SMAD公司
瘢痕疙瘩
Smad2蛋白
化学
磷酸化
生长分化因子-9
MAPK/ERK通路
转化生长因子
疤痕
癌症研究
发病机制
细胞生物学
信号转导
内科学
生物化学
医学
生物
病理
基因
胚胎发生
卵泡发生
作者
Xin Wu,Difei Bian,Yannong Dou,Zhunan Gong,Qian Tan,Yufeng Xia,Yue Dai
摘要
Abstract 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.
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