天津医药 ›› 2025, Vol. 53 ›› Issue (9): 903-909.doi: 10.11958/20251830

• 细胞与分子生物学 • 上一篇    下一篇

LncRNA SNHG14靶向miR-30a-5p对高糖诱导的足细胞损伤的影响

孔翠文(), 路延双, 孙丽萍, 于芬芬()   

  1. 康复大学青岛中心医院肾内科(邮编266000)
  • 收稿日期:2025-05-01 修回日期:2025-07-01 出版日期:2025-09-15 发布日期:2025-09-16
  • 通讯作者: E-mail:hzxyff@163.com
  • 作者简介:孔翠文(1986),女,主治医师,主要从事痛风性肾病方面研究。E-mail:zhutong89452@163.com

The effect of LncRNA SNHG14 on high glucose induced podocyte injury by targeting miR-30a-5p

KONG Cuiwen(), LU Yanshuang, SUN Liping, YU Fenfen()   

  1. Department of Nephrology, Qingdao Central Hospital, Rehabilitation University, Qingdao 266000, China
  • Received:2025-05-01 Revised:2025-07-01 Published:2025-09-15 Online:2025-09-16
  • Contact: E-mail: hzxyff@163.com

摘要:

目的 探究长链非编码RNA小核仁RNA宿主基因14(LncRNA SNHG14)靶向调控微小RNA-30a-5p(miR-30a-5p)对高糖诱导的足细胞损伤的影响。方法 体外培养足细胞,并将其分为标准糖(NG)组、高糖(HG)组、si-NC+HG组、si-SNHG14+HG组、miR-NC+HG组、miR-30a-5p mimics+HG组、si-SNHG14+inhibitor NC+HG组、si-SNHG14+miR-30a-5p inhibitor+HG组。实时荧光定量聚合酶链式反应(RT-qPCR)检测LncRNA SNHG14、miR-30a-5p表达;流式细胞术检测细胞凋亡;酶联免疫吸附试验(ELISA)检测肿瘤坏死因子-α(TNF-α)、白细胞介素(IL)-6、IL-1β水平;分别采用黄嘌呤氧化法、钼酸铵比色法、硫代巴比妥酸法检测超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、丙二醛(MDA)水平;双萤光素酶报告基因检测LncRNA SNHG14与miR-30a-5p的靶向关系;Western blot检测凋亡相关蛋白表达。结果 与NG组相比,HG组LncRNA SNHG14表达、细胞凋亡率、TNF-α、IL-6、IL-1β、MDA水平升高,miR-30a-5p表达、SOD、CAT水平降低(P<0.05)。与HG组、si-NC+HG组相比,si-SNHG14+HG组LncRNA SNHG14表达、细胞凋亡率、TNF-α、IL-6、IL-1β、MDA水平、Bcl-2相关X蛋白(Bax)、活化型胱天蛋白酶-3(cleaved caspase-3)蛋白表达水平降低,miR-30a-5p表达、SOD、CAT水平、B细胞淋巴瘤-2蛋白(Bcl-2)表达水平升高(P<0.05);与HG组、miR-NC+HG组相比,miR-30a-5p mimics+HG组LncRNA SNHG14表达无变化(P>0.05),miR-30a-5p表达、SOD、CAT水平、Bcl-2蛋白表达升高,细胞凋亡率、TNF-α、IL-6、IL-1β、MDA水平、Bax、cleaved caspase-3蛋白表达水平降低(P<0.05);与si-SNHG14+HG组、si-SNHG14+inhibitor NC+HG组相比,si-SNHG14+miR-30a-5p inhibitor+HG组LncRNA SNHG14表达无变化(P>0.05),miR-30a-5p表达、SOD、CAT水平、Bcl-2蛋白表达水平降低,细胞凋亡率、TNF-α、IL-6、IL-1β、MDA水平、Bax、cleaved caspase-3蛋白表达水平升高(P<0.05)。双萤光素酶报告基因实验证实LncRNA SNHG14靶向负调控miR-30a-5p。结论 抑制LncRNA SNHG14可靶向miR-30a-5p减轻高糖诱导的足细胞损伤。

