Oxygen glucose deprivation-pretreated astrocyte-derived exosomes attenuates intracerebral hemorrhage (ICH)-induced BBB disruption through miR-27a-3p /ARHGAP25/Wnt/β-catenin axis

• Published in: Fluids and barriers of the CNS Vol. 21; no. 1; p. 8
• Main Authors: Hou, Ying, Xie, Ye, Liu, Xiaoxuan, Chen, Yushan, Zhou, Fangfang, Yang, Binbin
• Format: Journal Article
• Language: English
• Published: England BioMed Central 19.01.2024; BMC
• Subjects: Animals; Astrocytes; Astrocytes - metabolism; beta Catenin - metabolism; Blood brain barrier; Blood-Brain Barrier - metabolism; Brain; Brain injury; Cerebral Hemorrhage - metabolism; Endothelial Cells - metabolism; Exosomes; Exosomes - metabolism; Experiments; Glucose; Hemin; Hemorrhage; Immunofluorescence; Intracerebral hemorrhage; Laboratory animals; Manufacturers; Mice; MicroRNAs; MicroRNAs - genetics; MicroRNAs - metabolism; MicroRNAs - pharmacology; miR-27a-3p; miRNA; Neurological diseases; OGD pretreated astrocyte-derived exosome; Oxygen - metabolism; Paracrine signalling; Permeability; Proteins; Wnt protein; β-Catenin; miR-27a-3p; Blood brain barrier; Intracerebral hemorrhage; OGD pretreated astrocyte-derived exosome
• ISSN: 2045-8118; 2045-8118
• DOI: 10.1186/s12987-024-00510-2

Blood brain barrier (BBB) breakdown is one of the key mechanisms of secondary brain injury following intracerebral hemorrhage (ICH). Astrocytes interact with endothelial and regulate BBB integrity via paracrine signaling factors. More and more studies reveal astrocyte-derived extracellular vesicles (ADEVs) as an important way of intercellular communication. However, the role of ADEV in BBB integrity after ICH remains unclear. ADEVs were obtained from astrocytes with or without oxygen and glucose deprivation (OGD) pre-stimulation and the role of ADEVs in ICH was investigated using ICH mice model and ICH cell model. The potential regulatory effect of ADEVs on endothelial barrier integrity was identified by TEER, western blot and immunofluorescence in vitro. In vivo, functional evaluation, Evans-blue leakage and tight junction proteins (TJPs) expression were analyzed. MiRNA sequencing revealed that microRNA-27a-3p (miR-27a-3p) was differentially expressed miRNA in the EVs from OGD-pretreated astrocytes compared with normal control. The regulatory mechanism of miR-27a-3p was assessed using Luciferase assay, RT-PCR, western blot and immunofluorescence. OGD-activated astrocytes reduced hemin-induced endothelial hyper-permeability through secreting EVs. OGD-activated ADEVs alleviated BBB dysfunction after ICH in vivo and in vitro. MicroRNA microarray analysis indicated that miR-27a-3p is a major component that was highly expressed miRNA in OGD pretreated-ADEVs. OGD-ADEVs mitigated BBB injury through transferring miR-27a-3p into bEnd.3 cells and regulating ARHGAP25/Wnt/β-catenin pathway. Taken together, these findings firstly revealed that miR-27a-3p, as one of the main components of OGD-pretreated ADEVs, attenuated BBB destruction and improved neurological deficits following ICH by regulating endothelial ARHGAP25/Wnt/β-catenin axis. OGD-ADEVs might be a novel strategy for the treatment of ICH. this study implicates that EVs from OGD pre-stimulated astrocytes.