Abstract
Gammadelta T cell receptor-bearing dendritic epidermal T cells (DETCs) found in murine skin recognize antigen expressed by damaged or stressed keratinocytes. Activated DETCs produce keratinocyte growth factors (KGFs) and chemokines, raising the possibility that DETCs play a role in tissue repair. We performed wound healing studies and found defects in keratinocyte proliferation and tissue reepithelialization in the absence of wild-type DETCs. In vitro skin organ culture studies demonstrated that adding DETCs or recombinant KGF restored normal wound healing in gammadelta DETC-deficient skin. We propose that DETCs recognize antigen expressed by injured keratinocytes and produce factors that directly affect wound repair.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Cell Division
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Cytokines / biosynthesis
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Dendritic Cells / cytology
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Dendritic Cells / immunology
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Dendritic Cells / physiology*
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Fibroblast Growth Factor 10
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Fibroblast Growth Factor 7
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Fibroblast Growth Factors / biosynthesis*
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Fibroblast Growth Factors / genetics
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Fibroblast Growth Factors / metabolism
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Fibroblast Growth Factors / pharmacology
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Keratinocytes / physiology*
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Lymphocyte Activation
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Mice
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Mice, Inbred C57BL
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Mice, Transgenic
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Organ Culture Techniques
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RNA, Messenger / genetics
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RNA, Messenger / metabolism
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Receptors, Antigen, T-Cell, gamma-delta / analysis*
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Skin / injuries
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T-Lymphocyte Subsets / cytology
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T-Lymphocyte Subsets / immunology
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T-Lymphocyte Subsets / physiology*
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Wound Healing*
Substances
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Cytokines
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Fgf7 protein, mouse
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Fibroblast Growth Factor 10
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RNA, Messenger
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Receptors, Antigen, T-Cell, gamma-delta
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Fibroblast Growth Factor 7
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Fibroblast Growth Factors