Back to Search
Start Over
Estradiol promotes M1-like macrophage activation through cadherin-11 to aggravate temporomandibular joint inflammation in rats.
- Source :
-
Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2015 Mar 15; Vol. 194 (6), pp. 2810-8. Date of Electronic Publication: 2015 Feb 13. - Publication Year :
- 2015
-
Abstract
- Macrophages play a major role in joint inflammation. Estrogen is involved in rheumatoid arthritis and temporomandibular disorders. However, the underlying mechanism is still unclear. This study was done to verify and test how estrogen affects M1/M2-like macrophage polarization and then contributes to joint inflammation. Female rats were ovariectomized and treated with increasing doses of 17β-estradiol for 10 d and then intra-articularly injected with CFA to induce temporomandibular joint (TMJ) inflammation. The polarization of macrophages and expression of cadherin-11 was evaluated at 24 h after the induction of TMJ inflammation and after blocking cadherin-11 or estrogen receptors. NR8383 macrophages were treated with estradiol and TNF-α, with or without blocking cadherin-11 or estrogen receptors, to evaluate the expression of the M1/M2-like macrophage-associated genes. We found that estradiol increased the infiltration of macrophages with a proinflammatory M1-like predominant profile in the synovium of inflamed TMJ. In addition, estradiol dose-dependently upregulated the expressions of the M1-associated proinflammatory factor inducible NO synthase (iNOS) but repressed the expressions of the M2-associated genes IL-10 and arginase in NR8383 macrophages. Furthermore, estradiol mainly promoted cadherin-11 expression in M1-like macrophages of inflamed TMJ. By contrast, blockage of cadherin-11 concurrently reversed estradiol-potentiated M1-like macrophage activation and TMJ inflammation, as well as reversed TNF-α-induced induction of inducible NO synthase and NO in NR8383 macrophages. The blocking of estrogen receptors reversed estradiol-potentiated M1-like macrophage activation and cadherin-11 expression. These results suggested that estradiol could promote M1-like macrophage activation through cadherin-11 to aggravate the acute inflammation of TMJs.<br /> (Copyright © 2015 by The American Association of Immunologists, Inc.)
- Subjects :
- Animals
Arginase genetics
Arginase immunology
Arginase metabolism
Arthritis genetics
Arthritis immunology
Arthritis metabolism
Blotting, Western
Cadherins genetics
Cadherins metabolism
Estradiol analogs & derivatives
Estradiol pharmacology
Estrogen Receptor Antagonists pharmacology
Estrogens immunology
Estrogens pharmacology
Female
Fulvestrant
Gene Expression drug effects
Gene Expression immunology
Inflammation genetics
Inflammation metabolism
Interleukin-10 genetics
Interleukin-10 immunology
Interleukin-10 metabolism
Macrophage Activation drug effects
Macrophages drug effects
Macrophages metabolism
Microscopy, Confocal
Nitric Oxide immunology
Nitric Oxide metabolism
Nitric Oxide Synthase Type II genetics
Nitric Oxide Synthase Type II immunology
Nitric Oxide Synthase Type II metabolism
Ovariectomy
Rats, Sprague-Dawley
Receptors, Estrogen antagonists & inhibitors
Receptors, Estrogen immunology
Receptors, Estrogen metabolism
Reverse Transcriptase Polymerase Chain Reaction
Temporomandibular Joint drug effects
Temporomandibular Joint pathology
Tumor Necrosis Factor-alpha immunology
Tumor Necrosis Factor-alpha pharmacology
Cadherins immunology
Estradiol immunology
Inflammation immunology
Macrophage Activation immunology
Macrophages immunology
Temporomandibular Joint immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1550-6606
- Volume :
- 194
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Journal of immunology (Baltimore, Md. : 1950)
- Publication Type :
- Academic Journal
- Accession number :
- 25681337
- Full Text :
- https://doi.org/10.4049/jimmunol.1303188