Pruritus, also known as itch, is a sensation that causes a desire to scratch. Prolonged scratching exacerbates skin lesions in several skin diseases such as atopic dermatitis. Here, we identify the cystic fibrosis transmembrane conductance regulator (CFTR/Cftr), an integral membrane protein that mediates transepithelial chloride transport, as a determinant factor in mice for the susceptibility to several cutaneous symptoms during mite infestation. Mice that endogenously express dysfunctional Cftr (CftrΔF508/ΔF508) show significant increase of scratching behavior and skin fibrosis after mite exposure. These phenotypes were due to the increased expression of nerve growth factor (NGF) that augments the sensitization of peripheral nerve fibers. Moreover, protein gene product 9.5 (PGP9.5)-positive neurites were abundant in the epidermis of mite-infested CftrΔF508/ΔF508mice. Furthermore, mite-infested Cftr+/+mice orally administered with a chloride channel inhibitor glibenclamide had higher scratching count and increased level of NGF than vehicle-treated mice. Consistently, mite extract-exposed primary and transformed human keratinocytes, treated with CFTR inhibitor, had significantly higher level of NGF mRNA compared with vehicle-treated, mite extract-exposed cells. These results reveal that CFTR in keratinocytes plays a critical role for the regulation of peripheral nerve function and pruritus sensation, and suggest that CftrΔF508/ΔF508mice may serve as a novel mouse model that represents NGF-dependent generation of pruritus.

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Keywords CFTR, keratinocyte, mite, nerve growth factor, pruritus, scratching behavior
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Journal Laboratory Investigation
Hashimoto, Y, Shuto, T, Mizunoe, S, Tomita, A, Koga, T, Sato, T, … Kai, H. (2011). CFTR-deficiency renders mice highly susceptible to cutaneous symptoms during mite infestation. Laboratory Investigation, 91(4), 509–518. doi:10.1038/labinvest.2010.193