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Tks5 调节神经肌肉接点处的突触足突形成和突触后机械装置的稳定。

Tks5 Regulates Synaptic Podosome Formation and Stabilization of the Postsynaptic Machinery at the Neuromuscular Junction.

机构信息

Laboratory of Synaptogenesis, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-787 Warszawa, Poland.

Laboratory of Molecular Basis of Cell Motility, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-787 Warszawa, Poland.

出版信息

Int J Mol Sci. 2021 Nov 7;22(21):12051. doi: 10.3390/ijms222112051.

DOI:10.3390/ijms222112051
PMID:34769479
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8585010/
Abstract

Currently, the etiology of many neuromuscular disorders remains unknown. Many of them are characterized by aberrations in the maturation of the neuromuscular junction (NMJ) postsynaptic machinery. Unfortunately, the molecular factors involved in this process are still largely unknown, which poses a great challenge for identifying potential therapeutic targets. Here, we identified Tks5 as a novel interactor of αdystrobrevin-1, which is a crucial component of the NMJ postsynaptic machinery. Tks5 has been previously shown in cancer cells to be an important regulator of actin-rich structures known as invadosomes. However, a role of this scaffold protein at a synapse has never been studied. We show that Tks5 is crucial for remodeling of the NMJ postsynaptic machinery by regulating the organization of structures similar to the invadosomes, known as synaptic podosomes. Additionally, it is involved in the maintenance of the integrity of acetylcholine receptor (AChR) clusters and regulation of their turnover. Lastly, our data indicate that these Tks5 functions may be mediated by its involvement in recruitment of actin filaments to the postsynaptic machinery. Collectively, we show for the first time that the Tks5 protein is involved in regulation of the postsynaptic machinery.

摘要

目前,许多神经肌肉疾病的病因仍然未知。其中许多疾病的特征是神经肌肉接头(NMJ)突触后机制的成熟异常。不幸的是,这一过程中涉及的分子因素在很大程度上仍然未知,这给确定潜在的治疗靶点带来了巨大挑战。在这里,我们鉴定 Tks5 是 αdystrobrevin-1 的一种新型相互作用蛋白,αdystrobrevin-1 是 NMJ 突触后机制的关键组成部分。Tks5 先前已在癌细胞中被证明是一种称为入侵小体的富含肌动蛋白的结构的重要调节剂。然而,这种支架蛋白在突触中的作用从未被研究过。我们表明,Tks5 通过调节类似于入侵小体的结构的组织,对于 NMJ 突触后机制的重塑是至关重要的,这些结构被称为突触足状伪足。此外,它还参与乙酰胆碱受体 (AChR) 簇的完整性的维持和它们的周转率的调节。最后,我们的数据表明,这些 Tks5 功能可能是通过其参与将肌动蛋白丝募集到突触后机制中来介导的。总的来说,我们首次表明 Tks5 蛋白参与调节突触后机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ac/8585010/4c9f9a4b5951/ijms-22-12051-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ac/8585010/d726e585dc8f/ijms-22-12051-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ac/8585010/d7b3aac5455c/ijms-22-12051-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ac/8585010/3e3f0877a75a/ijms-22-12051-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ac/8585010/4c9f9a4b5951/ijms-22-12051-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ac/8585010/d726e585dc8f/ijms-22-12051-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ac/8585010/d7b3aac5455c/ijms-22-12051-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ac/8585010/3e3f0877a75a/ijms-22-12051-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ac/8585010/4c9f9a4b5951/ijms-22-12051-g004.jpg

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Int J Mol Sci. 2020 Oct 30;21(21):8117. doi: 10.3390/ijms21218117.
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The podosome cap: past, present, perspective.足突帽:过去、现在和展望。
Eur J Cell Biol. 2020 Jun;99(5):151087. doi: 10.1016/j.ejcb.2020.151087. Epub 2020 May 25.
3
Arhgef5 Binds α-Dystrobrevin 1 and Regulates Neuromuscular Junction Integrity.
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Front Mol Neurosci. 2020 Jun 10;13:104. doi: 10.3389/fnmol.2020.00104. eCollection 2020.
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The role of the dystrophin glycoprotein complex on the neuromuscular system.营养不良素糖蛋白复合物在神经肌肉系统中的作用。
Neurosci Lett. 2020 Mar 23;722:134833. doi: 10.1016/j.neulet.2020.134833. Epub 2020 Feb 10.
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