Wu Xin, Bian Difei, Dou Yannong, Gong Zhunan, Tan Qian, Xia Yufeng, Dai Yue
Jiangsu Key Laboratory of Drug Discovery for Metabolic Diseases, Department of Pharmacology of Chinese Materia Medica, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
Center for New Drug Research & Development, College of Life Science, Nanjing Normal University, Nanjing, 210024, People's Republic of China.
J Biochem Mol Toxicol. 2017 Aug;31(8). doi: 10.1002/jbt.21922. Epub 2017 Mar 27.
Higher expression of growth differentiation factor-9 (GDF-9) in keloids compared with hypertrophic scars and normal skin tissues has been reported recently. The present study was performed to investigate the role of GDF-9 in keloid pathogenesis, and to elucidate its implication for asiaticoside in the keloid management. The data showed that GDF-9 could enhance the proliferation, migration, and invasion of keloid fibroblasts (KFs), while it only slightly elevated collagen expression, indicating that the effect of GDF-9 was opposite to that of TGF-β1. The bioactivity difference between GDF-9 and TGF-β1 could be explained by the different phosphorylated sites on the downstream Smad2/3. Moreover, asiaticoside could inhibit GDF-9-induced activation of MAPKs and Smad pathway in KFs. In conclusion, GDF-9 enhanced the invasive growth of KFs, which was achieved by phosphorylation of Smad 2/3 at the linker region through activation of MAPKs pathway. Asiaticoside hindered the invasive growth of KFs by inhibiting the GDF-9/MAPK/Smad pathway.
最近有报道称,与增生性瘢痕和正常皮肤组织相比,瘢痕疙瘩中生长分化因子9(GDF-9)的表达更高。本研究旨在探讨GDF-9在瘢痕疙瘩发病机制中的作用,并阐明其在瘢痕疙瘩治疗中对积雪草苷的意义。数据显示,GDF-9可增强瘢痕疙瘩成纤维细胞(KFs)的增殖、迁移和侵袭能力,而其对胶原蛋白表达的提升作用较小,这表明GDF-9的作用与转化生长因子-β1(TGF-β1)相反。GDF-9与TGF-β1之间的生物活性差异可通过下游Smad2/3上不同的磷酸化位点来解释。此外,积雪草苷可抑制GDF-9诱导的KFs中丝裂原活化蛋白激酶(MAPKs)和Smad信号通路的激活。总之,GDF-9通过激活MAPKs通路使Smad 2/3在连接区磷酸化,从而增强KFs的侵袭性生长。积雪草苷通过抑制GDF-9/MAPK/Smad信号通路来阻碍KFs的侵袭性生长。