Expression of MHC Class II, CD70, CD80, CD86 and pro-inflammatory cytokines is differentially regulated in oral epithelial cells following bacterial challenge

Authors

  • D. C. Han,

    1. The Jane and Jerry Weintraub Center for Reconstructive Biotechnology,
    2. Section of Endodontics, Division of Associated Clinical Specialties,
    3. Dental Research Institute, and the
    4. Division of Oral Biology and Oral Medicine. UCLA School of Medicine and Dentistry, Los Angeles, CA, USA
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  • G. T-J. Huang,

    1. Section of Endodontics, Division of Associated Clinical Specialties,
    2. Dental Research Institute, and the
    3. Division of Oral Biology and Oral Medicine. UCLA School of Medicine and Dentistry, Los Angeles, CA, USA
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  • L. M. Lin,

    1. Section of Endodontics, Division of Associated Clinical Specialties,
    2. Dental Research Institute, and the
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  • N. A. Warner,

    1. The Jane and Jerry Weintraub Center for Reconstructive Biotechnology,
    2. Section of Endodontics, Division of Associated Clinical Specialties,
    3. Dental Research Institute, and the
    4. Division of Oral Biology and Oral Medicine. UCLA School of Medicine and Dentistry, Los Angeles, CA, USA
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  • J. S. Gim,

    1. The Jane and Jerry Weintraub Center for Reconstructive Biotechnology,
    2. Dental Research Institute, and the
    3. Division of Oral Biology and Oral Medicine. UCLA School of Medicine and Dentistry, Los Angeles, CA, USA
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  • A. Jewett

    1. The Jane and Jerry Weintraub Center for Reconstructive Biotechnology,
    2. Dental Research Institute, and the
    3. Division of Oral Biology and Oral Medicine. UCLA School of Medicine and Dentistry, Los Angeles, CA, USA
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Anahid Jewett, Division of Oral Biology and Oral Medicine. UCLA School of Medicine and Dentistry, Los Angeles, CA 90095, USA
Tel.: +1 310 206 3970; fax: +1 310 794 7109;
e-mail: ajewett@ucla.edu

Abstract

Oral epithelium may play a regulatory role in local immune responses when interacting with bacteria. The present study was undertaken to investigate the effects of selected bacterial pathogens found in periodontal and endodontic infections on oral epithelial cells. Expression of cell surface molecules (major histocompatibility complex (MHC) Class II, CD54, CD70, CD80 and CD86) and secretion of inflammatory cytokines (interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α) in response to selected bacterial challenge were examined on an immortalized oral epithelial cell line, HOK-18A and a skin epithelial cell line, HaCaT. Actinomyces viscosus, Actinomyces israelii, Fusobacterium nucleatum lipopolysaccharide (LPS) or primary human periradicular exudate from a granuloma were co-cultured with epithelial cells for 4 or 24 h. Subsequently, cell surface expression of MHC Class II, CD54, CD70, CD80 and CD86, along with pro-inflammatory cytokine levels were determined using flow cytometry, ELISA and RT-PCR. Results indicated that the selected oral bacteria have greater effects on oral versus skin epithelial cells. F. nucleatum increased MHC Class II and CD54 (ICAM-1) cell surface expression on HOK-18A and HaCaT cells. A. israelii also had enhancing effects on the expression of CD54 and MHC Class II. A. israelii and LPS induced a 2.8-fold (P < 0.001) and 4.4-fold (P < 0.005) TNF-α secretion, respectively, while F. nucleatum and LPS induced a 10-fold (P < 0.0004) and 6-fold (P < 0.01) IL-1β secretion, respectively by HOK-18A. Interestingly, CD70, CD80, and CD86 were generally decreased upon bacteria and LPS challenge on HOK-18A. The effects of increased MHC Class II and decreased CD70 were also evident with challenge of human periradicular exudate on HOK-18A. The implications of the study are unique in that oral epithelial cells may play both activating and inhibitory roles in the host immune response towards infection by oral bacteria. We introduce a concept of ‘dormancy’ where the differential expression of key cell surface antigens on oral epithelial cells may keep the recruited immune effector cells in a state of unresponsiveness, thus contributing to the long term quiescent period observed in many periodontal and endodontic lesions.

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