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Rac-曼尼诺夫和 Rho-罗索夫:兴奋性突触中 Rho-GTP 酶信号的交响乐。

Rac-maninoff and Rho-vel: The symphony of Rho-GTPase signaling at excitatory synapses.

机构信息

Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA.

Integrative Molecular and Biomedical Science Graduate Program, Baylor College of Medicine, Houston, TX, USA.

出版信息

Small GTPases. 2022 Jan;13(1):14-47. doi: 10.1080/21541248.2021.1885264. Epub 2021 May 6.

DOI:10.1080/21541248.2021.1885264
PMID:33955328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9707551/
Abstract

Synaptic connections between neurons are essential for every facet of human cognition and are thus regulated with extreme precision. Rho-family GTPases, molecular switches that cycle between an active GTP-bound state and an inactive GDP-bound state, comprise a critical feature of synaptic regulation. Rho-GTPases are exquisitely controlled by an extensive suite of activators (GEFs) and inhibitors (GAPs and GDIs) and interact with many different signalling pathways to fulfill their roles in orchestrating the development, maintenance, and plasticity of excitatory synapses of the central nervous system. Among the mechanisms that control Rho-GTPase activity and signalling are cell surface receptors, GEF/GAP complexes that tightly regulate single Rho-GTPase dynamics, GEF/GAP and GEF/GEF functional complexes that coordinate multiple Rho-family GTPase activities, effector positive feedback loops, and mutual antagonism of opposing Rho-GTPase pathways. These complex regulatory mechanisms are employed by the cells of the nervous system in almost every step of development, and prominently figure into the processes of synaptic plasticity that underlie learning and memory. Finally, misregulation of Rho-GTPases plays critical roles in responses to neuronal injury, such as traumatic brain injury and neuropathic pain, and in neurodevelopmental and neurodegenerative disorders, including intellectual disability, autism spectrum disorder, schizophrenia, and Alzheimer's Disease. Thus, decoding the mechanisms of Rho-GTPase regulation and function at excitatory synapses has great potential for combatting many of the biggest current challenges in mental health.

摘要

神经元之间的突触连接对于人类认知的各个方面都是必不可少的,因此它们受到了极其精确的调控。Rho 家族 GTPases 是分子开关,能够在活性 GTP 结合状态和非活性 GDP 结合状态之间循环,是突触调节的关键特征。Rho-GTPases 受到广泛的激活剂(GEFs)和抑制剂(GAPs 和 GDIs)的精细调控,并与许多不同的信号通路相互作用,以发挥其在协调中枢神经系统兴奋性突触的发育、维持和可塑性中的作用。控制 Rho-GTPase 活性和信号转导的机制包括细胞表面受体、紧密调节单个 Rho-GTPase 动力学的 GEF/GAP 复合物、协调多个 Rho 家族 GTPase 活性的 GEF/GAP 和 GEF/GEF 功能复合物、效应物正反馈回路以及相互拮抗的 Rho-GTPase 通路。这些复杂的调节机制被神经系统中的细胞用于发育的几乎每一个步骤,并突出体现在学习和记忆所依赖的突触可塑性过程中。最后,Rho-GTPases 的失调在神经元损伤的反应中起着关键作用,例如创伤性脑损伤和神经性疼痛,以及神经发育和神经退行性疾病,包括智力障碍、自闭症谱系障碍、精神分裂症和阿尔茨海默病。因此,解码 Rho-GTPase 在兴奋性突触中的调节和功能机制,对于应对当前心理健康领域的最大挑战具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/3ed37ed04575/KSGT_A_1885264_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/52f782f1799c/KSGT_A_1885264_F0001_OC.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/198b4f8ff7f5/KSGT_A_1885264_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/19ca0988b466/KSGT_A_1885264_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/279e63f6bf05/KSGT_A_1885264_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/3ed37ed04575/KSGT_A_1885264_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/52f782f1799c/KSGT_A_1885264_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/df471a5535e9/KSGT_A_1885264_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/3f6c497a56ee/KSGT_A_1885264_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/198b4f8ff7f5/KSGT_A_1885264_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/19ca0988b466/KSGT_A_1885264_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/279e63f6bf05/KSGT_A_1885264_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d056/9707551/3ed37ed04575/KSGT_A_1885264_F0007_OC.jpg

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