Rakic Sonja, Zecevic Nada
Department of Neuroscience, University of Connecticut Medical School, Farmington, Connecticut 06030, USA.
Glia. 2003 Jan 15;41(2):117-27. doi: 10.1002/glia.10140.
Oligodendrocytes, the myelin-producing cells in the central nervous system, represent a large portion of the total number of cells in the human brain. Using cell-specific markers and antibodies to ventral homeodomain transcription factors, NKX2.1 and DLX2, we show here that a subpopulation of early oligodendrocyte progenitor cells (OPCs) in the human telencephalon may originate in the ganglionic eminence (GE). DLX2-labeled OPCs form a well-delineated stream of cells connecting the GE subventricular zone (SVZ) to the cortical intermediate zone through the anterior cortical SVZ. This population of cells is labeled by early OPCs markers, PDGFRalpha, Olig1, and NG2, and not with either neuronal, astrocyte, or late OPCs markers. Intriguingly, numerous CD68(+) microglia/macrophages, nestin(+) neural stem cells, and CD34(+) hematopoietic stem cells (HSCs) are also present in both the GE stream and the cortical SVZ. These cells could be colabeled with DLX2 as well as early OPCs markers. A separate subpopulation of early OPCs, present in the GE and cortical SVZ, did not express either DLX2 or CD68. These findings suggest that different subpopulations of early OPCs, characterized with different sets of transcription factors and cell-specific markers, are present in human forebrain. These subpopulations may have different origins; one may originate in the cortical SVZ, while others may come from the GE and/or outside the CNS as hematopoietic stem cells.
少突胶质细胞是中枢神经系统中产生髓磷脂的细胞,在人类大脑的细胞总数中占很大比例。利用细胞特异性标志物以及针对腹侧同源结构域转录因子NKX2.1和DLX2的抗体,我们在此表明,人类端脑中早期少突胶质前体细胞(OPC)的一个亚群可能起源于神经节隆起(GE)。DLX2标记的OPC形成了一条界限清晰的细胞流,通过前皮质室管膜下区(SVZ)将GE室管膜下区与皮质中间区连接起来。这群细胞被早期OPC标志物PDGFRα、Olig1和NG2标记,而不被神经元、星形胶质细胞或晚期OPC标志物标记。有趣的是,在GE细胞流和皮质SVZ中也存在大量CD68(+)小胶质细胞/巨噬细胞、巢蛋白(+)神经干细胞和CD34(+)造血干细胞(HSC)。这些细胞可以与DLX2以及早期OPC标志物共同标记。存在于GE和皮质SVZ中的另一群早期OPC不表达DLX2或CD68。这些发现表明,人类前脑中存在不同亚群的早期OPC,它们以不同的转录因子和细胞特异性标志物为特征。这些亚群可能有不同的起源;一个可能起源于皮质SVZ,而其他的可能来自GE和/或作为造血干细胞来自中枢神经系统之外。