4.7 Article

CD11c+ microglia promote white matter repair after ischemic stroke

Journal

CELL DEATH & DISEASE
Volume 14, Issue 2, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s41419-023-05689-0

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Ischemic stroke leads to white matter damage and neurological deficits. In this study, the characteristics of white matter injury and repair after stroke were investigated using a mouse stroke model. The researchers found that white matter damage was most severe on Day 7 after the stroke, and gradually recovered from Day 7 to Day 30. They also discovered that CD11c(+) microglia play critical roles in white matter repair and functional recovery after stroke. These findings suggest that spontaneous white matter repair occurs after ischemic stroke, with CD11c(+) microglia being key players in this restorative process.
Ischemic stroke leads to white matter damage and neurological deficits. However, the characteristics of white matter injury and repair after stroke are unclear. Additionally, the precise molecular communications between microglia and white matter repair during the stroke rehabilitation phase remain elusive. In this current study, MRI DTI scan and immunofluorescence staining were performed to trace white matter and microglia in the mouse transient middle cerebral artery occlusion (tMCAO) stroke model. We found that the most serious white matter damage was on Day 7 after the ischemic stroke, then it recovered gradually from Day 7 to Day 30. Parallel to white matter recovery, we observed that microglia centered around the damaged myelin sheath and swallowed myelin debris in the ischemic areas. Then, microglia of the ischemic hemisphere were sorted by flow cytometry for RNA sequencing and subpopulation analysis. We found that CD11c(+) microglia increased from Day 7 to Day 30, demonstrating high phagocytotic capabilities, myelin-supportive genes, and lipid metabolism associated genes. CD11c(+) microglia population was partly depleted by the stereotactic injecting of rAAV2/6M-taCasp3 (rAAV2/6M-CMV-DIO-taCasp3-TEVp) into CD11c-cre mice. Selective depletion of CD11c(+) microglia disrupted white matter repair, oligodendrocyte maturation, and functional recovery after stroke by Rotarod test, Adhesive Removal test, and Morris Water Maze test. These findings suggest that spontaneous white matter repair occurs after ischemic stroke, while CD11c(+) microglia play critical roles in this white matter restorative progress.

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