O'Leary Liam Anuj, Davoli Maria Antonietta, Belliveau Claudia, Tanti Arnaud, Ma Jie Christopher, Farmer William Todd, Turecki Gustavo, Murai Keith Kazuo, Mechawar Naguib
McGill Group for Suicide Studies, Douglas Mental Health University Institute, Verdun, QC, Canada.
Integrated Program in Neuroscience, McGill University, Montreal, QC, Canada.
Front Neuroanat. 2020 Jul 30;14:31. doi: 10.3389/fnana.2020.00031. eCollection 2020.
Astrocytes are commonly identified by their expression of the intermediate filament protein glial fibrillary acidic protein (GFAP). GFAP-immunoreactive (GFAP-IR) astrocytes exhibit regional heterogeneity in density and morphology in the mouse brain as well as morphological diversity in the human cortex. However, regional variations in astrocyte distribution and morphology remain to be assessed comprehensively. This was the overarching objective of this postmortem study, which mainly exploited the immunolabeling of vimentin (VIM), an intermediate filament protein expressed by astrocytes and endothelial cells which presents the advantage of more extensively labeling cell structures. We compared the densities of vimentin-immunoreactive (VIM-IR) and GFAP-IR astrocytes in various brain regions (prefrontal and primary visual cortex, caudate nucleus, mediodorsal thalamus) from male individuals having died suddenly in the absence of neurological or psychiatric conditions. The morphometric properties of VIM-IR in these brain regions were also assessed. We found that VIM-IR astrocytes generally express the canonical astrocytic markers Aldh1L1 and GFAP but that VIM-IR astrocytes are less abundant than GFAP-IR astrocytes in all human brain regions, particularly in the thalamus, where VIM-IR cells were nearly absent. About 20% of all VIM-IR astrocytes presented a twin cell morphology, a phenomenon rarely observed for GFAP-IR astrocytes. Furthermore VIM-IR astrocytes in the striatum were often seen to extend numerous parallel processes which seemed to give rise to large VIM-IR fiber bundles projecting over long distances. Moreover, morphometric analyses revealed that VIM-IR astrocytes were more complex than their mouse counterparts in functionally homologous brain regions, as has been previously reported for GFAP-IR astrocytes. Lastly, the density of GFAP-IR astrocytes in gray and white matter were inversely correlated with vascular density, but for VIM-IR astrocytes this was only the case in gray matter, suggesting that gliovascular interactions may especially influence the regional heterogeneity of GFAP-IR astrocytes. Taken together, these findings reveal special features displayed uniquely by human VIM-IR astrocytes and illustrate that astrocytes display important region- and marker-specific differences in the healthy human brain.
星形胶质细胞通常通过其对中间丝蛋白胶质纤维酸性蛋白(GFAP)的表达来识别。GFAP免疫反应性(GFAP-IR)星形胶质细胞在小鼠大脑中表现出密度和形态的区域异质性,以及在人类皮质中的形态多样性。然而,星形胶质细胞分布和形态的区域差异仍有待全面评估。这是这项尸检研究的总体目标,该研究主要利用波形蛋白(VIM)的免疫标记,波形蛋白是一种由星形胶质细胞和内皮细胞表达的中间丝蛋白,具有更广泛标记细胞结构的优势。我们比较了在无神经或精神疾病情况下突然死亡的男性个体的不同脑区(前额叶和初级视觉皮质、尾状核、丘脑背内侧核)中波形蛋白免疫反应性(VIM-IR)和GFAP-IR星形胶质细胞的密度。还评估了这些脑区中VIM-IR的形态学特性。我们发现,VIM-IR星形胶质细胞通常表达典型的星形胶质细胞标志物醛脱氢酶1家族成员L1(Aldh1L1)和GFAP,但在所有人类脑区中,VIM-IR星形胶质细胞比GFAP-IR星形胶质细胞数量少,尤其是在丘脑中,几乎没有VIM-IR细胞。所有VIM-IR星形胶质细胞中约20%呈现双细胞形态,这一现象在GFAP-IR星形胶质细胞中很少见。此外,经常可以看到纹状体中的VIM-IR星形胶质细胞延伸出许多平行的突起,似乎形成了远距离投射的大的VIM-IR纤维束。此外,形态学分析表明,与功能同源脑区的小鼠星形胶质细胞相比,VIM-IR星形胶质细胞更复杂,正如之前对GFAP-IR星形胶质细胞的报道。最后,GFAP-IR星形胶质细胞在灰质和白质中的密度与血管密度呈负相关,但对于VIM-IR星形胶质细胞,仅在灰质中如此,这表明神经胶质血管相互作用可能尤其影响GFAP-IR星形胶质细胞的区域异质性。综上所述,这些发现揭示了人类VIM-IR星形胶质细胞独特呈现的特殊特征,并表明星形胶质细胞在健康人类大脑中表现出重要的区域和标志物特异性差异。