Hurley J V, Anderson R M, Sexton P T
J Pathol. 1981 May;134(1):57-70. doi: 10.1002/path.1711340107.
Fenestrated blood vessels in the rat choroid plexus are permeable to dye-labelled proteins, HRP and ferritin. Most leakage appears to be via fenestrae but some additional escape of marker appears to take place through transient and reversible openings in the junctions between endothelial cells. After they have escaped into the choroidal stroma markers are prevented from entering the CSF by tight junctions between the epithelial cells which cover the choroid plexus, but how they are removed from the extravascular space is not known. Electron microscope study of rats who have been given multiple intravenous injections of ferritin shows that extravascular ferritin is take up both by connective tissue cells in the choroidal stroma and by choroidal epithelial cells. The findings suggest that the ingested protein is subsequently broken down within lysosomal vacuoles in the cytoplasm of these cells. Such intracellular digestion may be the major means of controlling the protein content of the extravascular spaces of the choroid plexus.
大鼠脉络丛中的有孔血管对染料标记的蛋白质、辣根过氧化物酶(HRP)和铁蛋白具有通透性。大部分渗漏似乎是通过小孔进行的,但一些额外的标记物逸出似乎是通过内皮细胞之间连接处以短暂且可逆的开口发生的。标记物逸入脉络膜基质后,覆盖脉络丛的上皮细胞之间的紧密连接会阻止其进入脑脊液,但它们是如何从血管外间隙清除的尚不清楚。对多次静脉注射铁蛋白的大鼠进行电子显微镜研究表明,血管外铁蛋白被脉络膜基质中的结缔组织细胞和脉络膜上皮细胞摄取。这些发现表明,摄入的蛋白质随后在这些细胞细胞质中的溶酶体空泡内被分解。这种细胞内消化可能是控制脉络丛血管外间隙蛋白质含量的主要方式。