Human Plasma-Derived Extracellular Vesicles Protect Against Cerebral Ischemia-Reperfusion Injury via HSP27 Phosphorylation

Ischemic stroke (IS) has become a serious public health problem, with patients undergoing endovascular treatment experiencing ischemia-reperfusion (I/R) injury, which exacerbates cerebrovascular diseases. Circulating extracellular vesicles (EVs) have shown potential for treating cerebral I/R injury. In this study, the therapeutic effect of human plasma-derived EVs and protective mechanisms in cerebral I/R injury is explored. An oxygen-glucose deprivation/reperfusion (OGD/R) model is used to treat SH-SY5Y cells in vitro, and an I/R injury model is constructed by transient middle cerebral artery occlusion (tMCAO) in mice. Human plasma-derived EVs are extracted by size exclusion chromatography. Western blot, Immunofluorescence Staining, and 2,3,5-Triphenyltetrazolium Chloride (TTC) Staining are employed to observe the effects of EVs on the neuroinflammatory response and infarct volumes in tMCAO mice, while TUNEL Staining, Flow Cytometry, and Western Blot are employed to assess cell apoptosis. Human plasma-derived EVs alleviated apoptosis in SH-SY5Y cells under OGD/R stress and exerted a protective effect against brain I/R injury in tMCAO mice. Mechanistically, EVs protected against cerebral I/R injury via HSP27 phosphorylation, and the HSP27 phosphorylation inhibitor KRIBB3 attenuated the anti-apoptotic effects of EVs. Human plasma-derived EVs activated the phosphorylation of HSP27, thereby inhibiting cell apoptosis and protecting against cerebral I/R injury. Human plasma-derived extracellular vesicles (EVs) mitigate the apoptosis of SH-SY5Y cells under oxygen glucose deprivation/reperfusion (OGD/R) stress and prevent neuronal apoptosis in transient middle cerebral artery occlusion (tMCAO) mice by regulating HSP27 phosphorylation. image