Zhao Danyang, Wang Yu, Du Chao, Shan Shengzhou, Zhang Yifan, Du Zijing, Han Dong
Department of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of MedicineShanghai, China.
Department of Geriatrics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of MedicineShanghai, China.
Front Pharmacol. 2017 Apr 19;8:206. doi: 10.3389/fphar.2017.00206. eCollection 2017.
Hypertrophic scar (HPS) presents as excessive extracellular matrix deposition and abnormal function of fibroblasts. However, there is no single satisfactory method to prevent HPS formation so far. Here, we found that honokiol (HKL), a natural compound isolated from Magnolia tree, had an inhibitory effect on HPS both and . Firstly, HKL could dose-dependently down-regulate the mRNA and protein levels of type I collagen, type III collagen, and α-smooth muscle actin (α-SMA) in hypertrophic scar-derived fibroblasts (HSFs). Secondly, HKL suppressed the proliferation, migration abilities of HSFs and inhibited HSFs activation to myofibroblasts, but had no effect on cell apoptosis. Besides, the rabbit ear scar model further affirmed the inhibitory effects of HKL on collagen deposition, proliferating cell nuclear antigen and α-SMA. Finally, Western blot results showed that HKL reduced the phosphorylation status of Smad2/3, as well as affected the protein levels of matrix metalloproteinases (MMPs) and tissue inhibitor of metalloproteinase1. Taken together, this study demonstrated that HKL alleviated HPS by suppressing fibrosis-related molecules and inhibiting HSFs proliferation, migration as well as activation to myofibroblasts via Smad-dependent pathway. Therefore, HKL could be used as a potential agent for treating HPS and other fibrotic diseases.
肥厚性瘢痕(HPS)表现为细胞外基质过度沉积和成纤维细胞功能异常。然而,迄今为止尚无单一令人满意的方法来预防HPS形成。在此,我们发现从木兰树中分离出的天然化合物厚朴酚(HKL)对HPS在体内和体外均具有抑制作用。首先,HKL可剂量依赖性下调肥厚性瘢痕来源的成纤维细胞(HSFs)中I型胶原蛋白、III型胶原蛋白和α-平滑肌肌动蛋白(α-SMA)的mRNA和蛋白质水平。其次,HKL抑制HSFs的增殖、迁移能力,并抑制HSFs向肌成纤维细胞的活化,但对细胞凋亡无影响。此外,兔耳瘢痕模型进一步证实了HKL对胶原蛋白沉积、增殖细胞核抗原和α-SMA的抑制作用。最后,蛋白质印迹结果表明,HKL降低了Smad2/3的磷酸化状态,同时影响了基质金属蛋白酶(MMPs)和金属蛋白酶组织抑制剂1的蛋白质水平。综上所述,本研究表明HKL通过抑制纤维化相关分子,并通过Smad依赖途径抑制HSFs的增殖、迁移以及向肌成纤维细胞的活化来减轻HPS。因此,HKL可作为治疗HPS和其他纤维化疾病的潜在药物。