Background
Ischemic stroke is a leading cause of disability and death worldwide, with limited treatment options, leaving many survivors with long-term neurological issues. Bone marrow mesenchymal stem cells (BMSCs) show promise in improving recovery, but few studies have examined their role during the recovery phase. This present study aims to explore whether and how BMSCs improve neurological function during the recovery period of ischemic stroke(IS).
Methods
Male Sprague-Dawley rats (weighing 280-300g) underwent transient middle cerebral artery occlusion(tMCAO). BMSCs and Bone marrow mesenchymal stem cell exosomes (BMSC-Exos) were isolated and characterized by flow cytometry, transmission electron microscopy, and western blotting assay. Neurological function was assessed through postural reflex, tactile, visual, proprioceptive placing tests, rotarod test, and Morris water maze. Angiogenesis and neurogenesis were observed by immunofluorescence staining (IF). Exosomal miRNA profiling was performed using a microRNA array. For the mechanism study, BMSCs + miR-195 CRISPR or BMSCs + miR-195 agomirs were administered intracerebroventricularly. Genes and protein expression levels were measured using qRT-qPCR, Western blotting, and IF staining.
Results
BMSCs enhance neurological function by promoting angiogenesis and neurogenesis during ischemic stroke recovery. MiR-195-5p, derived from BMSC exosomes, reduces Nogo-A induced by cerebral ischemia. Mechanistically, miR-195-5p stimulates vascular regeneration by inhibiting the Nogo-A/S1PR2 signaling pathway. Additionally, miR-195-5p inhibits the Nogo-A/NgR1 pathway, promoting neurogenesis.
Conclusions
BMSCs inhibit the Nogo-A/NgR1/S1PR2 signaling pathway via exosomal miR-195, promoting neurogenesis and angiogenesis during the ischemic stroke recovery phase, thereby reducing neurological deficits. These findings suggest that targeting Nogo-A with BMSCs during stroke recovery offers a promising therapeutic approach for survivors.