Dehouck B, Dehouck M P, Fruchart J C, Cecchelli R
Institut National de la Santé et de la Recherche Médicale U325 Service d'Etude et de Recherche sur les Lipoprotéines et l'Atherosclérose, Institut Pasteur, Lille, France.
J Cell Biol. 1994 Jul;126(2):465-73. doi: 10.1083/jcb.126.2.465.
In contrast to the endothelial cells in large vessels where LDL receptors are downregulated, brain capillary endothelial cells in vivo express an LDL receptor. Using a cell culture model of the blood-brain barrier consisting of a coculture of brain capillary endothelial cells and astrocytes, we observed that the capacity of endothelial cells to bind LDL is enhanced threefold when cocultured with astrocytes. We next investigated the ability of astrocytes to modulate endothelial cell LDL receptor expression. We have shown that the lipid requirement of astrocytes increases the expression of endothelial cell LDL receptors. Experiments with dialysis membranes of different pore size showed that this effect is mediated by a soluble factor(s) with relative molecular mass somewhere between 3,500 and 14,000. Substituting astrocytes with smooth muscle cells or brain endothelium with endothelium from the aorta or the adrenal cortex did not enhance the luminal LDL receptor expression on endothelial cells, demonstrating the specificity of the interactions. This factor(s) is exclusively secreted by astrocytes cocultured with brain capillary endothelial cells, but it also upregulates the LDL receptor on other cell types. This study confirms the notion that the final fine tuning of cell differentiation is under local control.
与大血管中低密度脂蛋白(LDL)受体下调的内皮细胞不同,体内脑毛细血管内皮细胞表达LDL受体。利用由脑毛细血管内皮细胞和星形胶质细胞共培养组成的血脑屏障细胞培养模型,我们观察到与星形胶质细胞共培养时,内皮细胞结合LDL的能力增强了三倍。接下来,我们研究了星形胶质细胞调节内皮细胞LDL受体表达的能力。我们已经表明,星形胶质细胞的脂质需求增加了内皮细胞LDL受体的表达。用不同孔径的透析膜进行的实验表明,这种效应是由相对分子质量在3500至14000之间的一种或多种可溶性因子介导的。用平滑肌细胞替代星形胶质细胞,或用主动脉或肾上腺皮质的内皮细胞替代脑内皮细胞,均未增强内皮细胞腔面LDL受体的表达,这证明了相互作用的特异性。这种因子仅由与脑毛细血管内皮细胞共培养的星形胶质细胞分泌,但它也上调其他细胞类型上的LDL受体。这项研究证实了细胞分化的最终微调受局部控制这一观点。