关键词: 糖尿病肾病, 足细胞, 细胞凋亡, 炎症, LncRNA SNHG14, miR-30a-5p, 高糖

Abstract:

Objective To investigate the effect of long non-coding RNA small nucleolar RNA host gene 14 (LncRNA SNHG14) on high glucose-induced podocyte injury by targeting microRNA-30a-5p (miR-30a-5p). Methods Podocytes were cultured in vitro and were divided into the following groups: the standard glucose (NG) group, the high glucose (HG) group, the si-NC+HG group, the si-SNHG14+HG group, the miR-NC+HG group, the miR-30a-5p mimics+HG group, the si-SNHG14+inhibitor NC+HG group and the si-SNHG14+miR-30a-5p inhibitor+HG group. Quantitative real-time polymerase chain reaction (RT-qPCR) was performed to detect expression levels of LncRNA SNHG14 and miR-30a-5p. Flow cytometry was used to determine cell apoptosis. Enzyme-linked immunosorbent assay (ELISA) was applied to measure levels of tumor necrosis factor-alpha (TNF-α), interleukin (IL)-6 and IL-1β. Xanthine oxidase method, ammonium molybdate colorimetry and thiobarbituric acid method were respectively used to detect superoxide dismutase (SOD), catalase (CAT) and malondialdehyde (MDA). Dual-luciferase reporter gene was conducted to verify the targeting relationship between LncRNA SNHG14 and miR-30a-5p. Western blot assay was performed to detect expression levels of apoptosis-related proteins. Results Compared with the NG group, the HG group exhibited increased expression levels of LncRNA SNHG14, cell apoptosis rate, as well as levels of TNF-α, IL-6, IL-1β and MDA, whereas the expression level of miR-30a-5p and levels of SOD and CAT were decreased (P<0.05). Compared with the HG group and the si-NC+HG group, the si-SNHG14+HG group exhibited decreased expression levels of LncRNA SNHG14, apoptosis rate, levels of TNF-α, IL-6, IL-1β and MDA, as well as expression levels of Bax and cleaved caspase-3 proteins, while the expression level of miR-30a-5p, levels of SOD and CAT and the expression level of Bcl-2 protein were increased (P<0.05). Compared with the HG group and the miR-NC+HG group, the miR-30a-5p mimics+HG group showed no significant difference in the expression level of LncRNA SNHG14 (P>0.05). Meanwhile, the expression level of miR-30a-5p, levels of SOD and CAT, and expression level of Bcl-2 protein were increased, whereas the cell apoptosis rate, levels of TNF-α, IL-6, IL-1β and MDA, as well as expression levels of Bax and cleaved caspase-3 proteins were decreased (P<0.05). Compared with the si-SNHG14+HG group and the si-SNHG14+inhibitor NC+HG group, the si-SNHG14+miR-30a-5p inhibitor+HG group showed no significant difference in the expression level of LncRNA SNHG14 (P>0.05), meanwhile, the expression level of miR-30a-5p, levels of SOD and CAT, and expression level of Bcl-2 protein were reduced, whereas the cell apoptosis rate, levels of TNF-α, IL-6, IL-1β and MDA, as well as expression levels of Bax and cleaved caspase-3 proteins were increased (P<0.05). The dual-luciferase reporter gene assay confirmed that LncRNA SNHG14 targeted and negatively regulated miR-30a-5p. Conclusion The inhibition of LncRNA SNHG14 can target miR-30a-5p to alleviate high glucose induced podocyte injury.

Key words: diabetic nephropathies, podocytes, apoptosis, inflammation, LncRNA SNHG14, miR-30a-5p, high glucose

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