Sexual dimorphism of estrogen‐sensitized synoviocytes contributes to gender difference in temporomandibular joint osteoarthritis
Objectives Temporomandibular joint osteoarthritis (TMJOA) is approximately twice as prevalent in women than in men. Synoviocytes are believed to play a critical role in joint inflammation. However, it is unknown whether synoviocytes from different genders possess sexual dimorphisms that contribute t...
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Published in | Oral diseases Vol. 24; no. 8; pp. 1503 - 1513 |
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Main Authors | , , , , , , , , , , |
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Abstract | Objectives
Temporomandibular joint osteoarthritis (TMJOA) is approximately twice as prevalent in women than in men. Synoviocytes are believed to play a critical role in joint inflammation. However, it is unknown whether synoviocytes from different genders possess sexual dimorphisms that contribute to female‐predominant TMJOA.
Materials and Methods
Freund's complete adjuvant combined with monosodium iodoacetate was used to induce TMJOA in female and male rats. Histologic and radiographic features were used to evaluate TMJOA. The expression of CD68, MCP‐1, iNOS, and IL‐1β was detected by immunohistochemistry and real‐time PCR. Primary fibroblast‐like synoviocytes (FLSs) isolated from the synovial membrane of female and male rats were used for in vitro experiments.
Results
Female rats showed aggravated TMJOA features as compared to male rats. Increased expression of iNOS and IL‐1β was detected in synovial membrane from female TMJOA rats as compared to male rats. Furthermore, greater amounts of CD68‐positive macrophage infiltration and increased MCP‐1 expression around the synovial membrane were detected in female TMJOA rats compared to males. Primary cultured FLSs from female rats showed higher sensitivity to TNF‐α treatment and recruited increased macrophage migration than male FLSs. More important, ovariectomy (OVX) by ablation in female rats repressed the sensitivity of female FLSs to TNF‐α treatment due to the loss of estrogen production. Blockage of the estrogen receptor repressed estrogen‐potentiated TNF‐α‐induced pro‐inflammatory cytokine expression in OVX‐FLSs. Moreover, the injection of estrogen receptor antagonists relieved the cartilage destruction and bone deterioration of TMJOA in female rats.
Conclusion
Estrogen‐sensitized synoviocytes in female rats may contribute to gender differences in the incidence and progression of TMJOA. |
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AbstractList | Temporomandibular joint osteoarthritis (TMJOA) is approximately twice as prevalent in women than in men. Synoviocytes are believed to play a critical role in joint inflammation. However, it is unknown whether synoviocytes from different genders possess sexual dimorphisms that contribute to female-predominant TMJOA.OBJECTIVESTemporomandibular joint osteoarthritis (TMJOA) is approximately twice as prevalent in women than in men. Synoviocytes are believed to play a critical role in joint inflammation. However, it is unknown whether synoviocytes from different genders possess sexual dimorphisms that contribute to female-predominant TMJOA.Freund's complete adjuvant combined with monosodium iodoacetate was used to induce TMJOA in female and male rats. Histologic and radiographic features were used to evaluate TMJOA. The expression of CD68, MCP-1, iNOS, and IL-1β was detected by immunohistochemistry and real-time PCR. Primary fibroblast-like synoviocytes (FLSs) isolated from the synovial membrane of female and male rats were used for in vitro experiments.MATERIALS AND METHODSFreund's complete adjuvant combined with monosodium iodoacetate was used to induce TMJOA in female and male rats. Histologic and radiographic features were used to evaluate TMJOA. The expression of CD68, MCP-1, iNOS, and IL-1β was detected by immunohistochemistry and real-time PCR. Primary fibroblast-like synoviocytes (FLSs) isolated from the synovial membrane of female and male rats were used for in vitro experiments.Female rats showed aggravated TMJOA features as compared to male rats. Increased expression of iNOS and IL-1β was detected in synovial membrane from female TMJOA rats as compared to male rats. Furthermore, greater amounts of CD68-positive macrophage infiltration and increased MCP-1 expression around the synovial membrane were detected in female TMJOA rats compared to males. Primary cultured FLSs from female rats showed higher sensitivity to TNF-α treatment and recruited increased macrophage migration than male FLSs. More important, ovariectomy (OVX) by ablation in female rats repressed the sensitivity of female FLSs to TNF-α treatment due to the loss of estrogen production. Blockage of the estrogen receptor repressed estrogen-potentiated TNF-α-induced pro-inflammatory cytokine expression in OVX-FLSs. Moreover, the injection of