The neuroendocrine peptide catestatin is a cutaneous antimicrobial and induced in the skin after injury

被引:100
作者
Radek, Katherine A. [1 ,2 ]
Lopez-Garcia, Belen [1 ,2 ]
Hupe, Melanie [3 ,4 ]
Niesman, Ingrid R. [1 ]
Elias, Peter M. [3 ,4 ]
Taupenot, Laurent [1 ,2 ]
Mahata, Sushil K. [1 ,2 ]
O'Connor, Daniel T. [1 ,2 ,5 ]
Gallo, Richard L. [1 ,2 ]
机构
[1] Vet Affairs San Diego Healthcare Syst, Dept Dermatol, San Diego, CA 92161 USA
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[3] Univ Calif San Francisco, Sch Med, Dept Dermatol, San Francisco, CA 94143 USA
[4] Vet Adm Med Ctr, Dept Dermatol, San Francisco, CA 94121 USA
[5] Univ Calif San Diego, Ctr Mol Genet, Dept Med & Pharmacol, La Jolla, CA 92093 USA
关键词
D O I
10.1038/sj.jid.5701225
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Epithelia establish a microbial barrier against infection through the production of antimicrobial peptides ( AMPs). In this study, we investigated whether catestatin ( Cst), a peptide derived from the neuroendocrine protein chromogranin A (CHGA), is a functional AMP and is present in the epidermis. We show that Cst is antimicrobial against relevant skin microbes, including Gram-positive and Gram-negative bacteria, yeast, and fungi. The antimicrobial mechanism of Cst was found to be similar to other AMPs, as it was dependent on bacterial charge and growth conditions, and induced membrane disruption. The potential relevance of Cst against skin pathogens was supported by the observation that CHGA was expressed in keratinocytes. In human skin, CHGA was found to be proteolytically processed into the antimicrobial fragment Cst, thus enabling its AMP function. Furthermore, Cst expression in murine skin increased in response to injury and infection, providing potential for increased protection against infection. These data demonstrate that a neuroendocrine peptide has antimicrobial function against a wide assortment of skin pathogens and is upregulated upon injury, thus demonstrating a direct link between the neuroendocrine and cutaneous immune systems.
引用
收藏
页码:1525 / 1534
页数:10
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