Astrocytic Extracellular Vesicles Regulated by Microglial Inflammatory Responses Improve Stroke Recovery.
Chikage KijimaToshiki InabaKenichiro HiraNobukazu MiyamotoKazuo YamashiroTakao UrabeNobutaka HattoriYuji UenoPublished in: Molecular neurobiology (2023)
There are no effective treatments for post-stroke glial scar formation, which inhibits axonal outgrowth and functional recovery after stroke. We investigated whether astrocytic extracellular vesicles (AEVs) regulated by microglia modulate glial scars and improve stroke recovery. We found that peri-infarct glial scars comprised reactive astrocytes with proliferating C3d and decreased S100A10 expression in chronic stroke. In cultured astrocytes, microglia-conditioned media and treatment with P2Y 1 receptor antagonists increased and reduced the area of S100A10- and C3d-expressing reactive astrocytes, respectively, by suppressing mitogen-activated protein kinase/nuclear factor-κβ (NF-κB)/tumor necrosis factor-α (TNF-α)/interleukin-1β signaling after oxygen-glucose deprivation. Intracerebral administrations of AEVs enriched miR-146a-5p, downregulated NF-κB, and suppressed TNF-α expressions, by transforming reactive astrocytes to those with S100A10 preponderance, causing functional recovery in rats subjected to middle cerebral artery occlusion. Modulating neuroinflammation in post-stroke glial scars could permit axonal outgrowth, thus providing a basis for stroke recovery with neuroprotective AEVs.
Keyphrases
- neuropathic pain
- nuclear factor
- atrial fibrillation
- lps induced
- spinal cord injury
- middle cerebral artery
- inflammatory response
- cerebral ischemia
- signaling pathway
- rheumatoid arthritis
- toll like receptor
- spinal cord
- platelet rich plasma
- oxidative stress
- heart failure
- traumatic brain injury
- endothelial cells
- poor prognosis
- internal carotid artery
- tyrosine kinase
- immune response
- acute myocardial infarction
- pi k akt
- cell proliferation
- brain injury
- high resolution
- acute coronary syndrome
- weight loss
- binding protein
- optical coherence tomography
- left ventricular