Department of Anesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, P.R. China; Department of Physiology and Cell Biology, The Ohio State University, Columbus, Ohio.
Department of Physiology and Cell Biology, The Ohio State University, Columbus, Ohio.
Transl Res. 2020 Sep;223:15-24. doi: 10.1016/j.trsl.2020.05.004. Epub 2020 May 17.
Smad4 plays a central role in the regulation of extracellular matrix (ECM) protein expression and cell differentiation; however, the molecular regulation of Smad4 protein stability by a deubiquitinase has not been reported. In the current study, we reveal that a deubiquitinase USP13 stabilizes Smad4, ultimately modulating ECM protein expression in lung fibroblast cells. USP13 was increased in primary adult lung fibroblasts isolated from bleomycin-challenged mice and transforming growth factor (TGF)-β1-treated primary mouse lung fibroblasts. In a bleomycin-induced murine model of lung fibrosis, USP13-deficient mice showed reduced ECM levels such as fibronectin (FN) and collagen compared with wild-type mice. The reductions in both protein levels and mRNA expression of ECM were observed in the isolated lung fibroblasts from USP13-deficient mice, suggesting that downregulation of USP13 reduces ECM levels through inhibiting its transcription. To investigate the molecular mechanisms by which USP13 modulates ECM expression, we focused on the role of USP13 on Smad4 expression. Overexpression of USP13 increased FN and Smad4 protein levels in lung fibroblasts, while downregulation of USP13 reduced Smad4 protein levels, without altering Smad4 mRNA expression, suggesting that USP13 regulates Smad4 protein stability. Knockdown of USP13 decreased Smad4 half-life and promoted Smad4 ubiquitination. Both Smad4 and USP13 were co-localized in the cytoplasm in treated cell, and co-translocated into the nucleus in response to TGF-β1. The results indicate that USP13 promotes ECM expression by stabilizing Smad4 in lung fibroblasts and plays a role in the maintenance of the extracellular matrix in lungs.
Smad4 在细胞外基质(ECM)蛋白表达和细胞分化的调节中发挥核心作用;然而,去泛素化酶对 Smad4 蛋白稳定性的分子调控尚未报道。在本研究中,我们揭示了去泛素酶 USP13 稳定 Smad4,最终调节肺成纤维细胞中 ECM 蛋白的表达。USP13 在博莱霉素刺激的小鼠原代成纤维细胞和转化生长因子(TGF)-β1 处理的原代小鼠肺成纤维细胞中增加。在博莱霉素诱导的肺纤维化小鼠模型中,与野生型小鼠相比,USP13 缺陷小鼠的 ECM 水平(如纤维连接蛋白[FN]和胶原蛋白)降低。USP13 缺陷型小鼠分离的肺成纤维细胞中 ECM 的蛋白水平和 mRNA 表达均降低,表明 USP13 的下调通过抑制其转录降低 ECM 水平。为了研究 USP13 调节 ECM 表达的分子机制,我们重点研究了 USP13 对 Smad4 表达的作用。USP13 的过表达增加了肺成纤维细胞中 FN 和 Smad4 的蛋白水平,而 USP13 的下调降低了 Smad4 的蛋白水平,而不改变 Smad4 的 mRNA 表达,表明 USP13 调节 Smad4 蛋白的稳定性。USP13 的敲低降低了 Smad4 的半衰期并促进了 Smad4 的泛素化。在处理的细胞中,Smad4 和 USP13 都在细胞质中共定位,并在 TGF-β1 作用下共转位到细胞核。结果表明,USP13 通过稳定肺成纤维细胞中的 Smad4 促进 ECM 表达,并在维持肺部细胞外基质中发挥作用。