miR-146b破坏表皮生长因子受体/转化生长因子β受体前纤维化前馈回路,抑制肺成纤维细胞增殖和分化。

IF 3.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Yan Xie, Yapei Huang, Venkatlaxmi Chettiar, Tianzhou Xing, Steven K Huang, Bethany B Moore, Hiroshi Asahara, Peter W Abel, Yaping Tu
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引用次数: 0

摘要

特发性肺纤维化(IPF)是一种进行性且经常致命的肺部疾病。尽管最近治疗取得了进展,但IPF患者的存活率仍然很低,这反映了对疾病机制有更深入了解的迫切需要。IPF进展的一个关键特征是成纤维细胞的过度生长和向肌成纤维细胞的转化,这是由一个涉及转化生长因子(TGF) α和β1等介质的促纤维化前反馈回路驱动的。这些因子激活表皮生长因子受体(EGFR)和TGFβ1受体(TGFβR1),使纤维化永久化。microrna在调节基因表达中起着至关重要的作用,许多microrna在IPF中被破坏。通过RNA测序和定量逆转录聚合酶链反应,我们发现在TGFβ1治疗后,miR-146b是人肺成纤维细胞(HLF)中表达减少最显著的mirna之一,其表达减少了70%。尽管miR-146b通常在肺成纤维细胞中含量丰富,但其在来自IPF患者(HLF-F)和实验性肺纤维化小鼠的肺成纤维细胞中的水平明显较低。与非纤维化成纤维细胞相比,HLF-F对纤维化信号表现出更大的反应。升高HLF-F中miR-146b水平可降低tgf α-诱导的增殖,抑制tgf β1诱导的肌成纤维细胞分化60%-90%。相反,miR-146b基因的缺失增强了小鼠肺成纤维细胞的纤维化反应。此外,miR-146b直接靶向关键信号通路,包括EGFR、Jun、TGFβR1和SMAD3,从而抑制成纤维细胞增殖和成纤维活性。因此,靶向miR-146b是一种很有前景的治疗策略,通过调节EGFR和TGFβR信号通路的促纤维化前馈环来抑制肺成纤维细胞的增殖和分化。意义声明:对促纤维化介质的反应,过度成纤维细胞增殖和分化为肌成纤维细胞被认为是特发性肺纤维化进展的关键步骤。本研究通过抑制肺成纤维细胞增殖和分化,发现miR-146b是一种重要的内源性抗纤维化因子。转化生长因子β1对miR-146b的抑制也揭示了特发性肺纤维化中驱动纤维化和细胞过度生长的因素之间的新机制,为通过恢复miR-146b表达来减缓疾病进展和改善患者预后开辟了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
miR-146b disrupts the epidermal growth factor receptor/transforming growth factor β receptor profibrotic feedforward loop to inhibit lung fibroblast proliferation and differentiation.

Idiopathic pulmonary fibrosis (IPF) is a progressive and often fatal lung disease. Despite recent treatment advancements, survival rates for IPF patients remain low, reflecting the urgent need for a deeper understanding of disease mechanisms. A key feature of IPF progression is the excessive growth of fibroblasts and their transformation into myofibroblasts, driven by a profibrotic feedforward loop involving mediators like transforming growth factor (TGF) α and β1. These factors activate the epidermal growth factor receptor (EGFR) and TGFβ1 receptor (TGFβR1), perpetuating fibrosis. MicroRNAs play a vital role in regulating gene expression, and many are disrupted in IPF. Through RNA sequencing and quantitative reverse-transcription polymerase chain reaction, we identified miR-146b as one of the most significantly reduced miRNAs in human lung fibroblasts (HLF) following TGFβ1 treatment, with a confirmed 70% decrease in expression. Although miR-146b is normally abundant in lung fibroblasts, its levels are significantly lower in lung fibroblasts from IPF patients (HLF-F) and in mice with experimental pulmonary fibrosis. HLF-F exhibited greater responses to profibrotic signals compared with nonfibrotic fibroblasts. Elevating miR-146b levels in HLF-F reduced TGFα-induced proliferation and inhibited TGFβ1-induced myofibroblast differentiation by 60%-90%. Conversely, deletion of the miR-146b gene enhanced fibrotic responses in mouse lung fibroblasts. Additionally, miR-146b directly targets critical signaling pathways, including EGFR, Jun, TGFβR1, and SMAD3, thereby suppressing fibroblast proliferative and fibrogenic activities. Thus, targeting miR-146b presents a promising therapeutic strategy to inhibit lung fibroblast proliferation and differentiation by modulating the profibrotic feedforward loop of EGFR and TGFβR signaling pathways. SIGNIFICANCE STATEMENT: Excess fibroblast proliferation and differentiation into myofibroblasts in response to profibrotic mediators are considered key steps in idiopathic pulmonary fibrosis progression. This study identified miR-146b as an important endogenous antifibrotic factor via inhibition of both lung fibroblast proliferation and differentiation. The repression of miR-146b by transforming growth factor β1 also uncovers a new mechanism linking the factors that drive fibrosis and excessive cell growth in idiopathic pulmonary fibrosis, opening up new avenues for slowing disease progression and improving patient outcomes via restoration of miR-146b expression.

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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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