Skutelsky E, Danon D
J Cell Biol. 1976 Oct;71(1):232-41. doi: 10.1083/jcb.71.1.232.
The ability of anionic groups on the luminal surface of blood vessels to redistribute by lateral migration under the influence of multivalent ligands was analyzed by electron microscopy, using cationized ferritin (CF). In vitro interaction of blood vessel segments with CF results in rapid aggregation of most anionic sites on the luminal fromt of the endothelium, followed by internalization or detachment of the CF patches, leaving most of the luminal surface devoid of anionic sites. Further incubation of such endothelial cells without CF results in regeneration of binding capacity for the polycationic label. Transport of CF, but not of native ferritin, across the endothelium by vesicle transport, followed by exocytosis of the interiorized CF clusters on the tissue front of the endothelium, was also observed. The possibility that such activities in the blood vessels in vivo may be associated with local changes in the normal distribution of the surface anionic sites as well as in accumulation of debris in the subendothelial layers of the vessels is suggested.
利用阳离子铁蛋白(CF)通过电子显微镜分析了血管腔表面阴离子基团在多价配体影响下通过侧向迁移进行重新分布的能力。血管段与CF的体外相互作用导致内皮腔面大多数阴离子位点迅速聚集,随后CF斑块内化或脱离,使大部分腔面没有阴离子位点。这种无CF的内皮细胞进一步孵育会导致对聚阳离子标记物结合能力的再生。还观察到CF通过囊泡运输穿过内皮,而天然铁蛋白则不能,随后内化的CF簇在内皮组织面胞吐。提示体内血管中的这种活动可能与表面阴离子位点正常分布的局部变化以及血管内皮下层碎片的积累有关。