In this issue, Takekoshi et al. investigated the role of CXCR4 in IL-23-induced keratinocyte hyperproliferation using an epidermal-specific knockout mouse model and found that CXCR4 limited keratinocyte proliferation. Some reports in the literature support this idea, whereas others contradict it; this disparity may be related to the differential roles of CXCR4 in various cell types or to a recently identified second receptor (CXCR7). Nevertheless, CXCR4 and its ligand SDF-1 have been implicated in skin wound healing, systemic lupus erythematosus, and basal cell carcinoma tumor angiogenesis. Further study is merited. © 2013 The Society for Investigative Dermatology.
CITATION STYLE
Bollag, W. B., & Hill, W. D. (2013). CXCR4 in epidermal keratinocytes: Crosstalk within the skin. Journal of Investigative Dermatology. Nature Publishing Group. https://doi.org/10.1038/jid.2013.271
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