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环状 RNA circ_0130438 通过调控 miR-130a-3p/KLF9 轴抑制 TNF-α诱导的人成纤维样 MH7A 滑膜细胞增殖、迁移、侵袭和炎症反应。

Circular RNA circ_0130438 suppresses TNF-α-induced proliferation, migration, invasion and inflammation in human fibroblast-like MH7A synoviocytes by regulating miR-130a-3p/KLF9 axis.

机构信息

Department of Joint Surgery Treatment Center, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi City, Hubei Province, China.

Department of Orthopedics, Weihaiwei People's Hospital, Weihai City, Shandong Province, China.

出版信息

Transpl Immunol. 2022 Jun;72:101588. doi: 10.1016/j.trim.2022.101588. Epub 2022 Mar 28.

Abstract

BACKGROUND

Circular RNAs (circRNAs) can play a critical role in rheumatoid arthritis (RA) pathogenesis by involving gene regulation by competing for shared microRNAs (miRNAs), a family of small noncoding RNAs. MiR-130a-3p is a disease-related miRNA and Kruppel-like factor 9 (KLF9) is a zinc finger transcription factor, which are involved in RA pathogenesis. Here, we identified the action of circRNA circ_0130438 in regulating fibroblast-like synoviocytes (FLSs) stimulated by tumor necrosis factor α (TNF-α).

METHODS

The direct relationship between miR-130a-3p and circRNA circ_0130438 or KLF9 was predicted by bioinformatics analysis and examined by a dual-luciferase reporter or RNA immunoprecipitation (RIP) assay. CircRNA circ_0130438, miR-130a-3p and KLF9 factor expression levels were gauged by a quantitative real-time PCR (qRT-PCR) or a western blot method. Cell proliferation ability was analyzed by a 5-Ethynyl-2'-Deoxyuridine (EdU) staining assay. The transwell assay was used to evaluate cell migration and invasion capacities. The production levels of interleukin-1β (IL)-1β, IL-6 and IL-8 were assessed by enzyme-linked immunosorbent assay (ELISA).

RESULTS

The level of circRNA circ_0130438 was reduced in RA tissues (P = 0.0001) and FLSs isolated from RA tissues (P = 0.0001) compared with corresponding normal controls. Exposure of human fibroblast-like MH7A synoviocytes to TNF-α suppressed circRNA circ_0130438 expression (P < 0.0001). In contrast, the elevated expression of circRNA circ_0130438 suppressed the TNF-α-induced proliferation (P = 0.0047) and migration (P = 0.0023) of MH7A cells, as well as their pro-inflammatory cytokines (IL-1β, IL-6 and IL-8) production (P < 0.0001, P < 0.0001 and P < 0.0001). The circRNA circ_0130438 contained a miR-130a-3p binding site. Furthermore, the increase of miR-130-3p in TNF-α-stimulated MH7A cells reversed the effects of circRNA circ_0130438 elevation on cell proliferation (P = 0.0006), migration (P = 0.0406) and pro-inflammatory cytokines (IL-1β, IL-6 and IL-8) production (P = 0.0036, P < 0.0001 and P = 0.0004), indicating that miR-130a-3p was a functional mediator of circRNA circ_0130438 regulation. We also documented that KLF9 was a direct target and downstream effector of miR-130a-3p. Importantly, circRNA circ_0130438 enhanced KLF9 expression (P < 0.0001) in TNF-α-stimulated MH7A cells by functioning as a competing endogenous RNA (ceRNA) for miR-130a-3p (P = 0.0004).

CONCLUSION

Our findings demonstrate that the elevated expression of circRNA circ_0130438 suppresses TNF-α-induced migration, proliferation and pro-inflammatory cytokines (IL-1β, IL-6 and IL-8) production of human MH7A cells by enhancing KLF9 expression by operating as a ceRNA for miR-130a-3p.

摘要

背景

环状 RNA(circRNAs)可通过与共享 microRNAs(miRNAs)竞争来调节基因表达,从而在类风湿关节炎(RA)发病机制中发挥关键作用,miRNAs 是一类小的非编码 RNA。miR-130a-3p 是一种与疾病相关的 miRNA,Kruppel 样因子 9(KLF9)是一种锌指转录因子,它们都参与了 RA 的发病机制。在这里,我们鉴定了 circRNA circ_0130438 在调节肿瘤坏死因子 α(TNF-α)刺激的成纤维样滑膜细胞(FLSs)中的作用。

方法

通过生物信息学分析预测 miR-130a-3p 与 circRNA circ_0130438 或 KLF9 之间的直接关系,并通过双荧光素酶报告或 RNA 免疫沉淀(RIP)实验进行验证。通过定量实时 PCR(qRT-PCR)或 Western blot 方法检测 circRNA circ_0130438、miR-130a-3p 和 KLF9 因子的表达水平。通过 5-乙炔基-2'-脱氧尿苷(EdU)染色实验分析细胞增殖能力。Transwell 实验用于评估细胞迁移和侵袭能力。通过酶联免疫吸附试验(ELISA)评估白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和白细胞介素-8(IL-8)的产生水平。

结果

与相应的正常对照相比,RA 组织(P=0.0001)和 RA 组织分离的 FLSs 中 circRNA circ_0130438 的水平降低(P=0.0001)。TNF-α暴露于人成纤维样 MH7A 滑膜细胞中抑制 circRNA circ_0130438 的表达(P<0.0001)。相比之下,circRNA circ_0130438 的表达升高抑制了 TNF-α诱导的 MH7A 细胞的增殖(P=0.0047)和迁移(P=0.0023),以及它们的促炎细胞因子(IL-1β、IL-6 和 IL-8)的产生(P<0.0001、P<0.0001 和 P<0.0001)。circRNA circ_0130438 包含一个 miR-130a-3p 结合位点。此外,TNF-α刺激的 MH7A 细胞中 miR-130a-3p 的增加逆转了 circRNA circ_0130438 升高对细胞增殖(P=0.0006)、迁移(P=0.0406)和促炎细胞因子(IL-1β、IL-6 和 IL-8)产生(P=0.0036、P<0.0001 和 P=0.0004)的影响,表明 miR-130a-3p 是 circRNA circ_0130438 调节的功能介质。我们还记录到 KLF9 是 miR-130a-3p 的直接靶标和下游效应子。重要的是,circRNA circ_0130438 通过作为 miR-130a-3p 的竞争性内源 RNA(ceRNA)增强了 TNF-α刺激的 MH7A 细胞中 KLF9 的表达(P<0.0001)(P=0.0004)。

结论

我们的研究结果表明,circRNA circ_0130438 通过作为 miR-130a-3p 的 ceRNA 增强 KLF9 的表达,从而抑制 TNF-α诱导的人 MH7A 细胞的迁移、增殖和促炎细胞因子(IL-1β、IL-6 和 IL-8)的产生,从而抑制 TNF-α诱导的 MH7A 细胞的迁移、增殖和促炎细胞因子(IL-1β、IL-6 和 IL-8)的产生。

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