Dzwonek Karolina
Laboratory of Mechanisms of Neurodegeneration and Neuroprotection, Department of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, 3 Pasteur St., 02-093 Warsaw, Poland.
Acta Neurobiol Exp (Wars). 2005;65(2):173-6.
It has been recently proposed that NG2 proteoglycan expressing cells may stand for a unique class of glia in adult CNS referred to as oligodendrocyte progenitor cells (OPCs). These NG2 positive cells can give rise to mature oligodendrocytes, however a large number of them persists in immature stage throughout a lifetime and responds to various types of injury. In order to investigate OPCs reactivity in vitro, a model of trimethyltin evoked neurodegeneration was used. The results demonstrate that NG2 expressing cells survive treatment with the neurotoxin in a concentration that injures most of neurons in the culture. Moreover, progenitors change their morphology when treated with trimethyltin, upregulate the NG2 proteoglycan expression and retain the ability to divide.
最近有人提出,表达NG2蛋白聚糖的细胞可能代表成年中枢神经系统中一类独特的神经胶质细胞,称为少突胶质前体细胞(OPCs)。这些NG2阳性细胞可分化为成熟的少突胶质细胞,然而其中大量细胞在整个生命周期中都处于未成熟阶段,并对各种类型的损伤作出反应。为了研究体外少突胶质前体细胞的反应性,使用了三甲基锡诱发神经退行性变的模型。结果表明,表达NG2的细胞在用神经毒素处理后能够存活,该神经毒素的浓度会损伤培养物中的大多数神经元。此外,前体细胞在用三甲基锡处理后会改变其形态,上调NG2蛋白聚糖的表达,并保留分裂能力。