Bcl-3 acts as an innate immune modulator by controlling antimicrobial responses in keratinocytes

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Abstract

Innate immune responses involve the production of antimicrobial peptides (AMPs), chemokines, and cytokines. We report here the identification of B-cell leukemia (Bcl)-3 as a modulator of innate immune signaling in keratinocytes. In this study, it is shown that Bcl-3 is inducible by the Th2 cytokines IL-4 and IL-13 and is overexpressed in lesional skin of atopic dermatitis (AD) patients. Bcl-3 was shown to be important to cutaneous innate immune responses as silencing of Bcl-3 by small-interfering RNA (siRNA) reversed the downregulatory effect of IL-4 on the HBD3 expression. Bcl-3 silencing enhanced vitamin D3 (1,25D3)-induced gene expression of cathelicidin AMP in keratinocytes, suggesting a negative regulatory function on cathelicidin transcription. Furthermore, 1,25D3 suppressed Bcl-3 expression in vitro and in vivo. This study identified Bcl-3 as an important modulator of cutaneous innate immune responses and its possible therapeutic role in AD. © 2009 The Society for Investigative Dermatology.

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Büchau, A. S., MacLeod, D. T., Morizane, S., Kotol, P. F., Hata, T., & Gallo, R. L. (2009). Bcl-3 acts as an innate immune modulator by controlling antimicrobial responses in keratinocytes. Journal of Investigative Dermatology, 129(9), 2148–2155. https://doi.org/10.1038/jid.2009.49

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