Abstract
Summary: Aims: To explore the role and underlying mechanism of miR-124 in stroke. Methods: miR-124 expression was determined by real-time PCR. The effect of miR-124 on infarct area was assessed in middle cerebral artery occlusion (MCAO) mice. The influence of miR-124 on oxygen and glucose deprivation (OGD) induced neuron apoptosis and death was examined by immunofluorescence. The effect of miR-124 on apoptosis-related proteins was determined by Western blot. Results: The level of miR-124 is significantly increased in ischemic penumbra as compared with that in nonischemic area of MACO mice. Brain tissue of stroke-prone spontaneously hypertensive rats (SHR-SP) also showed higher level of miR-124 as compared with that of spontaneously hypertensive rats (SHR). Consistently, OGD treatment obviously increased miR-124 level in primary neurons. In vivo, miR-124 overexpression significantly decreased, while miR-124 knockdown significantly increased, the infarct area of MCAO mice. In vitro, gain or loss of miR-124 function resulted in reduced or increased neuron apoptosis and death induced by OGD, and increased or reduced antiapoptosis protein, Bcl-2 and Bcl-xl, respectively. Conclusions: miR-124 plays a neurons-protective role via apoptosis-inhibiting pathway in ischemic stroke. © 2013 John Wiley & Sons Ltd.
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Sun, Y., Gui, H., Li, Q., Luo, Z. M., Zheng, M. J., Duan, J. L., & Liu, X. (2013). MicroRNA-124 protects neurons against apoptosis in cerebral ischemic stroke. CNS Neuroscience and Therapeutics, 19(10), 813–819. https://doi.org/10.1111/cns.12142
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