Literature DB >> 15829297

Correlation between beta-defensin expression and induction profiles in gingival keratinocytes.

Sophie Joly1, Connie C Organ, Georgia K Johnson, Paul B McCray, Janet M Guthmiller.   

Abstract

Human beta-defensins are antimicrobial peptides produced by epithelial cells. To date, 28 beta-defensins have been described and the expression of a select few has been classified as constitutive or inducible. Most studies have evaluated expression and regulation using a limited number of primary cell cultures or immortalized cell lines. The goal of this study was to quantitatively assess the in vitro expression and inducibility profiles of human beta-defensins, HBD-1, HBD-2, and HBD-3 across a number of primary gingival keratinocyte cultures. Cultured cells from 14 human subjects were stimulated with interleukin-1 beta (IL-1beta), IL-2, IL-6, IL-8, IL-12, tumor necrosis factor alpha (TNF-alpha), gamma interferon (IFN-gamma) or Escherichia coli lipopolysaccharide (LPS) and analyzed by reverse transcription (RT)-PCR. A subset of cultures were quantitatively assessed by real-time PCR. HBD-1 presented the highest and most heterogeneous expression at the basal level (non-stimulated) as compared to expression of HBD-2 and HBD-3, which was significantly lower and homogeneous. IFN-gamma was a primary inducer for HBD-1 and HBD-3, while IL-1beta and TNF-alpha were primary inducers for HBD-2. Sporadic induction was seen for IL-2, IL-6 and LPS. Synergistic expression was seen when various cytokines were combined. Interestingly, the induction potential of each beta-defensin was directly correlated to its basal expression. An inhibitor of JAK2 kinase (Janus kinase), down-regulated IFN-gamma-induced HBD-1 and HBD-3 expression, suggesting a role for the JAK/signal transducer and activator of transcription (STAT) signaling pathway in their expression. HBD-2 protein expression of supernatants and cell lysates paralleled mRNA expression. The results suggest that beta-defensin expression and induction in gingival keratinocytes is similar to that seen in other tissue. However, the novel finding of considerable variation among induction levels and the correlation of the induction with basal expression suggests that these innate response elements may play a key role in susceptibility or resistance to disease in the oral cavity.

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Year:  2004        PMID: 15829297     DOI: 10.1016/j.molimm.2004.11.001

Source DB:  PubMed          Journal:  Mol Immunol        ISSN: 0161-5890            Impact factor:   4.407


  44 in total

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2.  Capacity of human beta-defensin expression in gene-transduced and cytokine-induced cells.

Authors:  Chunyi Yin; Hoa N Dang; Hai-Bo Zhang; Farzad Gazor; Daniel Kim; Ole E Sorensen; George T-J Huang
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Review 3.  Host defense peptides in wound healing.

Authors:  Lars Steinstraesser; Till Koehler; Frank Jacobsen; Adrien Daigeler; Ole Goertz; Stefan Langer; Marco Kesting; Hans Steinau; Elof Eriksson; Tobias Hirsch
Journal:  Mol Med       Date:  2008 Jul-Aug       Impact factor: 6.354

4.  Differential cytotoxicity of long-chain bases for human oral gingival epithelial keratinocytes, oral fibroblasts, and dendritic cells.

Authors:  Christopher Poulsen; Leslie A Mehalick; Carol L Fischer; Emily A Lanzel; Amber M Bates; Katherine S Walters; Joseph E Cavanaugh; Janet M Guthmiller; Georgia K Johnson; Philip W Wertz; Kim A Brogden
Journal:  Toxicol Lett       Date:  2015-05-21       Impact factor: 4.372

5.  Human alpha- and beta-defensins bind to immobilized adhesins from Porphyromonas gingivalis.

Authors:  Deborah E Dietrich; Xiangjun Xiao; Deborah V Dawson; Myriam Bélanger; Hua Xie; Ann Progulske-Fox; Kim A Brogden
Journal:  Infect Immun       Date:  2008-10-13       Impact factor: 3.441

6.  Effect of growth factors on antimicrobial peptides and pro-inflammatory mediators during wound healing.

Authors:  H Dommisch; J Winter; W Götz; J Miesen; A Klein; L Hierse; J Deschner; A Jäger; J Eberhard; S Jepsen
Journal:  Clin Oral Investig       Date:  2014-05-07       Impact factor: 3.573

7.  Normal human gingival epithelial cells sense C. parapsilosis by toll-like receptors and module its pathogenesis through antimicrobial peptides and proinflammatory cytokines.

Authors:  Raouf Bahri; Sèverine Curt; Dalila Saidane-Mosbahi; Mahmoud Rouabhia
Journal:  Mediators Inflamm       Date:  2010-05-03       Impact factor: 4.711

8.  Dysregulation of human beta-defensin-2 protein in inflammatory bowel disease.

Authors:  Marian C Aldhous; Colin L Noble; Jack Satsangi
Journal:  PLoS One       Date:  2009-07-20       Impact factor: 3.240

9.  Association of a genetic polymorphism (-44 C/G SNP) in the human DEFB1 gene with expression and inducibility of multiple beta-defensins in gingival keratinocytes.

Authors:  Andrea A Kalus; L Page Fredericks; Beth M Hacker; Henrik Dommisch; Richard B Presland; Janet R Kimball; Beverly A Dale
Journal:  BMC Oral Health       Date:  2009-08-27       Impact factor: 2.757

10.  The expression of the beta-defensins hBD-2 and hBD-3 is differentially regulated by NF-kappaB and MAPK/AP-1 pathways in an in vitro model of Candida esophagitis.

Authors:  Nadine Steubesand; Karlheinz Kiehne; Gabriele Brunke; Rene Pahl; Karina Reiss; Karl-Heinz Herzig; Sabine Schubert; Stefan Schreiber; Ulrich R Fölsch; Philip Rosenstiel; Alexander Arlt
Journal:  BMC Immunol       Date:  2009-06-12       Impact factor: 3.615

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