estrogen receptor antagonists relieved the cartilage destruction and bone deterioration of TMJOA in female rats.RESULTSFemale rats showed aggravated TMJOA features as compared to male rats. Increased expression of iNOS and IL-1β was detected in synovial membrane from female TMJOA rats as compared to male rats. Furthermore, greater amounts of CD68-positive macrophage infiltration and increased MCP-1 expression around the synovial membrane were detected in female TMJOA rats compared to males. Primary cultured FLSs from female rats showed higher sensitivity to TNF-α treatment and recruited increased macrophage migration than male FLSs. More important, ovariectomy (OVX) by ablation in female rats repressed the sensitivity of female FLSs to TNF-α treatment due to the loss of estrogen production. Blockage of the estrogen receptor repressed estrogen-potentiated TNF-α-induced pro-inflammatory cytokine expression in OVX-FLSs. Moreover, the injection of estrogen receptor antagonists relieved the cartilage destruction and bone deterioration of TMJOA in female rats.Estrogen-sensitized synoviocytes in female rats may contribute to gender differences in the incidence and progression of TMJOA.CONCLUSIONEstrogen-sensitized synoviocytes in female rats may contribute to gender differences in the incidence and progression of TMJOA. ObjectivesTemporomandibular joint osteoarthritis (TMJOA) is approximately twice as prevalent in women than in men. Synoviocytes are believed to play a critical role in joint inflammation. However, it is unknown whether synoviocytes from different genders possess sexual dimorphisms that contribute to female‐predominant TMJOA.Materials and MethodsFreund's complete adjuvant combined with monosodium iodoacetate was used to induce TMJOA in female and male rats. Histologic and radiographic features were used to evaluate TMJOA. The expression of CD68, MCP‐1, iNOS, and IL‐1β was detected by immunohistochemistry and real‐time PCR. Primary fibroblast‐like synoviocytes (FLSs) isolated from the synovial membrane of female and male rats were used for in vitro experiments.ResultsFemale rats showed aggravated TMJOA features as compared to male rats. Increased expression of iNOS and IL‐1β was detected in synovial membrane from female TMJOA rats as compared to male rats. Furthermore, greater amounts of CD68‐positive macrophage infiltration and increased MCP‐1 expression around the synovial membrane were detected in female TMJOA rats compared to males. Primary cultured FLSs from female rats showed higher sensitivity to TNF‐α treatment and recruited increased macrophage migration than male FLSs. More important, ovariectomy (OVX) by ablation in female rats repressed the sensitivity of female FLSs to TNF‐α treatment due to the loss of estrogen production. Blockage of the estrogen receptor repressed estrogen‐potentiated TNF‐α‐induced pro‐inflammatory cytokine expression in OVX‐FLSs. Moreover, the injection of estrogen receptor antagonists relieved the cartilage destruction and bone deterioration of TMJOA in female rats.ConclusionEstrogen‐sensitized synoviocytes in female rats may contribute to gender differences in the incidence and progression of TMJOA. Objectives Temporomandibular joint osteoarthritis (TMJOA) is approximately twice as prevalent in women than in men. Synoviocytes are believed to play a critical role in joint inflammation. However, it is unknown whether synoviocytes from different genders possess sexual dimorphisms that contribute to female‐predominant TMJOA. Materials and Methods Freund's complete adjuvant combined with monosodium iodoacetate was used to induce TMJOA in female and male rats. Histologic and radiographic features were used to evaluate TMJOA. The expression of CD68, MCP‐1, iNOS, and IL‐1β was detected by immunohistochemistry and real‐time PCR. Primary fibroblast‐like synoviocytes (FLSs) isolated from the synovial membrane of female and male rats were used for in vitro experiments. Results Female rats showed aggravated TMJOA features as compared to male rats. Increased expression of iNOS and IL‐1β was detected in synovial membrane from female TMJOA rats as compared to male rats. Furthermore, greater amounts of CD68‐positive macrophage infiltration and increased MCP‐1 expression around the synovial membrane were detected in female TMJOA rats compared to males. Primary cultured FLSs from female rats showed higher sensitivity to TNF‐α treatment and recruited increased macrophage migration than male FLSs. More important, ovariectomy (OVX) by ablation in female rats repressed the sensitivity of female FLSs to TNF‐α treatment due to the loss of estrogen production. Blockage of the estrogen receptor repressed estrogen‐potentiated TNF‐α‐induced pro‐inflammatory cytokine expression in OVX‐FLSs. Moreover, the injection of estrogen receptor antagonists relieved the cartilage destruction and bone deterioration of TMJOA in female rats. Conclusion Estrogen‐sensitized synoviocytes in female rats may