β-cryptoxanthin regulates bone resorption related-cytokine production in human periodontal ligament cells
β-cryptoxanthin regulates bone resorption related-cytokine production in human periodontal ligament cells
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DOI:
10.1016/j.archoralbio.2013.01.005
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发表时间:
2013-07-01
影响因子:
3
通讯作者:
Kanamura, Narisato
中科院分区:
文献类型:
--
作者:
Nishigaki, Masaru;Yamamoto, Toshiro;Kanamura, Narisato
Objective: E-cryptoxanthin (beta-cry) is a type of carotenoid found in certain fruits and vegetables. Although it has been shown that beta-cry inhibits alveolar bone resorption, the molecular mechanisms for this have not yet been clarified. In the present study, we investigated the effects of beta-cry on bone resorption related-cytokine production in human periodontal ligament (hPDL) cells.Design: hPDL cells were stimulated with beta-cry (1 x 10(-7) mol/l), mechanical stress (1 or 6 MPa), and P. gingivalis. The production of interleukin (IL)-1 beta, IL-6, IL-8, tumour necrosis factor (TNF)-alpha, osteoprotegerin (OPG), and receptor activator of nuclear factor kappa-B ligand (RANKL) were analyzed by RT-PCR and ELISA.Results: The production of IL-1 beta, IL-6, IL-8, and TNF-alpha was not induced in hPDL cells after stimulation with beta-cry, although these cytokines were produced after stimulation with P. gingivalis. On the other hand, IL-6 and 1L-8 were produced after exposure to 6 MPa of mechanical stress. The production of IL-6 and IL-8 was significantly decreased by the addition of beta-cry. Furthermore, beta-cry up-regulated the production of OPG, but not RANKL.Conclusion: beta-cry inhibited the production of IL-6 and IL-8 induced by mechanical stress and periodontopathogenic bacteria in hPDL cells. Moreover, beta-cry up-regulated OPG production. These results suggest that beta-cry may prevent bone resorption in periodontitis. (C) 2013 Elsevier Ltd. All rights reserved.