Lossinsky A S, Vorbrodt A W, Wisniewski H M, Iwanowski L
Acta Neuropathol. 1981;53(3):197-202. doi: 10.1007/BF00688022.
An investigation designed to define relationships between endothelial channels and lysosomes was conducted in the mammalian brain microvasculature. Microvessels from normal and mechanically injured mouse brains were studied ultracytochemically for: (1) transport of horseradish peroxidase (HRP) protein tracer through endothelial channels, and (2) for acid phosphatase (AcP) activity as an enzymatic marker of lysosomes. Following traumatic brain injury for 1 week with 2 h circulation of intravenously injected HRP, selected brain slices were processed for ultrastructural localization of either HRP, AcP, or for both reactions together within the same tissue slices. One week after blood-brain barrier (BBB) damage, the presence of HRP reaction product (RP) was observed within endothelial channels and vesicles of capillaries and arterioles with concomitant increase in lysosomal enzymatic activity of the endothelial cells bordering regions of brain damage. Lysosomes were observed to be directly connected to the endothelial channels. Our observations present cytochemical evidence for endothelial channel-lysosome connections which may suggest intralysosomal modification of blood-born materials before entering the neuropil. Such modification could have important immunological and/or metabolic significance.
在哺乳动物脑微血管系统中开展了一项旨在明确内皮通道与溶酶体之间关系的研究。对来自正常和机械损伤小鼠大脑的微血管进行了超微细胞化学研究,内容包括:(1)辣根过氧化物酶(HRP)蛋白示踪剂通过内皮通道的运输,以及(2)酸性磷酸酶(AcP)活性,作为溶酶体的酶标记物。在创伤性脑损伤1周后,静脉注射HRP并循环2小时,对选定的脑切片进行处理,以在同一组织切片内对HRP、AcP或两者反应进行超微结构定位。血脑屏障(BBB)损伤1周后,在毛细血管和小动脉的内皮通道和囊泡内观察到HRP反应产物(RP)的存在,同时在脑损伤区域边界的内皮细胞溶酶体酶活性增加。观察到溶酶体直接与内皮通道相连。我们的观察结果提供了内皮通道-溶酶体连接的细胞化学证据,这可能表明血源性物质在进入神经毡之前在溶酶体内发生了修饰。这种修饰可能具有重要的免疫和/或代谢意义。