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Interferon regulatory factor 6 regulates keratinocyte migration.
Biggs, Leah C; Naridze, Rachelle L; DeMali, Kris A; Lusche, Daniel F; Kuhl, Spencer; Soll, David R; Schutte, Brian C; Dunnwald, Martine.
Affiliation
  • Biggs LC; Department of Pediatrics, The University of Iowa, Iowa City, IA 52242, USA Interdisciplinary Graduate Program in Genetics, The University of Iowa, Iowa City, IA 52242, USA.
  • Naridze RL; Department of Pediatrics, The University of Iowa, Iowa City, IA 52242, USA.
  • DeMali KA; Department of Biochemistry, The University of Iowa, Iowa City, IA 52242, USA.
  • Lusche DF; Developmental Studies Hybridoma Bank, Department of Biology, The University of Iowa, Iowa City, IA 52242, USA.
  • Kuhl S; Developmental Studies Hybridoma Bank, Department of Biology, The University of Iowa, Iowa City, IA 52242, USA.
  • Soll DR; Developmental Studies Hybridoma Bank, Department of Biology, The University of Iowa, Iowa City, IA 52242, USA.
  • Schutte BC; Departments of Microbiology and Molecular Genetics and of Pediatrics and Human Development, Michigan State University, East Lansing, MI 48824, USA.
  • Dunnwald M; Department of Pediatrics, The University of Iowa, Iowa City, IA 52242, USA Interdisciplinary Graduate Program in Genetics, The University of Iowa, Iowa City, IA 52242, USA martine-dunnwald@uiowa.edu.
J Cell Sci ; 127(Pt 13): 2840-8, 2014 Jul 01.
Article in En | MEDLINE | ID: mdl-24777480
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Keratinocytes / Cell Movement / Interferon Regulatory Factors Limits: Animals / Pregnancy Language: En Journal: J Cell Sci Year: 2014 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Keratinocytes / Cell Movement / Interferon Regulatory Factors Limits: Animals / Pregnancy Language: En Journal: J Cell Sci Year: 2014 Document type: Article Affiliation country: United States Country of publication: United kingdom