Kirik O V, Sukhorukova E G, Korzhevskiĭ D E
Morfologiia. 2010;137(2):5-8.
At present, calcium-binding Iba-1 protein is considered to be identical to AIF-1 protein and it is used as one of the selective microglia markers. However, the data on the cell populations capable of expressing Iba-1/AIF-1, are inconsistent. The aims of the present study were to identify rat brain cells expressing Iba-1 and to define their structural characteristics. The methods of immunocytochemistry and confocal laser microscopy were used. Iba-1 protein was detected only in microglial cells, macrophages of brain meninges, supraependymal macrophages, superficial and stromal cells of the choroid plexus--all the cells possessing phagocytotic function. Comparison of the data obtained with the results of other studies allows to suggest that not all of commonly used antibodies against Iba-1/AIF-1 demonstrate the same product. It can not be excluded, that it can be associated with the presence of alternative splicing of Iba-1 mRNA.
目前,钙结合蛋白Iba-1被认为与AIF-1蛋白相同,并被用作选择性小胶质细胞标志物之一。然而,关于能够表达Iba-1/AIF-1的细胞群体的数据并不一致。本研究的目的是鉴定大鼠脑内表达Iba-1的细胞,并确定其结构特征。采用了免疫细胞化学和共聚焦激光显微镜方法。Iba-1蛋白仅在小胶质细胞、脑膜巨噬细胞、室管膜上巨噬细胞、脉络丛的表层和基质细胞中检测到,所有这些细胞都具有吞噬功能。将所得数据与其他研究结果进行比较表明,并非所有常用的抗Iba-1/AIF-1抗体都能识别相同的产物。不能排除这可能与Iba-1 mRNA的可变剪接有关。