Institute of Biomedical and Pharmaceutical Sciences, Guangdong University of Technology, Guangzhou, 510006, China.
Department of Pharmacy, The Third People's Hospital of Kunming, Kunming, 650000, China.
Mol Neurobiol. 2022 Feb;59(2):1073-1087. doi: 10.1007/s12035-021-02648-8. Epub 2021 Nov 27.
Increasing research has proved that long non-coding RNAs (lncRNAs) play a critical role in a variety of biological processes. However, their functions in cerebral ischemia are still unclear. We found that the small nucleolar RNA host gene 12 (SNHG12) is a new type of lncRNA induced by ischemia/reperfusion. Here, we show that the expression of SNHG12 was upregulated in the brain tissue of mice exposed to middle cerebral artery occlusion/reperfusion (MCAO/R) and primary mouse cerebral cortex neurons treated with oxygen-glucose deprivation/reoxygenation (OGD/R). Mechanistically, SNHG12 knockdown resulted in larger infarct sizes and worse neurological scores in MCAO/R mice. Consistent with the in vivo results, SNHG12 upregulation significantly increased the viability and prevented apoptosis of neurons cultured under OGD/R conditions. In addition, we found that SNHG12 acts as a competing endogenous RNA (ceRNA) with microRNA (miR)-136-5p, thereby regulating the inhibition of its endogenous target Bcl-2. Moreover, SNHG12 was proven to target miR-136-5p, increasing Bcl-2 expression, which finally led to the activation of PI3K/AKT signaling. In conclusion, we demonstrated that SNHG12 acts as a ceRNA of miR-136-5p, thereby targets and regulates the expression of Bcl-2, which attenuates cerebral ischemia/reperfusion injury via activation of the PI3K/AKT pathway. This knowledge helps to better understand the pathophysiology of cerebral ischemic stroke and may provide new treatment options for this disease.
越来越多的研究证明,长非编码 RNA(lncRNA)在多种生物过程中发挥着关键作用。然而,它们在脑缺血中的功能尚不清楚。我们发现,核仁小分子 RNA 宿主基因 12(SNHG12)是一种由缺血/再灌注诱导的新型 lncRNA。在这里,我们显示 SNHG12 的表达在经历大脑中动脉闭塞/再灌注(MCAO/R)的小鼠脑组织和接受氧葡萄糖剥夺/再氧合(OGD/R)处理的原代小鼠大脑皮质神经元中上调。从机制上讲,SNHG12 敲低导致 MCAO/R 小鼠的梗塞面积增大和神经评分恶化。与体内结果一致,SNHG12 的上调显著增加了 OGD/R 条件下培养的神经元的活力并防止了其凋亡。此外,我们发现 SNHG12 作为 microRNA(miR)-136-5p 的竞争性内源 RNA(ceRNA)发挥作用,从而调节其内源性靶标 Bcl-2 的抑制。此外,已经证明 SNHG12 靶向 miR-136-5p,增加 Bcl-2 的表达,最终导致 PI3K/AKT 信号通路的激活。总之,我们证明 SNHG12 作为 miR-136-5p 的 ceRNA,从而靶向并调节 Bcl-2 的表达,通过激活 PI3K/AKT 通路减轻脑缺血/再灌注损伤。这一知识有助于更好地理解脑缺血性中风的病理生理学,并可能为这种疾病提供新的治疗选择。