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填补空白——呼吁在区域和损伤特异性背景下对胶质瘢痕的细胞外基质进行全面分析。

Filling the Gaps - A Call for Comprehensive Analysis of Extracellular Matrix of the Glial Scar in Region- and Injury-Specific Contexts.

作者信息

Kjell Jacob, Götz Magdalena

机构信息

Division of Physiological Genomics, Biomedical Center, Ludwig Maximilian University of Munich, Munich, Germany.

Institute for Stem Cell Research, Helmholtz Zentrum München, Munich, Germany.

出版信息

Front Cell Neurosci. 2020 Feb 20;14:32. doi: 10.3389/fncel.2020.00032. eCollection 2020.

DOI:10.3389/fncel.2020.00032
PMID:32153367
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7050652/
Abstract

Central nervous system (CNS) injury results in chronic scar formation that interferes with function and inhibits repair. Extracellular matrix (ECM) is prominent in the scar and potently regulates cell behavior. However, comprehensive information about the ECM proteome is largely lacking, and region- as well as injury-specific differences are often not taken into account. These aspects are the focus of our perspective on injury and scar formation. To highlight the importance of such comprehensive proteome analysis we include data obtained with novel analysis tools of the ECM composition in the scar and show the contribution of monocytes to the ECM composition after traumatic brain injury (TBI). Monocyte invasion was reduced using the CCR2-/- mouse line and step-wise de-cellularization and proteomics allowed determining monocyte-dependent ECM composition and architecture of the glial scar. We find significant reduction in the ECM proteins Tgm1, Itih (1,2, and 3), and Ftl in the absence of monocyte invasion. We also describe the scar ECM comprising zones with distinctive composition and show a subacute signature upon comparison to proteome obtained at earlier times after TBI. These results are discussed in light of injury-, region- and time-specific regulation of scar formation highlighting the urgent need to differentiate injury conditions and CNS-regions using comprehensive ECM analysis.

摘要

中枢神经系统(CNS)损伤会导致慢性瘢痕形成,干扰功能并抑制修复。细胞外基质(ECM)在瘢痕中很突出,并有力地调节细胞行为。然而,关于ECM蛋白质组的全面信息在很大程度上是缺乏的,而且区域以及损伤特异性差异往往未被考虑在内。这些方面是我们对损伤和瘢痕形成观点的重点。为了突出这种全面蛋白质组分析的重要性,我们纳入了用新型分析工具获得的瘢痕中ECM组成的数据,并展示了单核细胞对创伤性脑损伤(TBI)后ECM组成的贡献。使用CCR2-/-小鼠品系减少单核细胞浸润,逐步去细胞化和蛋白质组学能够确定单核细胞依赖性ECM组成和胶质瘢痕的结构。我们发现在没有单核细胞浸润的情况下,ECM蛋白Tgm1、Itih(1、2和3)和Ftl显著减少。我们还描述了瘢痕ECM包含具有独特组成的区域,并与TBI后早期获得的蛋白质组相比显示出亚急性特征。根据损伤、区域和时间特异性的瘢痕形成调节对这些结果进行了讨论,强调了使用全面的ECM分析来区分损伤情况和中枢神经系统区域的迫切需要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c0b/7050652/82174775d5bc/fncel-14-00032-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c0b/7050652/32263cc65963/fncel-14-00032-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c0b/7050652/82174775d5bc/fncel-14-00032-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c0b/7050652/32263cc65963/fncel-14-00032-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c0b/7050652/82174775d5bc/fncel-14-00032-g002.jpg

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