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Elevated expression of lncRNA SNHG15 in spinal tuberculosis: preliminary results

机译:LNCrNA SnHG15在脊柱结核中的表达升高:初步结果

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OBJECTIVE: The incidence and disability rate of spinal tuberculosis is high. The role of the expression of lncRNA SNHG15 in spinal tuberculosis and related mechanisms remains unclear. PATIENTS AND METHODS: Spinal tuberculosis and normal control tissues were collected, and lncRNA SNHG15 level was analyzed by real-time PCR. Mouse RAW264.7 cells were cultured and divided into control group, tuberculin (PPD) group, si-SNHG15, and PPD+ si-SNHG15 group followed by analysis of lncRNA SNHG15 level, cell proliferation by MTT assay, formation of osteoclasts by TRAP staining, levels of interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α) by ELISA, as well as expression of RANK and RANKL by Western blot. RESULTS: The lncRNA SNHG15 expression in spinal tuberculosis tissues was significantly increased compared with that in the control group (p 0.05). The expression of lncRNA SNHG15 was increased in RAW264.7 cells in the PPD group with increased cell proliferation, TRAP-positive cells, IL-6 and TNF-α secretion, as well as elevated RANK and RANKL expression which were statistically different compared with the control group (p 0.05). Transfection of lncRNA SNHG15 siRNA in the PPD model significantly inhibited the expression of lncRNA SNHG15, decreased cell proliferation, TRAP staining positive cells, IL-6 and TNF-α secretion, as well as reduced RANK and RANKL expression. Compared with the PPD group, the differences were statistically significant (p 0.05). CONCLUSIONS: The expression of lncRNA SNHG15 was significantly increased in spinal tuberculosis tissues. The downregulation of lncRNA SNHG15 expression could inhibit the secretion of inflammatory cytokines by regulating the RANK/RANKL pathway, thereby regulating osteoclasts.
机译:目的:脊髓结核病的发病率和残疾率高。 LNCRNA SnHG15在脊柱结核和相关机制中表达的作用仍不清楚。患者和方法:收集脊柱结核和正常对照组织,通过实时PCR分析LNCRNA SNHG15水平。将小鼠Raw264.7细胞培养并分为对照组,结核菌素(PPD)基团,Si-SnHG15和PPD + Si-SnHG15组,然后分析LNCRNA SnHG15水平,MTT测定细胞增殖,通过捕获染色形成骨细胞, ELISA的白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)的水平,以及蛋白质印迹的等级和RANKL的表达。结果:与对照组相比,脊髓结核组织中的LNCrNA SnHG15表达显着增加(P <0.05)。在PPD组中的RANCRNA SNHG15中的表达增加,具有增加的细胞增殖,捕获阳性细胞,IL-6和TNF-α分泌,以及与统计学上的升高的等级和RANKL表达。对照组(P <0.05)。 PPD模型中LNCRNA SNHG15 siRNA的转染显着抑制LNCRNA SNHG15的表达,降低细胞增殖,捕获染色阳性细胞,IL-6和TNF-α分泌,以及降低的等级和RANKL表达。与PPD组相比,差异有统计学意义(P <0.05)。结论:LNCrNA SnHG15的表达在脊柱结核组织中显着增加。通过调节等级/ RANKL途径,LNCRNA SNHG15表达的下调可以抑制炎性细胞因子的分泌,从而调节破骨细胞。

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