Schlosshauer B, Herzog K H
Max-Planck-Institut für Entwicklungsbiologie, Tübingen, Federal Republic of Germany.
J Cell Biol. 1990 Apr;110(4):1261-74. doi: 10.1083/jcb.110.4.1261.
The blood-brain barrier is characterized by still poorly understood barrier and transport functions performed by specialized endothelial cells. Hybridoma technology has been used to identify a protein termed neurothelin that is specific for these endothelial cells. Neurothelin is defined by the species-specific mouse mAb 1W5 raised against lentil-lectin-binding proteins of neural tissue from embryonic chick. In the posthatch chick, neurothelin expression is found on endothelial cells within the brain but not on those of the systemic vascular system. Injection of the monoclonal antibody in vivo leads to labeling of brain capillaries, indicating that the corresponding antigen is expressed on the luminal surface of brain endothelial cells. Transplantation of embryonic mouse brain onto the chick chorioallantoic membrane results in rodent brain vascularization by the avian vascular system. Subsequently, normally mAb 1W5-negative endothelial cells, originating from blood vessels of the chick chorioallantoic membrane, are induced to express neurothelin when they are in contact with mouse neural tissue. In contrast to differentiated brain neurons that do not express neurothelin, neurons of the nonvascularized chick retina synthesize neurothelin. However, neurothelin is not found on retinal ganglion cell axons terminating on 1W5-negative brain cells. 1W5 immunoreactivity was also found in the pigment epithelium that forms the blood-eye barrier. Putting epithelial cells into culture results in concentration of neurothelin at cell-cell contact sites, leaving other cell surface areas devoid of antigen. Therefore, the distribution of neurothelin appears to be regulated by cell-cell interactions. In Western blot analysis, neurothelin was identified as a protein with a molecular mass of approximately 43 kD. The protein bears at least one intramolecular disulfide bridge and sulfated glucuronic acid as well as alpha-D-substituted mannose/glucose moieties. The exclusive neurothelin expression in the posthatch chick on endothelial cells of the central nervous system but not on systemic endothelial cells makes neurothelin a marker specific for blood-brain barrier-forming endothelial cells. The spatiotemporally regulated neurothelin expression in neurons suggests an interaction between vascularization and neuronal differentiation.
血脑屏障的特点是由特化的内皮细胞执行的屏障和转运功能仍未被充分理解。杂交瘤技术已被用于鉴定一种名为神经鞘素的蛋白质,它对这些内皮细胞具有特异性。神经鞘素由针对胚胎鸡神经组织中扁豆凝集素结合蛋白产生的种属特异性小鼠单克隆抗体1W5定义。在孵化后的鸡中,神经鞘素表达于脑内的内皮细胞上,但在全身血管系统的内皮细胞上未发现。在体内注射单克隆抗体导致脑毛细血管被标记,表明相应抗原表达于脑内皮细胞的腔面。将胚胎小鼠脑移植到鸡绒毛尿囊膜上会导致啮齿动物脑由禽类血管系统血管化。随后,源自鸡绒毛尿囊膜血管的通常为单克隆抗体1W5阴性的内皮细胞,当它们与小鼠神经组织接触时会被诱导表达神经鞘素。与不表达神经鞘素的分化脑神经元不同,未血管化的鸡视网膜神经元合成神经鞘素。然而,在终止于单克隆抗体1W5阴性脑细胞的视网膜神经节细胞轴突上未发现神经鞘素。在形成血眼屏障的色素上皮中也发现了单克隆抗体1W5免疫反应性。将上皮细胞进行培养会导致神经鞘素在细胞间接触部位聚集,而其他细胞表面区域没有抗原。因此,神经鞘素的分布似乎受细胞间相互作用调节。在蛋白质印迹分析中,神经鞘素被鉴定为一种分子量约为43 kD的蛋白质。该蛋白质至少含有一个分子内二硫键以及硫酸化葡萄糖醛酸和α-D-取代的甘露糖/葡萄糖部分。孵化后鸡中枢神经系统内皮细胞而非全身内皮细胞中神经鞘素的独特表达使神经鞘素成为血脑屏障形成内皮细胞的特异性标志物。神经元中神经鞘素表达的时空调节表明血管化与神经元分化之间存在相互作用。