AI Article Synopsis

  • Post-stroke edema and upregulated aquaporin 4 (AQP4) channels contribute significantly to worsening stroke outcomes, while intra-arterial (IA) administration of mesenchymal stem cells (MSCs) has shown potential for neuroprotection and functional recovery.
  • The study investigates the role of protein kinase C delta (PKCδ) in mediating the effects of IA MSCs on AQP4 regulation and edema after a stroke in female rats, following the administration of MSCs shortly after stroke onset.
  • Results demonstrate that IA MSC treatment reduced brain injury and edema, improved functional outcomes, and altered the expression levels of PKCδ and AQP4, suggesting a novel mechanism of action for MSC therapy in

Article Abstract

Post-stroke edema and upregulation of aquaporin 4 (AQP4) water transport channels play a significant role in the progression of stroke pathology and deteriorating stroke outcomes. Prior studies from our lab have demonstrated the safety and efficacy of intra-arterial (IA) 1 × 10 mesenchymal stem cells (MSCs) administration post-stroke towards functional restoration and neuroprotection. Protein kinases have been reported to be involved in the signaling cascade of edema, with evidence supporting both its upregulation and downregulation at 24 h post-stroke. Among different protein kinase C (PKC) isoforms, the δ isoform is widely reported to play a pivotal role in the progression of ischemic reperfusion injury. Our present study aims to decipher the molecular mechanism of post-stroke IA MSCs mediated alleviation of perifocal vasogenic edema by PKCδ-mediated AQP4 regulation. Ovariectomized female SD rats were infused with 1 × 10 IA MSCs at 6 h post middle cerebral artery occlusion (MCAo). Animals were evaluated for behavioral and functional outcomes. Brains were harvested for evaluating infarct size and brain edema. Further, brain tissues were used for biochemical and molecular studies to decipher the possible molecular mechanism related to the regulation of PKCδ-mediated AQP4 expression. 1 × 10 IA MSCs at 6 h post-stroke confers neuroprotection as evident by the reduction in infarct size, edema, and improvement of functional outcome. An increase in GSH and catalase and a reduction in nitrite and MDA were observed along with a decrease in AQP4 and PKCδ expressions within the cortical brain regions of IA MSC-infused animals. The study gives preliminary evidence that IA MSCs administration post-stroke modulates PKCδ to regulate AQP4 expression which alleviates vasogenic edema towards neuroprotection. The study is novel and clinically relevant as no previous studies have looked into this aspect following IA delivery of stem cells in an animal model of ischemic stroke.

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Source
http://dx.doi.org/10.1007/s12035-022-02761-2DOI Listing

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