人大脑皮质水肿神经细胞溶酶体异常及脂褐素含量。

O J Castejón
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引用次数: 0

摘要

本文对32例先天性脑积水、复杂颅脑外伤、脑肿瘤及血管异常患者缺氧缺血性脑实质中神经细胞、毛细血管内皮细胞和周细胞溶酶体的改变及脂褐素含量进行了检测。对额叶、顶叶和颞叶皮层活检进行透射电镜检查。在水肿的非锥体和锥体神经细胞中,溶酶体显示其限制膜的断裂和相关的致密肉芽。溶酶体周围可见胞浆局灶性坏死。在新生儿和婴儿先天性脑积水患者中也观察到脂褐素颗粒,表明脂褐素的形成是一个生命周期的过程。在年轻和成年脑外伤、肿瘤和血管异常患者中观察到溶酶体与脂褐素颗粒量增加共存。吞噬星形胶质细胞和激活的少突胶质细胞显示了内体/溶酶体系统改变的整体频谱。内皮细胞和周细胞中也可见脂褐素颗粒和多泡体。本文讨论了释放和激活的溶酶体酶在神经细胞胞浆局灶性坏死和中重度水肿发生中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lysosome abnormalities and lipofucsin content of nerve cells of oedematous human cerebral cortex.

Lysosome alterations and lipofucsin content of nerve cells, capillary endothelial cells and pericytes were examined in the anoxic-ischaemic brain parenchyma of thirty two patients with congenital hydrocephalus, complicated brain traumatic injuries, brain tumours and vascular anomalies. Cortical biopsies of frontal, parietal and temporal cortex were processed for transmission electron microscopy. In oedematous non pyramidal and pyramidal nerve cells, lysosomes showed fragmentation of their limiting membranes and an associated dense granulation. Areas of cytoplasmic focal necrosis were observed surrounding the lysosomes. Lipofucsin granules were also observed in neonate and infant patients with congenital hydrocephalus, suggesting that lipofucsin formation is a life span process. Lysosomes coexisting with an increased amount of lipofucsin granules were observed in young and adult patients with brain trauma, tumours and vascular anomalies. Phagocytic astrocytes and activated oligodendroglial cells showed the overall spectrum of an altered endosomal/lysosomal system. Lipofucsin granules and multivesicular bodies also were distinguished in endothelial and pericyte cells. The role of released and activated lysosomal enzymes is discussed in relation with the cytoplasmatic focal necrosis of nerve cells and the genesis of moderate and severe oedema.

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