Skoff R P, Ghandour M S, Knapp P E
Department of Anatomy and Cell Biology, Wayne State University School of Medicine, Detroit, Michigan 48201.
Glia. 1994 Sep;12(1):12-23. doi: 10.1002/glia.440120103.
The phenotype of proliferating glia is examined during postnatal rodent development by combining immunocytochemistry (ICC) with 3H-thymidine autoradiography (ARG) to identify cells in the S phase of the cell cycle. Antibodies (ABs) which are specific for cells in the oligodendrocyte (OL) lineage were utilized, with emphasis placed upon the proliferation of OLs as it remains unclear whether this cell type divides in situ. The results show that proliferating cells stain with ABs which are specific for OLs and myelin glycolipids. The proliferating OLs (oligodendroblasts), although they do not appear to have formed myelin sheaths, have quite elaborate and distinctive morphologies. These oligodendroblasts give rise to very long, thin processes which in turn have additional branches. Their cytoarchitecture corresponds closely to cells described as oligodendroblasts with electron microscopy and whose processes often appear to be in the initial phase of myelination (Skoff et al: J. Comp. Neurol. 169:291-312, 1976a). These proliferating OLs are still quite immature because the expression of myelin specific proteins is only occasionally observed in 3H-thymidine labeled cells. The phenotype of the oligodendroblasts is quite different from that of proliferating astrocytes (astroblasts). As shown in previous studies (Skoff; Dev. Biol. 139:149-163, 1990), the astroblasts, which are identified by the presence of glial fibrillary acidic protein (GFAP), usually have thick, stubby processes, and both their nucleus and cytoplasm are larger and of lighter density than those found in oligodendroblasts. In early myelinating regions of the cerebrum, glycolipid positive cells account for the majority of the 3H-thymidine labeled cells. This data, when combined with the quantification of proliferating astrocytes (ASs) from previous immunocytochemical and electron microscopic studies, indicate that oligodendroblasts and astroblasts constitute the vast majority of the proliferating glia in the brain and in optic nerve at times when ASs and OLs are being generated. In normal postnatal cerebral development, the immature ASs and OLs which proliferate are the direct, immediate precursors for most postmitotic ASs and OLs.
通过将免疫细胞化学(ICC)与³H-胸腺嘧啶放射自显影术(ARG)相结合,以识别处于细胞周期S期的细胞,从而在出生后啮齿动物发育过程中检查增殖神经胶质细胞的表型。使用了对少突胶质细胞(OL)谱系中的细胞具有特异性的抗体(ABs),重点关注OL的增殖情况,因为目前尚不清楚这种细胞类型是否在原位分裂。结果表明,增殖细胞能用对OL和髓磷脂糖脂具有特异性的ABs进行染色。增殖的OL(少突胶质前体细胞)虽然似乎尚未形成髓鞘,但其形态相当精细且独特。这些少突胶质前体细胞会产生非常长且细的突起,这些突起又会有额外的分支。它们的细胞结构与通过电子显微镜描述的少突胶质前体细胞密切对应,其突起通常似乎处于髓鞘形成的初始阶段(斯科夫等人:《比较神经学杂志》169:291 - 312,1976a)。这些增殖的OL仍然相当不成熟,因为在³H-胸腺嘧啶标记的细胞中仅偶尔观察到髓鞘特异性蛋白的表达。少突胶质前体细胞的表型与增殖的星形胶质细胞(星形胶质前体细胞)有很大不同。如先前研究(斯科夫;《发育生物学》139:149 - 163,1990)所示,通过胶质纤维酸性蛋白(GFAP)的存在来识别的星形胶质前体细胞通常具有粗短的突起,并且它们的细胞核和细胞质都比少突胶质前体细胞中的更大且密度更浅。在大脑早期髓鞘形成区域,糖脂阳性细胞占³H-胸腺嘧啶标记细胞的大多数。该数据与先前免疫细胞化学和电子显微镜研究中增殖星形胶质细胞(ASs)的定量结果相结合,表明在ASs和OLs产生时,少突胶质前体细胞和星形胶质前体细胞构成了大脑和视神经中增殖神经胶质细胞的绝大多数。在正常的出生后大脑发育过程中,增殖的未成熟ASs和OLs是大多数有丝分裂后ASs和OLs的直接、即时前体。