Robinson C S, Wagner R C
Microcirc Endothelium Lymphatics. 1985 Jun;2(3):313-29.
Plasma levels of lipoproteins are believed to be controlled largely by lipoprotein receptors on the surfaces of tissue cells which facilitate their internalization and degradation. This presupposes transit of lipoproteins across the walls of blood vessels in order to gain access to the receptor sites. The endothelium of tissue capillaries may therefore constitute an additional regulatory barrier for lipoproteins. In order to test this hypothesis, we have measured the uptake of fluorescent-labeled lipoproteins into endothelial vesicles of capillaries isolated from fat tissue. HDLs are ingested at more than twice the efficiency of LDLs and VLDLs are excluded from vesicular ingestion. This represents a decreased efficiency of ingestion with an increase in molecular diameter of lipoproteins. This phenomenon correlates well with the dimensions of endothelial vesicles and caveolae which may restrict entry of very large serum lipoproteins. Selective transport of lipoproteins by capillary endothelial vesicles on the basis of molecular size may therefore serve to regulate blood-tissue interchanges of lipid.
血浆脂蛋白水平被认为在很大程度上受组织细胞表面脂蛋白受体的控制,这些受体促进脂蛋白的内化和降解。这预先假定脂蛋白要穿过血管壁才能到达受体部位。因此,组织毛细血管的内皮可能构成脂蛋白的另一个调节屏障。为了验证这一假设,我们测量了从脂肪组织分离出的毛细血管内皮小泡对荧光标记脂蛋白的摄取。高密度脂蛋白(HDLs)的摄取效率是低密度脂蛋白(LDLs)的两倍多,极低密度脂蛋白(VLDLs)则被排除在小泡摄取之外。这表明随着脂蛋白分子直径的增加,摄取效率降低。这种现象与内皮小泡和小窝的尺寸密切相关,它们可能会限制非常大的血清脂蛋白进入。因此,基于分子大小的毛细血管内皮小泡对脂蛋白的选择性运输可能有助于调节血液与组织之间的脂质交换。