The role of Lipoxin A4 in endometrial biology and endometriosis

被引:35
作者
Canny, G. O. [1 ]
Lessey, B. A. [2 ]
机构
[1] Geneva Fdn Med Educ & Res, Versoix, Switzerland
[2] Univ S Carolina, Sch Med Greenville, Greenville, SC USA
基金
瑞士国家科学基金会;
关键词
ESTROGEN-RECEPTOR-ALPHA; PROLIFERATOR-ACTIVATED RECEPTOR; ARYL-HYDROCARBON RECEPTOR; MESSENGER-RNA EXPRESSION; NECROSIS-FACTOR-ALPHA; PROGESTERONE-RECEPTORS; GENE-EXPRESSION; IMMUNOHISTOCHEMICAL ANALYSIS; UTERINE RECEPTIVITY; PROSTAGLANDIN E-2;
D O I
10.1038/mi.2013.9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lipoxin A(4) ( LXA(4)), an endogenous anti-inflammatory and immunomodulatory mediator studied in many disease states, is recently appreciated as a potentially significant player in the endometrium. This eicosanoid, synthesized from arachidonic acid via the action of lipoxygenase enzymes, is likely regulated in endometrial tissue during the menstrual cycle. Recent studies revealed that LXA(4) acts as an estrogen receptor agonist in endometrial epithelial cells, antagonizing some estrogen-mediated activities in a manner similar to the weak estrogen estriol, with which it shares structural similarity. LXA(4) may also be an anti-inflammatory molecule in the endometrium, though its precise function in various physiological and pathological scenarios remains to be determined. The expression patterns for LXA(4) and its receptor in the female reproductive tract suggest a role in pregnancy. The present review provides an oversight of its known and putative roles in the context of immuno-endocrine crosstalk. Endometriosis, a common inflammatory condition and a major cause of infertility and pain, is currently treated by surgery or anti-hormone therapies that are contraceptive and associated with undesirable side effects. LXA(4) may represent a potential therapeutic and further research to elucidate its function in endometrial tissue and the peritoneal cavity will undoubtedly provide valuable insights.
引用
收藏
页码:439 / 450
页数:12
相关论文
共 202 条
[161]   Resolving inflammation: dual anti-inflammatory and pro-resolution lipid mediators [J].
Serhan, Charles N. ;
Chiang, Nan ;
Van Dyke, Thomas E. .
NATURE REVIEWS IMMUNOLOGY, 2008, 8 (05) :349-361
[162]   Resolution phase of inflammation: Novel endogenous anti-inflammatory and proresolving lipid mediators and pathways [J].
Serhan, Charles N. .
ANNUAL REVIEW OF IMMUNOLOGY, 2007, 25 :101-137
[163]   Controlling the Resolution of Acute Inflammation: A New Genus of Dual Anti-Inflammatory and Proresolving Mediators [J].
Serhan, Charles N. .
JOURNAL OF PERIODONTOLOGY, 2008, 79 (08) :1520-1526
[164]   Resolution of inflammation: The beginning programs the end [J].
Serhan, CN ;
Savill, J .
NATURE IMMUNOLOGY, 2005, 6 (12) :1191-1197
[165]   Macrophages, Meta-Inflammation, and Immuno-Metabolism [J].
Shapiro, Haim ;
Lutaty, Aviv ;
Ariel, Amiram .
THESCIENTIFICWORLDJOURNAL, 2011, 11 :2509-2529
[166]   Macrophage plasticity and polarization: in vivo veritas [J].
Sica, Antonio ;
Mantovani, Alberto .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (03) :787-795
[167]   Hormonal regulation and localization of estrogen, progestin and androgen receptors in the endometrium of nonhuman primates: effects of progesterone receptor antagonists [J].
Slayden, OD ;
Brenner, RM .
ARCHIVES OF HISTOLOGY AND CYTOLOGY, 2004, 67 (05) :393-409
[168]  
Smith KA, 2012, COMPARATIVE MED, V62, P303
[169]   Lipoxin A4 inhibits IL-1β-induced IL-6, IL-8, and matrix metalloproteinase-3 production in human synovial fibroblasts and enhances synthesis of tissue inhibitors of metalloproteinases [J].
Sodin-Semrl, S ;
Taddeo, B ;
Tseng, D ;
Varga, J ;
Fiore, S .
JOURNAL OF IMMUNOLOGY, 2000, 164 (05) :2660-2666
[170]   Adhesion Prevention in Endometriosis: A Neglected Critical Challenge [J].
Somigliana, Edgardo ;
Vigano, Paola ;
Benaglia, Laura ;
Busnelli, Andrea ;
Vercellini, Paolo ;
Fedele, Luigi .
JOURNAL OF MINIMALLY INVASIVE GYNECOLOGY, 2012, 19 (04) :415-421