Department of Physiology and Pharmacology, Loma Linda University, School of Medicine, Loma Linda, CA, USA
Department of Neurology, Zhujiang Hospital, Southern Medical University, Guangzhou, China
Curr Neuropharmacol. 2020;18(12):1237-1249. doi: 10.2174/1570159X18666200529150907.
It is well-known that stroke is one of the leading causes of death and disability all over the world. After a stroke, the blood-brain barrier subsequently breaks down. The BBB consists of endothelial cells surrounded by astrocytes. Microglia, considered the long-living resident immune cells of the brain, play a vital role in BBB function. M1 microglia worsen BBB disruption, while M2 microglia assist in repairing BBB damage. Microglia can also directly interact with endothelial cells and affect BBB permeability. In this review, we are going to discuss the mechanisms responsible for the dual role of microglia in BBB dysfunction after stroke.
众所周知,中风是全世界导致死亡和残疾的主要原因之一。中风后,血脑屏障随后会破裂。血脑屏障由被星形胶质细胞包围的内皮细胞组成。小胶质细胞被认为是大脑中寿命较长的常驻免疫细胞,在 BBB 功能中起着至关重要的作用。M1 小胶质细胞使 BBB 破坏恶化,而 M2 小胶质细胞则有助于修复 BBB 损伤。小胶质细胞还可以直接与内皮细胞相互作用并影响 BBB 的通透性。在这篇综述中,我们将讨论导致小胶质细胞在中风后 BBB 功能障碍中发挥双重作用的机制。