Faculté de Médecine, CNRS, Inserm, iBV, Université Côte d'Azur, 06107 Nice, France.
FHU-OncoAge, CNRS, IPMC, Université Côte d'Azur, 06560 Valbonne, France.
Cells. 2021 Jul 20;10(7):1832. doi: 10.3390/cells10071832.
Fibrosis is a deleterious invasion of tissues associated with many pathological conditions, such as Duchenne muscular dystrophy (DMD) for which no cure is at present available for its prevention or its treatment. Fibro-adipogenic progenitors (FAPs) are resident cells in the human skeletal muscle and can differentiate into myofibroblasts, which represent the key cell population responsible for fibrosis. In this study, we delineated the pool of microRNAs (miRNAs) that are specifically modulated by TGFβ1 in FAPs versus myogenic progenitors (MPs) by a global miRNome analysis. A subset of candidates, including several "FibromiRs", was found differentially expressed between FAPs and MPs and was also deregulated in DMD versus healthy biopsies. Among them, the expression of the TGFβ1-induced miR-199a~214 cluster was strongly correlated with the fibrotic score in DMD biopsies. Loss-of-function experiments in FAPs indicated that a miR-214-3p inhibitor efficiently blocked expression of fibrogenic markers in both basal conditions and following TGFβ1 stimulation. We found that FGFR1 is a functional target of miR-214-3p, preventing the signaling of the anti-fibrotic FGF2 pathway during FAP fibrogenesis. Overall, our work demonstrates that the « FibromiR » miR-214-3p is a key activator of FAP fibrogenesis by modulating the FGF2/FGFR1/TGFβ axis, opening new avenues for the treatment of DMD.
纤维化是一种与许多病理状况相关的组织破坏性浸润,例如杜氏肌营养不良症(DMD),目前尚无针对其预防或治疗的方法。纤维脂肪祖细胞(FAPs)是人体骨骼肌中的固有细胞,可分化为肌成纤维细胞,后者是导致纤维化的关键细胞群体。在这项研究中,我们通过全局 miRNA 组分析描绘了 TGFβ1 在 FAPs 与肌原性祖细胞(MPs)中特异性调节的 miRNA 池。一组候选 miRNA,包括几个“Fibromirs”,在 FAPs 和 MPs 之间差异表达,在 DMD 与健康活检之间也失调。其中,TGFβ1 诱导的 miR-199a~214 簇的表达与 DMD 活检中的纤维化评分强烈相关。在 FAPs 中进行的功能丧失实验表明,miR-214-3p 的抑制剂在基础条件下和 TGFβ1 刺激后都能有效地阻断纤维生成标志物的表达。我们发现 FGFR1 是 miR-214-3p 的功能性靶标,可防止 FAP 纤维化过程中抗纤维化 FGF2 途径的信号传导。总的来说,我们的工作表明,“Fibromir”miR-214-3p 通过调节 FGF2/FGFR1/TGFβ 轴成为 FAP 纤维化的关键激活因子,为 DMD 的治疗开辟了新途径。