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Evaluating Cell Death Signaling by Immunofluorescence in a Rat Model of Ischemic Stroke
Published on: January 3, 2025
MiR-207/352 regulate lysosomal-associated membrane proteins and enzymes following ischemic stroke
1College of Rehabilitation Medicine & TCM Rehabilitation Research Center Of SATCM, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, PR China.
Abstract:
The role of microRNAs (miRNAs) in lysosome-mediated neuronal death and survival following ischemic stroke remains unknown. Herein, using miRNA and mRNA gene expression profiling microarrays, we identified the differentially expressed 24 miRNAs and 494 genes in the cortical peri-infarct area, respectively. Integrating the miRNA targets and mRNA expression profiles, we found 47 genes of miRNA targets, including lysosomal-associated membrane protein 2 (LAMP2), Hexb, Bcl2, etc. MiR-207 and miR-352 were mainly downregulated after ischemic stroke, followed by a slight return to baseline during post-middle cerebral artery occlusion (MCAO) 1d to 7d. Furthermore, the luciferase reporter assay demonstrated that LAMP2 and Hexb were the direct targets of miR-207 and miR-352, respectively. After lateral ventricle injection with miR-207 agonist mimics, the neurological deficit scores and infarct volumes were attenuated, and the structure of mitochondria ridges was improved. In addition, miR-207 mimics could reduce the number of cellular lysosome and autophagosome, whereas increase the number of autophagic vacuoles, indicating miR-207 might affect the latter part of lysosomal-autophagy pathway and mitochondria-induced apoptosis. These results suggested that miR-207 and miR-352 were involved in lysosomal pathway for mediating ischemic injury and spontaneous recovery. MiR-207 mimics as potential target drugs could protect against autophagic cell death after ischemic stroke.
Insights
MicroRNAs (miRNAs) miR-207 and miR-352 play a role in brain cell death after ischemic stroke. miR-207 mimics show potential for treating stroke by protecting against cell death.
Area of Science:
- Neuroscience
- Molecular Biology
- Genetics
Background:
- The role of microRNAs (miRNAs) in neuronal death and survival following ischemic stroke is not well understood.
- Lysosome-mediated cell death pathways are critical in ischemic stroke pathology.
Purpose of the Study:
- To investigate the role of specific miRNAs in lysosome-mediated neuronal death after ischemic stroke.
- To identify novel miRNA targets involved in ischemic injury and recovery.
Main Methods:
- Gene expression profiling (miRNA and mRNA microarrays) in the peri-infarct cortex.
- Luciferase reporter assays to validate miRNA-target interactions.
- In vivo studies using miR-207 agonist mimics in a middle cerebral artery occlusion (MCAO) model.
Main Results:
- Identified 24 differentially expressed miRNAs and 494 genes, including lysosomal-associated membrane protein 2 (LAMP2), Hexb, and Bcl2.
- miR-207 and miR-352 were downregulated post-ischemic stroke, targeting LAMP2 and Hexb, respectively.
- miR-207 mimics reduced infarct volume, improved mitochondrial structure, and modulated lysosomal-autophagy pathways, suggesting protection against cell death.
Conclusions:
- miR-207 and miR-352 are involved in the lysosomal pathway mediating ischemic injury and recovery.
- miR-207 mimics demonstrate therapeutic potential for protecting against autophagic cell death in ischemic stroke.

