在表达α-平滑肌肌动蛋白的细胞中消减LRP6,可在博莱霉素诱导的肺损伤后缓解肺部炎症和纤维化

Eun-Ah Sung, Mikhali G. Dozmorov, SuJeong Song, Theingi Aung, Min Hee Park, Patricia J. Sime, Wook-Jin Chae
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引用次数: 0

摘要

低密度脂蛋白受体相关蛋白 6(LRP6)是一种 Wnt 配体受体。组织纤维化是细胞外基质蛋白(ECM)过度沉积的渐进病理过程。通过α-平滑肌肌动蛋白(alphaSMA)表达确定的肌成纤维细胞通过产生 ECM 在组织纤维化中发挥着重要作用。在这里,我们发现 Wnt 拮抗剂 Dickkopf1(DKK1)可诱导肺成纤维细胞中与炎症和纤维化相关的基因表达。我们利用 Acta2-cre Lrp6 fl/fl(Lrp6 AKO)小鼠证明,在表达 alphaSMA 的细胞中遗传性缺失 LRP6 可消减博莱霉素(BLM)诱导的肺部炎症和纤维化表型,这表明 LRP6 在调节肺部炎症和纤维化过程中发挥着重要作用。我们的研究结果突显了成纤维细胞中的 LRP6 在 BLM 诱导的肺损伤中调节炎症和纤维化的关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ablation of LRP6 in alpha-smooth muscle actin-expressing cells abrogates lung inflammation and fibrosis upon bleomycin-induced lung injury
Low-density lipoprotein receptor-related protein 6 (LRP6) is a receptor for Wnt ligands. Tissue fibrosis is a progressive pathological process with excessive extracellular matrix proteins (ECM) deposition. Myofibroblasts, identified by alpha-smooth muscle actin (alphaSMA) expression, play an important role in tissue fibrosis by producing ECM production. Here we found that Wnt antagonist Dickkopf1 (DKK1) induced gene expressions associated with inflammation and fibrosis in lung fibroblasts. We demonstrated that genetic deletion of LRP6 in alphaSMA-expressing cells using Acta2-cre Lrp6 fl/fl (Lrp6 AKO) mice abrogated bleomycin (BLM)-induced lung inflammation and fibrosis phenotype, suggesting an important role of LRP6 in modulating inflammation and fibrotic processes in the lung. Our results highlight the crucial role of LRP6 in fibroblasts in regulating inflammation and fibrosis upon BLM-induced lung injury.
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