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碱性成纤维细胞生长因子通过激活PI3K/Akt-Rac1-FAK-JNK和ERK信号通路促进黑素细胞迁移。

Basic fibroblast growth factor promotes melanocyte migration via activating PI3K/Akt-Rac1-FAK-JNK and ERK signaling pathways.

作者信息

Shi Hongxue, Lin Beibei, Huang Yan, Wu Jiang, Zhang Hongyu, Lin Cai, Wang Zhouguang, Zhu Jingjing, Zhao Yingzhen, Fu Xiaobing, Lou Zhencai, Li Xiaokun, Xiao Jian

机构信息

School of Pharmaceutical Sciences, Key Laboratory of Biotechnology and Pharmaceutical Engineering, Wenzhou Medical University, Wenzhou, China.

Wound Healing and Cell Biology Laboratory, Institute of Basic Medical Science, Chinese PLA General Hospital, Beijing, China.

出版信息

IUBMB Life. 2016 Sep;68(9):735-47. doi: 10.1002/iub.1531. Epub 2016 Jun 27.

Abstract

Vitiligo is a depigmentation disorder characterized by loss of functional melanocytes of the skin epidermis. The pathogenesis of vitiligo remains elusive. The purpose of this study is to investigate the effects of basic fibroblast growth factor (bFGF) on melanocyte migration, including its biochemical mechanism using transwell assay in vitro. We found that melanocyte treated with bFGF showed a significant increase in migration and cytoskeletal rearrangement. These changes were associated with increased activation of PI3K/Akt, Rac1, FAK, JNK, and ERK. Likewise, reduction of PI3K/Akt, Rac1, FAK, JNK, and ERK activity using selective inhibitors or siRNA was associated with impediment of bFGF-induced melanocyte migration. In addition, activity of Rac1, FAK, and JNK was reduced in cells in which PI3K/Akt was inhibited, activity of FAK and JNK was reduced in cells in which the Rac1 was inhibited, and activity of JNK was reduced in cells in which the FAK was inhibited. Collectively, these data demonstrate that bFGF facilitated melanocyte migration via PI3K/Akt-Rac1-FAK-JNK and ERK signaling pathways. © 2016 IUBMB Life, 68(9):735-747, 2016.

摘要

白癜风是一种色素脱失性疾病,其特征是皮肤表皮功能性黑素细胞丧失。白癜风的发病机制仍不清楚。本研究的目的是利用体外transwell试验研究碱性成纤维细胞生长因子(bFGF)对黑素细胞迁移的影响,包括其生化机制。我们发现,用bFGF处理的黑素细胞迁移和细胞骨架重排显著增加。这些变化与PI3K/Akt、Rac1、FAK、JNK和ERK的激活增加有关。同样,使用选择性抑制剂或小干扰RNA降低PI3K/Akt、Rac1、FAK、JNK和ERK的活性与bFGF诱导的黑素细胞迁移受阻有关。此外,在PI3K/Akt被抑制的细胞中,Rac1、FAK和JNK的活性降低;在Rac1被抑制的细胞中,FAK和JNK的活性降低;在FAK被抑制的细胞中,JNK的活性降低。总的来说,这些数据表明bFGF通过PI3K/Akt-Rac1-FAK-JNK和ERK信号通路促进黑素细胞迁移。©2016国际生物化学与分子生物学联盟生命科学部,68(9):735 - 747,2016。

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