MiR-207/352 regulate lysosomal-associated membrane proteins and enzymes following ischemic stroke

J Tao1, W Liu1, G Shang2

  • 1College of Rehabilitation Medicine & TCM Rehabilitation Research Center Of SATCM, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, PR China.

Neuroscience
|August 2, 2015
PubMed

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.

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