伤口愈合
PTEN公司
张力素
细胞生物学
PI3K/AKT/mTOR通路
生物
信号转导
细胞迁移
激酶
细胞
生物化学
免疫学
作者
Min Zhao,Bing Song,Jin Pu,Teiji Wada,Brian Reid,Guangping Tai,Fei Wang,Aihua Guo,Petr Walczysko,Yu Gu,Takehiko Sasaki,Akira Suzuki,John V. Forrester,Henry R. Bourne,Peter N. Devreotes,Colin McCaig,Josef Penninger
出处
期刊:Nature
[Springer Nature]
日期:2006-07-01
卷期号:442 (7101): 457-460
被引量:956
摘要
Wound healing is essential for maintaining the integrity of multicellular organisms. In every species studied, disruption of an epithelial layer instantaneously generates endogenous electric fields, which have been proposed to be important in wound healing. The identity of signalling pathways that guide both cell migration to electric cues and electric-field-induced wound healing have not been elucidated at a genetic level. Here we show that electric fields, of a strength equal to those detected endogenously, direct cell migration during wound healing as a prime directional cue. Manipulation of endogenous wound electric fields affects wound healing in vivo. Electric stimulation triggers activation of Src and inositol-phospholipid signalling, which polarizes in the direction of cell migration. Notably, genetic disruption of phosphatidylinositol-3-OH kinase-gamma (PI(3)Kgamma) decreases electric-field-induced signalling and abolishes directed movements of healing epithelium in response to electric signals. Deletion of the tumour suppressor phosphatase and tensin homolog (PTEN) enhances signalling and electrotactic responses. These data identify genes essential for electrical-signal-induced wound healing and show that PI(3)Kgamma and PTEN control electrotaxis.
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