Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, School of Future Technology, Peking University, Beijing 100871, China.
College of Future Technology, Peking University, Beijing 100871, China.
Cells. 2024 Oct 1;13(19):1635. doi: 10.3390/cells13191635.
Brain endothelial cells (ECs) are essential elements of the blood-brain barrier (BBB), maintaining its integrity through both paracellular junctions and transcellular transport systems. Myosin IIA, a multifunctional protein, plays a significant role in various cellular processes, including cytoskeletal maintenance, cell division, and signal transduction. While Myosin IIA has been implicated in bleeding and ischemic stroke, its role in regulating BBB integrity under physiological conditions remains unclear. In this study, we investigated the impact of Myosin IIA deficiency on BBB integrity using intravenous tracer injections and models of epilepsy. Flow cytometry, Western blot, and real-time PCR were employed to isolate brain cells and assess changes in protein and mRNA levels. Additionally, immunofluorescence staining and electron microscopy were used to explore alterations in protein expression and the structure of BBB. Our results demonstrate that endothelial Myosin IIA deficiency increased BBB permeability and exacerbated symptoms in BBB-related diseases. Mechanistically, we found that Myosin IIA modulates β-catenin transcription and protein interactions. The overexpression of β-catenin in brain endothelial Myosin IIA deficiency mice improved BBB integrity and reduced disease severity. This study establishes Myosin IIA as a critical regulator of BBB integrity and suggests new therapeutic targets for vascular diseases.
脑内皮细胞(ECs)是血脑屏障(BBB)的重要组成部分,通过细胞旁连接和细胞内转运系统维持其完整性。肌球蛋白 IIA 是一种多功能蛋白,在多种细胞过程中发挥重要作用,包括细胞骨架维持、细胞分裂和信号转导。虽然肌球蛋白 IIA 已被牵连到出血和缺血性中风中,但它在生理条件下调节 BBB 完整性的作用仍不清楚。在这项研究中,我们使用静脉内示踪剂注射和癫痫模型研究了肌球蛋白 IIA 缺乏对 BBB 完整性的影响。流式细胞术、Western blot 和实时 PCR 用于分离脑细胞并评估蛋白质和 mRNA 水平的变化。此外,免疫荧光染色和电子显微镜用于探索蛋白质表达和 BBB 结构的变化。我们的结果表明,内皮细胞肌球蛋白 IIA 缺乏会增加 BBB 通透性,并加重 BBB 相关疾病的症状。在机制上,我们发现肌球蛋白 IIA 调节 β-连环蛋白转录和蛋白相互作用。在脑内皮肌球蛋白 IIA 缺乏小鼠中过表达 β-连环蛋白可改善 BBB 完整性并减轻疾病严重程度。这项研究确立了肌球蛋白 IIA 作为 BBB 完整性的关键调节剂,并为血管疾病提供了新的治疗靶点。