| Literature DB >> 21316034 |
Yuka Hiroshima1, Mika Bando, Masatoshi Kataoka, Yuji Inagaki, Mark C Herzberg, Karen F Ross, Kazuo Hosoi, Toshihiko Nagata, Jun-Ichi Kido.
Abstract
In the oral cavity, mucosal keratinocytes resist bacterial infection, in part, by producing broad-spectrum antimicrobial peptides (AMPs) including defensin, adrenomedullin and calprotectin. Epidermal keratinocyte expression of many AMPs increases in response to interleukin-1α (IL-1α). IL-1α is produced by epidermal keratinocytes and regulates cell differentiation. To better understand innate immunity in the oral cavity, we sought to determine how IL-1α might regulate expression of AMPs by human gingival keratinocytes (HGKs) using DNA microarray and Western blot analyses. HGKs from three subjects expressed eleven AMPs, including S100A7, S100A8, S100A9, S100A12, secretory leucocyte protease inhibitor, lipocalin 2 (LCN2), cystatin C and β-defensin 2. Of the expressed AMPs, S100A7, S100A12 and LCN2 were up-regulated by IL-1α (inducible AMPs); the other AMPs were considered to be constitutive. Human gingival keratinocytes, therefore, express constitutive and IL-1α-inducible AMPs to provide a rapid and robust innate response to microbial infection.Entities:
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Year: 2011 PMID: 21316034 PMCID: PMC3412402 DOI: 10.1016/j.archoralbio.2011.01.004
Source DB: PubMed Journal: Arch Oral Biol ISSN: 0003-9969 Impact factor: 2.633