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

胶质增生 病变 小胶质细胞 白质 大脑皮层 生物 病理 星形胶质细胞 神经科学 神经胶质 皮质(解剖学) 胶质瘢痕 炎症 中枢神经系统 医学 免疫学 磁共振成像 放射科
作者
Nicola Mattugini,Juliane Merl‐Pham,Elisabetta Petrozziello,Lisa Schindler,Jürgen Bernhagen,Stefanie M. Hauck,Magdalena Götz
出处
期刊:Glia [Wiley]
卷期号:66 (8): 1644-1662 被引量:28
标识
DOI:10.1002/glia.23329
摘要

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.

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