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首页|期刊导航|中国免疫学杂志|LncRNA MEG3靶向miR-138-5p对肺炎链球菌诱导的人肺泡上皮细胞损伤的影响

LncRNA MEG3靶向miR-138-5p对肺炎链球菌诱导的人肺泡上皮细胞损伤的影响

孔维康 朱慧敏 张婵 王军

中国免疫学杂志2026,Vol.42Issue(8):1840-1846,7.
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中国免疫学杂志2026,Vol.42Issue(8):1840-1846,7.DOI:10.3969/j.issn.1000-484X.2026.08.008

LncRNA MEG3靶向miR-138-5p对肺炎链球菌诱导的人肺泡上皮细胞损伤的影响

Effect of LncRNA MEG3 on Streptococcus pneumoniae induced human alveolar epithelial cells damage by targeting miR-138-5p

孔维康 1朱慧敏 2张婵 3王军2

作者信息

  • 1. 滕州市中心人民医院新生儿科一病区,滕州 277500
  • 2. 滕州市中心人民医院儿童重症监护病房,滕州 277500
  • 3. 菏泽医学专科学校儿科教研室,菏泽 274000
  • 折叠

摘要

Abstract

Objective:To investigate effect of long non-coding RNA maternally expressed gene 3(LncRNA MEG3)on apopto-sis and inflammatory damage of human pulmonary alveolar epithelial cells(HPAEpiC)induced by Streptococcus pneumoniae(SP)by targeting miR-138-5p.Methods:A pneumonia cell model was established in vitro by inducing HPAEpiC with SP,LncRNA MEG3 and miR-138-5p expressions were detected by qRT-PCR.HPAEpiC were grouped into Control group,Model group,sh-NC group,sh-MEG3 group,sh-MEG3+inhibitor NC group,sh-MEG3+miR-138-5p inhibitor group,miR-NC group and miR-138-5p group.qRT-PCR was used to detect LncRNA MEG3 and miR-138-5p expressions of HPAEpiC in each group;CCK-8 kit was used to detect proliferation ability;flow cytometry was used to detect apoptosis;ELISA was used to detect inflammatory factor levels;Western blot was used to detect Bax and Bcl2 proteins expressions.Targeting relationship between LncRNA MEG3 and miR-138-5p was validated.Results:Compared with Control group,LncRNA MEG3 expression,Bax protein expression,apoptosis rate,IL-6,TNF-α levels in HPAEpiC were unusually increased in Model group,while miR-138-5p expression,Bcl-2 protein expression,cell viability and IL-10 level were unusually decreased(P<0.05).Compared with sh-NC group,LncRNA MEG3 expression,Bax protein expression,apopto-sis rate,IL-6,TNF-α levels in HPAEpiC were prominently decreased in sh-MEG3 group,while miR-138-5p expression,Bcl2 protein expression,cell viability and IL-10 level were prominently increased(P<0.05).Compared with sh-MEG3+inhibitor NC group,Bax protein expression,apoptosis rate,IL-6,TNF-α levels in HPAEpiC were unusually increased in sh-MEG3+miR-138-5p inhibitor group,while cell viability,Bcl2 protein expression and IL-10 level were unusually decreased(P<0.05).Compared with miR-NC group,Bcl2 protein expression and IL-10 level in HPAEpiC were prominently increased in miR-138-5p group,while Bax protein expression,TNF-α,IL-6 levels and apoptosis rate were prominently decreased(P<0.05).Further experiment verified targeting rela-tionship between LncRNA MEG3 and miR-138-5p.Conclusion:LncRNA MEG3 is overexpressed in SP induced HPAEpiC.Knocking down LncRNA MEG3 inhibits HPAEpiC inflammatory response and apoptosis by up-regulating miR-138-5p.

关键词

长链非编码RNA母系表达基因3/miR-138-5p/肺炎链球菌/人肺泡上皮细胞/炎症/凋亡

Key words

Long non-coding RNA maternally expressed gene 3/miR-138-5p/Streptococcus pneumoniae/Human pulmonary alveolar epithelial cells/Inflammation/Apoptosis

分类

医药卫生

引用本文复制引用

孔维康,朱慧敏,张婵,王军..LncRNA MEG3靶向miR-138-5p对肺炎链球菌诱导的人肺泡上皮细胞损伤的影响[J].中国免疫学杂志,2026,42(8):1840-1846,7.

中国免疫学杂志

1000-484X

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