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星形胶质细胞对运动神经元损伤的反应通过STAT3调节的TSP-1表达促进结构性突触可塑性。

Astrocyte response to motor neuron injury promotes structural synaptic plasticity via STAT3-regulated TSP-1 expression.

作者信息

Tyzack Giulia E, Sitnikov Sergey, Barson Daniel, Adams-Carr Kerala L, Lau Nike K, Kwok Jessica C, Zhao Chao, Franklin Robin J M, Karadottir Ragnhildur T, Fawcett James W, Lakatos András

机构信息

John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, E.D. Adrian Building, Forvie Site, Robinson Way, Cambridge CB2 0PY, UK.

1] Department of Veterinary Medicine & Wellcome Trust-MRC Stem Cell Institute, University of Cambridge, Madingley Road, Cambridge CB3 0ES, UK [2].

出版信息

Nat Commun. 2014 Jul 11;5:4294. doi: 10.1038/ncomms5294.

DOI:10.1038/ncomms5294
PMID:25014177
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4104454/
Abstract

The role of remote astrocyte (AC) reaction to central or peripheral axonal insult is not clearly understood. Here we use a transgenic approach to compare the direct influence of normal with diminished AC reactivity on neuronal integrity and synapse recovery following extracranial facial nerve transection in mice. Our model allows straightforward interpretations of AC-neuron signalling by reducing confounding effects imposed by inflammatory cells. We show direct evidence that perineuronal reactive ACs play a major role in maintaining neuronal circuitry following distant axotomy. We reveal a novel function of astrocytic signal transducer and activator of transcription-3 (STAT3). STAT3 regulates perineuronal astrocytic process formation and re-expression of a synaptogenic molecule, thrombospondin-1 (TSP-1), apart from supporting neuronal integrity. We demonstrate that, through this new pathway, TSP-1 is responsible for the remote AC-mediated recovery of excitatory synapses onto axotomized motor neurons in adult mice. These data provide new targets for neuroprotective therapies via optimizing AC-driven plasticity.

摘要

远程星形胶质细胞(AC)对中枢或外周轴突损伤的反应作用尚不清楚。在此,我们采用转基因方法,比较正常AC反应性降低与正常AC反应性对小鼠颅外面神经横断后神经元完整性和突触恢复的直接影响。我们的模型通过减少炎症细胞带来的混杂效应,使AC-神经元信号传导的解释更加直接明了。我们提供了直接证据,表明神经元周围的反应性AC在远处轴突切断后维持神经元回路中起主要作用。我们揭示了星形胶质细胞信号转导和转录激活因子3(STAT3)的新功能。除了支持神经元完整性外,STAT3还调节神经元周围星形胶质细胞突起的形成以及突触生成分子血小板反应蛋白-1(TSP-1)的重新表达。我们证明,通过这条新途径,TSP-1负责成年小鼠轴突切断的运动神经元上兴奋性突触的远程AC介导的恢复。这些数据通过优化AC驱动的可塑性为神经保护疗法提供了新的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65d/4104454/38f8d51f284f/ncomms5294-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65d/4104454/23f759e3ceee/ncomms5294-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65d/4104454/90dbd6d02388/ncomms5294-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65d/4104454/d5d395038687/ncomms5294-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65d/4104454/ce8d5e4be63d/ncomms5294-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65d/4104454/38f8d51f284f/ncomms5294-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65d/4104454/23f759e3ceee/ncomms5294-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65d/4104454/29ca1cf89200/ncomms5294-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65d/4104454/f2bdd7008a7f/ncomms5294-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65d/4104454/90dbd6d02388/ncomms5294-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65d/4104454/d5d395038687/ncomms5294-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65d/4104454/ce8d5e4be63d/ncomms5294-f6.jpg
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