Vernadakis A, Davies D, Sakellaridis N, Mangoura D
J Neurosci Res. 1986;15(1):79-85. doi: 10.1002/jnr.490150108.
Glial cell cultures derived from newborn and aged (18-month-old) mouse cerebral hemispheres and maintained up to cell passage 11 were characterized immunocytochemically by using glial fibrillary acidic protein (GFA), and biochemically by using glutamine synthetase (GS), for astrocytes, and 2',3' cyclic nucleotide 3' phosphohydrolase (CNP) for oligodendrocytes. We report here the changes occurring during passages 5-11. GS and CNP activities did not significantly change with cell passage in cultures from newborn mouse. In cultures derived from aged mouse, CNP activity did not change significantly whereas GS activity increased severalfold. A characteristic finding in higher cell passages (passage #7) was the loss of GFA-positive stained cells and the appearance of multinucleated cells. We interpret these changes in culture to represent possible signs of cellular senescence.
从新生和老年(18个月大)小鼠大脑半球获得的神经胶质细胞培养物,维持到第11代细胞传代,通过使用胶质纤维酸性蛋白(GFA)进行免疫细胞化学鉴定,并通过使用谷氨酰胺合成酶(GS)对星形胶质细胞进行生化鉴定,以及使用2',3'环核苷酸3'磷酸水解酶(CNP)对少突胶质细胞进行生化鉴定。我们在此报告第5 - 11代传代过程中发生的变化。在新生小鼠的培养物中,GS和CNP活性不会随着细胞传代而显著变化。在老年小鼠的培养物中,CNP活性没有显著变化,而GS活性增加了几倍。在较高细胞传代(第7代)中的一个特征性发现是GFA阳性染色细胞的丢失和多核细胞的出现。我们将培养物中的这些变化解释为细胞衰老的可能迹象。