Nikandrov V N, Zhuk O N
Morfologiia. 2005;128(5):33-6.
The aim of this study was to determine the effect of streptokinase (SK) on the ultrastructure of cellular elements in the cerebral cortex of newborn rats in vitro. Three series of cell cultures grown on DMEM were used, including those grown on the medium enriched with 15% fetal calf serum (control 1), cultures transferred to the depleted medium containing only 0.5% of this serum (control 2), and the experimental cultures, to which SK (2000 IU/ml) was added. Addition of SK to the medium prevented a reduction of the viability of mature (14 days) dissociated neocortical cell culture from 1-2-day-old rats, induced by a transfer of the culture to a blood serum protein-deficient medium. In a 7-day culture SK potentiated the decrease in the cell viability. In organotypical cultures, with the use of electron microscopy, it was found that SK in concentration used prevented the development of destructive changes in astrocytes, oligodendrocytes, and neurons of explants, induced by a deficit in serum proteins. The neurons contained numerous mitochondria, some of which had only a few cristae. Signs of destruction were observed only in neuronal nuclei. After exposure to SK for 48 hours an activation of oligodendrocytes (containing numerous myelin bodies) was noted which was accompanied by astrocyte disintegration (with hyperchromatic nuclei in the remaining cells). The neurons were resistant to SK exposure.
本研究的目的是在体外确定链激酶(SK)对新生大鼠大脑皮质细胞成分超微结构的影响。使用了在DMEM上培养的三组细胞培养物,包括在富含15%胎牛血清的培养基上生长的培养物(对照1)、转移到仅含0.5%该血清的贫化培养基中的培养物(对照2)以及添加了SK(2000 IU/ml)的实验性培养物。向培养基中添加SK可防止将培养物转移至血清蛋白缺乏的培养基所诱导的1-2日龄大鼠成熟(14天)解离新皮质细胞培养物活力的降低。在7天的培养中,SK增强了细胞活力的下降。在器官型培养物中,通过电子显微镜观察发现,所用浓度的SK可防止血清蛋白缺乏所诱导的外植体星形胶质细胞、少突胶质细胞和神经元发生破坏性变化。神经元含有大量线粒体,其中一些线粒体只有少量嵴。仅在神经元细胞核中观察到破坏迹象。在暴露于SK 48小时后,观察到少突胶质细胞活化(含有大量髓鞘小体),同时伴有星形胶质细胞解体(剩余细胞的细胞核染色质增多)。神经元对SK暴露具有抗性。