Resolvin E1 regulates inflammation at the cellular and tissue level and restores tissue homeostasis in vivo

被引:334
作者
Hasturk, Hatice
Kantarci, Alpdogan
Goguet-Surmenian, Emilie
Blackwood, Amanda
Andry, Chris
Serhan, Charles N.
Van Dyke, Thomas E.
机构
[1] Boston Univ, Goldman Sch Dent Med, Dept Periodontol & Oral Biol, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Dept Pathol, Boston, MA 02118 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Dept Anesthesiol Perioperat & Pain Med, Ctr Expt Therapeut & Reperfus Injury, Boston, MA 02115 USA
关键词
D O I
10.4049/jimmunol.179.10.7021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Resolvin E1 (RvE1) is a potent proresolving mediator of inflammation derived from omega-3 eicosapentaenoic acid that acts locally to stop leukocyte recruitment and promote resolution. RvE1 displays potent counter-regulatory and tissue-protective actions in vitro and in vivo. Periodontal disease is a local inflammatory disease initiated by bacteria characterized by neutrophilmediated tissue injury followed by development of a chronic immune lesion. In this study, we report the treatment of established periodontitis using RvE1 as a monotherapy in rabbits compared with structurally related lipids PGE(2) and leukotriene B-4 center dot PGE(2) and leukotriene B-4 each enhanced development of periodontitis and worsened the severity of disease. Promotion of resolution of inflammation as a therapeutic target with RvE1 resulted in complete restoration of the local lesion, and reduction in the systemic inflammatory markers C-reactive protein and IL-1 beta. This report is the first to show that resolution of inflammation by a naturally occurring endogenous lipid mediator results in complete regeneration of pathologically lost tissues, including bone.
引用
收藏
页码:7021 / 7029
页数:9
相关论文
共 74 条
  • [41] Diabetic periodontitis: a model for activated innate immunity and impaired resolution of inflammation
    Nassar, Hamdy
    Kantarci, Alpdogan
    Van Dyke, Thomas E.
    [J]. PERIODONTOLOGY 2000, 2007, 43 : 233 - 244
  • [42] Points of control in inflammation
    Nathan, C
    [J]. NATURE, 2002, 420 (6917) : 846 - 852
  • [43] Progressive periodontal disease and risk of very preterm delivery
    Offenbacher, S
    Boggess, KA
    Murtha, AP
    Jared, HL
    Lieff, S
    McKaig, RG
    Mauriello, SM
    Moss, KL
    Beck, JD
    [J]. OBSTETRICS AND GYNECOLOGY, 2006, 107 (01) : 29 - 36
  • [44] Offenbacher S, 1993, Adv Dent Res, V7, P175
  • [45] MODULATION OF HOST PGE2 SECRETION AS A DETERMINANT OF PERIODONTAL-DISEASE EXPRESSION
    OFFENBACHER, S
    HEASMAN, PA
    COLLINS, JG
    [J]. JOURNAL OF PERIODONTOLOGY, 1993, 64 (05) : 432 - 444
  • [46] Offenbacher S, 1996, Ann Periodontol, V1, P821, DOI 10.1902/annals.1996.1.1.821
  • [47] THE USE OF CREVICULAR FLUID PROSTAGLANDIN-E2 LEVELS AS A PREDICTOR OF PERIODONTAL ATTACHMENT LOSS
    OFFENBACHER, S
    ODLE, BM
    VANDYKE, TE
    [J]. JOURNAL OF PERIODONTAL RESEARCH, 1986, 21 (02) : 101 - 112
  • [48] Park Yong-Koo, 1995, Journal of Korean Medical Science, V10, P263
  • [49] Lipoxin A4 analogues inhibit leukocyte recruitment to Porphyromonas gingivalis:: A role for cyclooxygenase-2 and lipoxins in periodontal disease
    Pouliot, M
    Clish, CB
    Petasis, NA
    Van Dyke, TE
    Serhan, CN
    [J]. BIOCHEMISTRY, 2000, 39 (16) : 4761 - 4768
  • [50] Ridker PM, 1998, CIRCULATION, V97, P425