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脑白质损伤对成年小鼠大脑皮质刺伤后灰质反应性胶质增生的影响。

Influence of white matter injury on gray matter reactive gliosis upon stab wound in the adult murine cerebral cortex.

机构信息

Physiological Genomics, Biomedical center (BMC), Ludwig-Maximilians-University (LMU), Großhaderner Str. 9, Planegg/Martinsried, 82152, Germany.

Institute of Stem Cell Research, Helmholtz Center Munich, Biomedical Center (BMC), Department of Physiological Genomics, Ludwig-Maximilians-University (LMU), Großhaderner Str. 9, Planegg/Martinsried, 82152, Germany.

出版信息

Glia. 2018 Aug;66(8):1644-1662. doi: 10.1002/glia.23329. Epub 2018 Mar 24.

DOI:10.1002/glia.23329
PMID:29573353
Abstract

Traumatic brain injury frequently affects the cerebral cortex, yet little is known about the differential effects that occur if only the gray matter (GM) is damaged or if the injury also involves the white matter (WM). To tackle this important question and directly compare similarities and differences in reactive gliosis, we performed stab wound injury affecting GM and WM (GM+) and one restricted to the GM (GM-) in the adult murine cerebral cortex. First, we examined glial reactivity in the regions affected (WM and GM) and determined the influence of WM injury on reactive gliosis in the GM comparing the same area in the two injury paradigms. In the GM+ injury microglia proliferation is increased in the WM compared with GM, while proliferating astrocytes are more abundant in the GM than in the WM. Interestingly, WM lesion exerted a strong influence on the proliferation of the GM glial cells that was most pronounced at early stages, 3 days post lesion. While astrocyte proliferation was increased, NG2 glia proliferation was decreased in the GM+ compared with GM- lesion condition. Importantly, these differences were not observed when a lesion of the same size affected only the GM. Unbiased proteomic analyses further corroborate our findings in support of a profound difference in GM reactivity when WM is also injured and revealed MIF as a key regulator of NG2 glia proliferation.

摘要

创伤性脑损伤常影响大脑皮层,但如果仅损伤灰质(GM)或损伤还涉及白质(WM),则发生的差异影响知之甚少。为了解决这个重要问题并直接比较反应性神经胶质增生的相似性和差异性,我们在成年鼠大脑皮层中进行了影响 GM 和 WM(GM+)的刺伤损伤和仅局限于 GM(GM-)的损伤。首先,我们在受影响区域(WM 和 GM)检查了神经胶质反应,并通过比较两种损伤模型中的同一区域,确定 WM 损伤对 GM 中反应性神经胶质增生的影响。在 GM+损伤中,与 GM 相比,WM 中的小胶质细胞增殖增加,而 GM 中增殖的星形胶质细胞比 WM 中更丰富。有趣的是,WM 病变对 GM 神经胶质细胞的增殖有强烈的影响,在病变后 3 天最为明显。星形胶质细胞增殖增加,而 NG2 胶质细胞增殖在 GM+损伤中比 GM-损伤条件下减少。重要的是,当同样大小的病变仅影响 GM 时,没有观察到这些差异。无偏蛋白组学分析进一步证实了我们的发现,支持了当 WM 也受伤时 GM 反应性存在明显差异,并揭示了 MIF 作为 NG2 胶质细胞增殖的关键调节因子。

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