大脑中细胞粘附和自噬的合作:在发育和神经退行性疾病中的功能作用。

Q1 Medicine
Sarah J. Hernandez , Gianna Fote , Andrea M. Reyes-Ortiz , Joan S. Steffan , Leslie M. Thompson
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引用次数: 7

摘要

细胞外基质(ECM)引导的细胞粘附连接和自噬维持细胞稳态似乎是不同的功能,它们在分子上相互交织,相互调节。这是大脑中一个新兴的领域,粘附和自噬之间的相互作用在神经保护和神经退行性变的交叉点发挥作用。ECM和粘附蛋白调节自噬反应以直接清除蛋白质,并指导大脑疾病中出现问题的再生程序。同时,自噬流量调节粘附动力学,介导神经突生长和突触可塑性,并伴有神经退行性疾病引起的功能破坏。这篇综述强调了在健康和疾病期间,大脑中细胞粘附和自噬之间的合作交换。由于粘附和自噬之间的机制联盟已被用于治疗转移性疾病,了解指导粘附和自吞噬之间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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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

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.

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来源期刊
Matrix Biology Plus
Matrix Biology Plus Medicine-Histology
CiteScore
9.00
自引率
0.00%
发文量
25
审稿时长
105 days
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