Delayed skin wound repair in proline-rich protein tyrosine kinase 2 knockout mice

Aaron C. Koppel, Alexi Kiss, Anna Hindes, Carole J. Burns, Barry L. Marmer, Gregory Goldberg, Miroslav Blumenberg, Tatiana Efimova*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

14 Scopus citations


Proline-rich protein tyrosine kinase 2 (Pyk2 is a member of the focal adhesion kinase family. We used Pyk2 knockout (Pyk2-KO mice to study the role of Pyk2 in cutaneous wound repair. We report that the rate of wound closure was delayed in Pyk2-KO compared with control mice. To examine whether impaired wound healing of Pyk2-KO mice was caused by a keratinocyte cell-autonomous defect, the capacities of primary keratinocytes from Pyk2-KO and wild-type (WT littermates to heal scratch wounds in vitro were compared. The rate of scratch wound repair was decreased in Pyk2-KO keratinocytes compared with WT cells. Moreover, cultured human epidermal keratinocytes overexpressing the dominant-negative mutant of Pyk2 failed to heal scratch wounds. Conversely, stimulation of Pyk2-dependent signaling via WT Pyk2 overexpression induced accelerated scratch wound closure and was associated with increased expression of matrix metalloproteinase (MMP-1, MMP-9, and MMP-10. The Pyk2-stimulated increase in the rate of scratch wound repair was abolished by coexpression of the dominant-negative mutant of PKCδ and by GM-6001, a broad-spectrum inhibitor of MMP activity. These results suggest that Pyk2 is essential for skin wound reepithelialization in vivo and in vitro and that it regulates epidermal keratinocyte migration via a pathway that requires PKCδ and MMP functions.

Original languageEnglish (US)
Pages (from-to)C899-C909
JournalAmerican Journal of Physiology - Cell Physiology
Issue number10
StatePublished - May 15 2014


  • Epidermis
  • Knockout mice
  • Nonreceptor tyrosine kinase
  • Proline-rich protein tyrosine kinase 2
  • Wound healing

ASJC Scopus subject areas

  • Physiology
  • Cell Biology


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