Interferon regulatory factor 6 regulates keratinocyte migration

被引:43
作者
Biggs, Leah C. [1 ,2 ]
Naridze, Rachelle L. [1 ]
DeMali, Kris A. [3 ]
Lusche, Daniel F. [4 ]
Kuhl, Spencer [4 ]
Soll, David R. [4 ]
Schutte, Brian C. [5 ,6 ]
Dunnwald, Martine [1 ,2 ]
机构
[1] Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
[2] Univ Iowa, Interdisciplinary Grad Program Genet, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Biochem, Iowa City, IA 52242 USA
[4] Univ Iowa, Dept Biol, Dev Studies Hybridoma Bank, Iowa City, IA 52242 USA
[5] Michigan State Univ, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USA
[6] Michigan State Univ, Dept Pediat & Human Dev, E Lansing, MI 48824 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Interferon regulatory factor 6; Migration; Keratinocytes; BINDING PROTEIN RHO; VENTRAL BODY-WALL; ACTIN POLYMERIZATION; CELL-ADHESION; STRESS FIBERS; SMALL GTPASES; CAUSE VAN; ROCK-I; IRF6; DIFFERENTIATION;
D O I
10.1242/jcs.139246
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Interferon regulatory factor 6 (Irf6) regulates keratinocyte proliferation and differentiation. In this study, we tested the hypothesis that Irf6 regulates cellular migration and adhesion. Irf6-deficient embryos at 10.5 days post-conception failed to close their wound compared with wild-type embryos. In vitro, Irf6-deficient murine embryonic keratinocytes were delayed in closing a scratch wound. Live imaging of the scratch showed deficient directional migration and reduced speed in cells lacking Irf6. To understand the underlying molecular mechanisms, cell-cell and cell-matrix adhesions were investigated. We show that wild-type and Irf6-deficient keratinocytes adhere similarly to all matrices after 60 min. However, Irf6-deficient keratinocytes were consistently larger and more spread, a phenotype that persisted during the scratch-healing process. Interestingly, Irf6-deficient keratinocytes exhibited an increased network of stress fibers and active RhoA compared with that observed in wild-type keratinocytes. Blocking ROCK, a downstream effector of RhoA, rescued the delay in closing scratch wounds. The expression of Arhgap29, a Rho GTPase-activating protein, was reduced in Irf6-deficient keratinocytes. Taken together, these data suggest that Irf6 functions through the RhoA pathway to regulate cellular migration.
引用
收藏
页码:2840 / 2848
页数:9
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