Kumpulainen T, Dahl D, Korhonen L K, Nyström S H
J Histochem Cytochem. 1983 Jul;31(7):879-86. doi: 10.1177/31.7.6406590.
The specificities of carbonic anhydrase isoenzyme C (CA C) and glial fibrillary acidic (GFA) protein as immunocytochemical markers for different glial cell populations in human brain and retina were studied using indirect immunofluorescence and peroxidase-antiperoxidase complex methods. With antibodies against CA C, only those cerebral cells that were morphologically oligodendrocytes and Müller cells of the retina showed positive immunostaining reaction, whereas antibodies against GFA protein selectively labeled cerebral astrocytes and a part of the glial cells and fibers in the inner layers of the retina. In double labeling, when both glial cell markers were successively localized in the same cerebral tissue sections, GFA protein immunofluorescence was never found in the immunoperoxidase-stained CA C-positive cells, which further supports the oligodendrocyte-specificity of CA C in human brain.
采用间接免疫荧光法和过氧化物酶-抗过氧化物酶复合物法,研究了碳酸酐酶同工酶C(CA C)和胶质纤维酸性蛋白(GFA)作为人脑和视网膜中不同胶质细胞群体免疫细胞化学标志物的特异性。用抗CA C抗体检测时,只有那些形态上为少突胶质细胞和视网膜Müller细胞的脑细胞呈现阳性免疫染色反应,而抗GFA蛋白抗体则选择性地标记了脑星形胶质细胞以及视网膜内层的部分胶质细胞和纤维。在双重标记中,当两种胶质细胞标志物先后定位在同一脑组织切片中时,在免疫过氧化物酶染色的CA C阳性细胞中从未发现GFA蛋白免疫荧光,这进一步支持了CA C在人脑中的少突胶质细胞特异性。