首页> 美国卫生研究院文献>Biological Research >LncRNA SNHG14 promotes OGD/R-induced neuron injury by inducing excessive mitophagy via miR-182-5p/BINP3 axis in HT22 mouse hippocampal neuronal cells
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LncRNA SNHG14 promotes OGD/R-induced neuron injury by inducing excessive mitophagy via miR-182-5p/BINP3 axis in HT22 mouse hippocampal neuronal cells

机译:LNCRNA SNHG14通过在HT22小鼠海马神经元细胞中诱导MIR-182-5P / BINP3轴过量的影响促进OGD / R诱导的神经元损伤

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摘要

SNHG14 overexpression promotes apoptosis of OGD/R-induced HT22 cells. HT22 cell model was established by OGD/R treatment. Normal HT22 cells served as control. a QRT-PCR was performed to assess the expression of SNHG14 in the HT22 cells. HT22 cells were transfected with pcDNA3.1-SNHG14, pcDNA3.1-NC, si-SNHG14 or si-Ctrl. Then, the modified HT22 cells were subjected to OGD/R treatment. b QRT-PCR was performed to detect the expression of SNHG14 in the modified HT22 cells. c Flow cytometry was performed to explore the apoptosis of the modified HT22 cells. d The expression of caspase-3, cleaved-caspase-3, caspase-9 and cleaved-caspase-9 in the modified HT22 cells was examined by WB. (*P < 0.05, **P < 0.01, versus Control or Vector; #P < 0.05, ##P < 0.01, versus si-Ctrl)
机译:SNHG14过表达促进OGD / R诱导的HT22细胞的凋亡。 HT22细胞模型由OGD / R治疗建立。正常的HT22细胞用作控制。进行QRT-PCR以评估HT22细胞中SnHG14的表达。用PCDNA3.1-SNHG14,PCDNA3.1-NC,S1-SNHG14或Si-Ctrl转染HT22细胞。然后,对改性的HT22细胞进行OGD / R处理。进行B QRT-PCR以检测改性HT22细胞中SNHG14的表达。进行C流出细胞术以探讨改性HT22细胞的凋亡。 D通过Wb检查Caspase-3,切割的Caspase-3,Caspase-9和切割的-Caspase-9的表达。 (* p <0.05,** p <0.01,与控制或矢量; #p <0.05,## p <0.01,与Si-Ctrl)

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