Petito C K
J Cereb Blood Flow Metab. 1986 Oct;6(5):616-24. doi: 10.1038/jcbfm.1986.109.
The effects of cerebral ischemia on perineuronal glia were studied in the rat model of transient four-vessel occlusion. Striatum containing irreversibly injured neurons and paramedian cerebral cortex containing reversibly injured neurons were prepared for electron microscopy at intervals of 3 min up to 24 h following ischemia. Perineuronal astrocytes showed cytoplasmic swelling and configurational changes in and pleomorphism of mitochondria similar to those described previously in parenchymal astrocytes in this model. Dark oligodendroglia showed only transient swelling of cisterns of Golgi apparatus and endoplasmic reticulum. However, medium-light oligodendrocytes significantly increased in size and accumulated microtubules and tubovesicular profiles in the cytoplasm. Reactive glia with features of both oligodendrocytes and astrocytes appeared at 15 min. A sharp drop in the number of perineuronal medium-light oligodendrocytes occurred at 3 h after ischemia and was accompanied by increased numbers of astrocytes and intermediate glia. Cortical glia showed similar changes that were milder and reversible. These studies suggest that certain perineuronal glia are transformed into reactive astrocytes in areas of ischemic neuronal necrosis, although current data are insufficient to determine if the transforming cells are astrocytes, light oligodendrocytes, or intermediate glia. Possible stimuli for these glial reactions include loss of or changes in neuronal trophic factors upon CNS glia or alterations in the interstitial fluid composition.
在短暂性四动脉闭塞大鼠模型中研究了脑缺血对神经元周围胶质细胞的影响。在缺血后长达24小时的时间内,每隔3分钟对含有不可逆损伤神经元的纹状体和含有可逆损伤神经元的大脑正中旁皮质进行电子显微镜检查。神经元周围星形胶质细胞表现出细胞质肿胀以及线粒体的形态变化和多形性,类似于该模型中先前在实质星形胶质细胞中所描述的情况。暗型少突胶质细胞仅显示高尔基体和内质网池的短暂肿胀。然而,中亮型少突胶质细胞大小显著增加,细胞质中积累了微管和微管泡结构。具有少突胶质细胞和星形胶质细胞特征的反应性胶质细胞在15分钟时出现。缺血后3小时,神经元周围中亮型少突胶质细胞数量急剧下降,并伴有星形胶质细胞和中间型胶质细胞数量增加。皮质胶质细胞表现出类似的变化,但程度较轻且可逆。这些研究表明,在缺血性神经元坏死区域,某些神经元周围胶质细胞会转化为反应性星形胶质细胞,尽管目前的数据不足以确定转化细胞是星形胶质细胞、轻少突胶质细胞还是中间型胶质细胞。这些胶质细胞反应的可能刺激因素包括中枢神经系统胶质细胞上神经营养因子的丧失或变化,或细胞外液成分的改变。