The removal of axonal and myelin debris by macrophages is crucial for safeguarding nerves and facilitating functional recuperation in cerebral ischemic stroke. However, the physiological function of macrophage scavenger receptor 1 (MSR1) in ischemic white matter injury remains poorly de-fined. In this study, we observed an elevation in Msr1 expression levels in mice with experimental cerebral ischemic stroke. Msr 1-deficient (Msr1-/-) mice exhibited exacerbated behavioral deficits and aggravated white matter injury after ischemic stroke. Furthermore, the overexpression of Msr1 led to an increase in the phosphorylation of Akt via Hrh1, which in turn expedited the clearance of myelin debris through the PI3K/AKT pathway. In conclusion, our findings underscore the essential role of MSR1 in microglial phagocytosis and its ability to mitigate ischemic white matter injury in cerebral ischemic stroke.
Keyphrases
- white matter
- multiple sclerosis
- cerebral ischemia
- atrial fibrillation
- subarachnoid hemorrhage
- adipose tissue
- inflammatory response
- cell proliferation
- ischemia reperfusion injury
- poor prognosis
- spinal cord injury
- neuropathic pain
- traumatic brain injury
- high fat diet induced
- binding protein
- type diabetes
- blood brain barrier
- insulin resistance
- long non coding rna
- lps induced
- living cells
- sensitive detection
- single molecule
- fluorescent probe
- cerebral blood flow