Molecular Neurodegeneration, Institute for Pathobiochemistry, University Medical Center of the Johannes Gutenberg University of Mainz, Duesbergweg 6, 55099, Mainz, Germany.
Fluids Barriers CNS. 2021 Jun 19;18(1):27. doi: 10.1186/s12987-021-00260-5.
The entry of blood-borne molecules into the brain is restricted by the blood-brain barrier (BBB). Various physical, transport and immune properties tightly regulate molecule movement between the blood and the brain to maintain brain homeostasis. A recent study utilizing a pan-endothelial, constitutive Tie2-Cre showed that paracellular passage of blood proteins into the brain is governed by endocytic and cell signaling protein low-density lipoprotein receptor-related protein 1 (LRP1). Taking advantage of conditional Slco1c1-CreER specific to CNS endothelial cells and choroid plexus epithelial cells we now supplement previous results and show that brain endothelial Lrp1 ablation results in protease-mediated tight junction degradation, P-glycoprotein (P-gp) reduction and a loss of BBB integrity.
血液源性分子进入大脑受到血脑屏障(BBB)的限制。各种物理、转运和免疫特性严格调节血液和大脑之间分子的运动,以维持大脑内环境的稳定。最近的一项研究利用泛内皮细胞组成型 Tie2-Cre 发现,血液蛋白通过细胞旁途径进入大脑受内吞作用和细胞信号转导蛋白低密度脂蛋白受体相关蛋白 1(LRP1)的控制。利用 CNS 内皮细胞和脉络丛上皮细胞特异性条件性 Slco1c1-CreER,我们现在补充以前的结果,并表明脑内皮细胞 Lrp1 缺失导致蛋白酶介导的紧密连接降解、P 糖蛋白(P-gp)减少以及 BBB 完整性丧失。