. 2022 Nov 21;57(22):2584-2598.e11. doi: 10.1016/j.devcel.2022.10.008.
8
Advances and limitations for the treatment of spinal muscular atrophy.脊髓性肌萎缩症治疗的进展与局限。
BMC Pediatr. 2022 Nov 3;22(1):632. doi: 10.1186/s12887-022-03671-x.
9
Autophagy Dysfunction in ALS: from Transport to Protein Degradation.肌萎缩侧索硬化症中的自噬功能障碍:从运输到蛋白质降解。
J Mol Neurosci. 2022 Jul;72(7):1456-1481. doi: 10.1007/s12031-022-02029-3. Epub 2022 Jun 16.
10
Risdiplam: A Review in Spinal Muscular Atrophy.利司扑兰:治疗脊髓性肌萎缩症的药物。
CNS Drugs. 2022 Apr;36(4):401-410. doi: 10.1007/s40263-022-00910-8. Epub 2022 Mar 13.