Bushong Eric A, Martone Maryann E, Jones Ying Z, Ellisman Mark H
National Center for Microscopy and Imaging Research, University of California, San Diego, La Jolla, California 92093-0608, USA.
J Neurosci. 2002 Jan 1;22(1):183-92. doi: 10.1523/JNEUROSCI.22-01-00183.2002.
Protoplasmic astrocytes are increasingly thought to interact extensively with neuronal elements in the brain and to influence their activity. Recent reports have also begun to suggest that physiologically, and perhaps functionally, diverse forms of these cells may be present in the CNS. Our current understanding of astrocyte form and distribution is based predominantly on studies that used the astrocytic marker glial fibrillary acidic protein (GFAP) and on studies using metal-impregnation techniques. The prevalent opinion, based on studies using these methods, is that astrocytic processes overlap extensively and primarily share the underlying neuropil. However, both of these techniques have serious shortcomings for visualizing the interactions among these structurally complex cells. In the present study, intracellular injection combined with immunohistochemistry for GFAP show that GFAP delineates only approximately 15% of the total volume of the astrocyte. As a result, GFAP-based images have led to incorrect conclusions regarding the interaction of processes of neighboring astrocytes. To investigate these interactions in detail, groups of adjacent protoplasmic astrocytes in the CA1 stratum radiatum were injected with fluorescent intracellular tracers of distinctive emissive wavelengths and analyzed using three-dimensional (3D) confocal analysis and electron microscopy. Our findings show that protoplasmic astrocytes establish primarily exclusive territories. The knowledge of how the complex morphology of protoplasmic astrocytes affects their 3D relationships with other astrocytes, oligodendroglia, neurons, and vasculature of the brain should have important implications for our understanding of nervous system function.
人们越来越认为,原生质型星形胶质细胞与大脑中的神经元成分广泛相互作用并影响其活动。最近的报告也开始表明,在中枢神经系统中可能存在生理上乃至功能上不同形式的这些细胞。我们目前对星形胶质细胞形态和分布的理解主要基于使用星形胶质细胞标志物胶质纤维酸性蛋白(GFAP)的研究以及使用金属浸染技术的研究。基于使用这些方法的研究,普遍的观点是星形胶质细胞的突起广泛重叠,并且主要共享潜在的神经毡。然而,这两种技术在可视化这些结构复杂的细胞之间的相互作用方面都存在严重缺陷。在本研究中,细胞内注射结合GFAP免疫组织化学表明,GFAP仅勾勒出星形胶质细胞总体积的约15%。因此,基于GFAP的图像导致了关于相邻星形胶质细胞突起相互作用的错误结论。为了详细研究这些相互作用,向CA1辐射层中的相邻原生质型星形胶质细胞群注射具有独特发射波长的荧光细胞内示踪剂,并使用三维(3D)共聚焦分析和电子显微镜进行分析。我们的研究结果表明,原生质型星形胶质细胞主要建立排他性区域。了解原生质型星形胶质细胞的复杂形态如何影响其与其他星形胶质细胞、少突胶质细胞、神经元和脑血管系统的三维关系,对于我们理解神经系统功能应该具有重要意义。