Suppr超能文献

大脑中细胞黏附与自噬的协同作用:在发育和神经退行性疾病中的功能作用

Cooperation of cell adhesion and autophagy in the brain: Functional roles in development and neurodegenerative disease.

作者信息

Hernandez Sarah J, Fote Gianna, Reyes-Ortiz Andrea M, Steffan Joan S, Thompson Leslie M

机构信息

Neurobiology and Behavior, University of California Irvine, Irvine, CA 92697, USA.

Sue and Bill Gross Stem Cell Research Center, University of California Irvine, Irvine, CA 92697, USA.

出版信息

Matrix Biol Plus. 2021 Oct 23;12:100089. doi: 10.1016/j.mbplus.2021.100089. eCollection 2021 Dec.

Abstract

Cellular adhesive connections directed by the extracellular matrix (ECM) and maintenance of cellular homeostasis by autophagy are seemingly disparate functions that are molecularly intertwined, each regulating the other. This is an emerging field in the brain where the interplay between adhesion and autophagy functions at the intersection of neuroprotection and neurodegeneration. The ECM and adhesion proteins regulate autophagic responses to direct protein clearance and guide regenerative programs that go awry in brain disorders. Concomitantly, autophagic flux acts to regulate adhesion dynamics to mediate neurite outgrowth and synaptic plasticity with functional disruption contributed by neurodegenerative disease. This review highlights the cooperative exchange between cellular adhesion and autophagy in the brain during health and disease. As the mechanistic alliance between adhesion and autophagy has been leveraged therapeutically for metastatic disease, understanding overlapping molecular functions that direct the interplay between adhesion and autophagy might uncover therapeutic strategies to correct or compensate for neurodegeneration.

摘要

由细胞外基质(ECM)引导的细胞黏附连接以及通过自噬维持细胞内稳态,这两种功能看似不同,但在分子层面相互交织,彼此相互调节。这是大脑中一个新兴的领域,其中黏附与自噬功能之间的相互作用发生在神经保护和神经退行性变的交叉点。ECM和黏附蛋白调节自噬反应以直接清除蛋白质,并指导在脑部疾病中出错的再生程序。与此同时,自噬流作用于调节黏附动力学,以介导神经突生长和突触可塑性,而神经退行性疾病会导致功能破坏。本综述强调了健康和疾病状态下大脑中细胞黏附与自噬之间的协同作用。由于黏附与自噬之间的机制联盟已被用于转移性疾病的治疗,了解指导黏附与自噬相互作用的重叠分子功能可能会揭示纠正或补偿神经退行性变的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98c3/8579148/f3cfd14b5047/gr1.jpg

相似文献

1
Cooperation of cell adhesion and autophagy in the brain: Functional roles in development and neurodegenerative disease.
Matrix Biol Plus. 2021 Oct 23;12:100089. doi: 10.1016/j.mbplus.2021.100089. eCollection 2021 Dec.
2
Autophagic flux control in neurodegeneration: Progress and precision targeting-Where do we stand?
Prog Neurobiol. 2017 Jun;153:64-85. doi: 10.1016/j.pneurobio.2017.03.006. Epub 2017 Apr 3.
3
Dysfunctional Autophagy and Endolysosomal System in Neurodegenerative Diseases: Relevance and Therapeutic Options.
Front Cell Neurosci. 2020 Dec 17;14:602116. doi: 10.3389/fncel.2020.602116. eCollection 2020.
4
Autophagic clearance of aggregate-prone proteins associated with neurodegeneration.
Methods Enzymol. 2009;453:83-110. doi: 10.1016/S0076-6879(08)04005-6.
6
Autophagy: Instructions from the extracellular matrix.
Matrix Biol. 2021 Jun;100-101:1-8. doi: 10.1016/j.matbio.2021.06.002. Epub 2021 Jul 2.
9
Novel prospects in targeting neurodegenerative disorders via autophagy.
Eur J Pharmacol. 2024 Dec 5;984:177060. doi: 10.1016/j.ejphar.2024.177060. Epub 2024 Oct 18.
10
Autophagic and endo-lysosomal dysfunction in neurodegenerative disease.
Mol Brain. 2019 Nov 29;12(1):100. doi: 10.1186/s13041-019-0504-x.

引用本文的文献

1
Postmortem Interval Leads to Loss of Disease-Specific Signatures in Brain Tissue.
eNeuro. 2025 Mar 14;12(3). doi: 10.1523/ENEURO.0505-24.2025. Print 2025 Mar.
2
Integrin and Its Associated Proteins as a Mediator for Mechano-Signal Transduction.
Biomolecules. 2025 Jan 23;15(2):166. doi: 10.3390/biom15020166.
4
HiPSC-derived 3D neural models reveal neurodevelopmental pathomechanisms of the Cockayne Syndrome B.
Cell Mol Life Sci. 2024 Aug 23;81(1):368. doi: 10.1007/s00018-024-05406-w.
6
Autophagic-Related Proteins in Brain Gliomas: Role, Mechanisms, and Targeting Agents.
Cancers (Basel). 2023 May 5;15(9):2622. doi: 10.3390/cancers15092622.
7
Single-nuclei transcriptome analysis of Huntington disease iPSC and mouse astrocytes implicates maturation and functional deficits.
iScience. 2022 Dec 6;26(1):105732. doi: 10.1016/j.isci.2022.105732. eCollection 2023 Jan 20.
9
How the mechanical microenvironment of stem cell growth affects their differentiation: a review.
Stem Cell Res Ther. 2022 Aug 13;13(1):415. doi: 10.1186/s13287-022-03070-0.
10
Extracellular matrix guidance of autophagy: a mechanism regulating cancer growth.
Open Biol. 2022 Jan;12(1):210304. doi: 10.1098/rsob.210304. Epub 2022 Jan 5.

本文引用的文献

1
Autophagy: Instructions from the extracellular matrix.
Matrix Biol. 2021 Jun;100-101:1-8. doi: 10.1016/j.matbio.2021.06.002. Epub 2021 Jul 2.
2
The essential role of primary cilia in cerebral cortical development and disorders.
Curr Top Dev Biol. 2021;142:99-146. doi: 10.1016/bs.ctdb.2020.11.003. Epub 2021 Jan 25.
3
The Multifaceted Roles of Primary Cilia in the Development of the Cerebral Cortex.
Front Cell Dev Biol. 2021 Feb 2;9:630161. doi: 10.3389/fcell.2021.630161. eCollection 2021.
5
Filamentous recombinant human Tau activates primary astrocytes via an integrin receptor complex.
Nat Commun. 2021 Jan 4;12(1):95. doi: 10.1038/s41467-020-20322-w.
6
Receptor-mediated clustering of FIP200 bypasses the role of LC3 lipidation in autophagy.
EMBO J. 2020 Dec 15;39(24):e104948. doi: 10.15252/embj.2020104948. Epub 2020 Nov 23.
8
ABHD4-dependent developmental anoikis safeguards the embryonic brain.
Nat Commun. 2020 Aug 31;11(1):4363. doi: 10.1038/s41467-020-18175-4.
9
Huntington's disease alters human neurodevelopment.
Science. 2020 Aug 14;369(6505):787-793. doi: 10.1126/science.aax3338. Epub 2020 Jul 16.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验