contribute to gender differences in the incidence and progression of TMJOA. Temporomandibular joint osteoarthritis (TMJOA) is approximately twice as prevalent in women than in men. Synoviocytes are believed to play a critical role in joint inflammation. However, it is unknown whether synoviocytes from different genders possess sexual dimorphisms that contribute to female-predominant TMJOA. Freund's complete adjuvant combined with monosodium iodoacetate was used to induce TMJOA in female and male rats. Histologic and radiographic features were used to evaluate TMJOA. The expression of CD68, MCP-1, iNOS, and IL-1β was detected by immunohistochemistry and real-time PCR. Primary fibroblast-like synoviocytes (FLSs) isolated from the synovial membrane of female and male rats were used for in vitro experiments. Female rats showed aggravated TMJOA features as compared to male rats. Increased expression of iNOS and IL-1β was detected in synovial membrane from female TMJOA rats as compared to male rats. Furthermore, greater amounts of CD68-positive macrophage infiltration and increased MCP-1 expression around the synovial membrane were detected in female TMJOA rats compared to males. Primary cultured FLSs from female rats showed higher sensitivity to TNF-α treatment and recruited increased macrophage migration than male FLSs. More important, ovariectomy (OVX) by ablation in female rats repressed the sensitivity of female FLSs to TNF-α treatment due to the loss of estrogen production. Blockage of the estrogen receptor repressed estrogen-potentiated TNF-α-induced pro-inflammatory cytokine expression in OVX-FLSs. Moreover, the injection of estrogen receptor antagonists relieved the cartilage destruction and bone deterioration of TMJOA in female rats. Estrogen-sensitized synoviocytes in female rats may contribute to gender differences in the incidence and progression of TMJOA. |
Author | Liu, Yan Zhang, Ting Zhou, Yan‐Heng Wang, Xue‐Dong Xue, Xin‐Tong He, Dan‐Qing Kou, Xiao‐Xing Yang, Rui‐Li Cui, Sheng‐Jie Liu, Da‐Wei Gan, Ye‐Hua |
Author_xml | – sequence: 1 givenname: Xin‐Tong orcidid: 0000-0001-5723-3030 surname: Xue fullname: Xue, Xin‐Tong organization: Peking University School and Hospital of Stomatology – sequence: 2 givenname: Ting surname: Zhang fullname: Zhang, Ting organization: Peking University School and Hospital of Stomatology – sequence: 3 givenname: Sheng‐Jie surname: Cui fullname: Cui, Sheng‐Jie organization: Peking University School and Hospital of Stomatology – sequence: 4 givenname: Dan‐Qing surname: He fullname: He, Dan‐Qing organization: Peking University School and Hospital of Stomatology – sequence: 5 givenname: Xue‐Dong surname: Wang fullname: Wang, Xue‐Dong organization: Peking University School and Hospital of Stomatology – sequence: 6 givenname: Rui‐Li surname: Yang fullname: Yang, Rui‐Li organization: Peking University School and Hospital of Stomatology – sequence: 7 givenname: Da‐Wei surname: Liu fullname: Liu, Da‐Wei organization: Peking University School and Hospital of Stomatology – sequence: 8 givenname: Yan surname: Liu fullname: Liu, Yan organization: Peking University School and Hospital of Stomatology – sequence: 9 givenname: Ye‐Hua surname: Gan fullname: Gan, Ye‐Hua organization: Peking University School and Hospital of Stomatology – sequence: 10 givenname: Xiao‐Xing surname: Kou fullname: Kou, Xiao‐Xing email: kouxiaoxing@gmail.com organization: Peking University School and Hospital of Stomatology – sequence: 11 givenname: Yan‐Heng surname: Zhou fullname: Zhou, Yan‐Heng email: yanhengzhou@vip.163.com organization: Peking University School and Hospital of Stomatology |
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Cites_doi | 10.1152/ajpregu.00835.2005 10.1177/0022034512441946 10.1679/aohc.66.289 10.1097/00002508-200103000-00004 10.1371/journal.pone.0045036 10.1056/NEJMra052723 10.1016/S0278-2391(98)90246-4 10.1016/j.joca.2008.09.015 10.1002/path.1758 10.3132/pcrj.2007.00006 10.1155/2015/630265 10.1111/j.1600-0714.2006.00369.x 10.1016/0278-2391(89)90227-9 10.1182/blood-2007-12-077917 10.1038/ni1001-907 10.1007/s11897-012-0107-7 10.1016/j.jsbmb.2005.05.013 10.1016/j.jsbmb.2014.07.002 10.1016/j.atherosclerosis.2015.02.018 10.4161/epi.6.6.16177 10.1038/nri2448 10.1186/s13293-016-0113-7 10.1177/0022034510376041 10.1523/JNEUROSCI.6323-09.2010 10.1002/art.30334 10.1002/jbmr.37 10.1186/1477-7827-7-155 10.1002/1529-0131(200012)43:12<2619::AID-ANR1>3.0.CO;2-V 10.4049/jimmunol.1303188 10.1016/j.jpain.2012.09.009 10.1177/0022034513501323 |
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Keywords | estrogen Temporomandibular joint osteoarthritis sexual dimorphism synovitis |
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References | 2015; 240 2006; 35 2000; 43 2008; 8 2013; 92 2006; 291 2012; 13 2011; 6 1989; 47 2006; 354 2007; 16 1992; 6 2010; 89 2015; 194 2016; 7 2012; 91 2006; 41 2010; 25 1999; 13 2005; 206 2015; 2015 2011; 63 2005; 97 2009; 7 2001; 2 2001; 17 2008; 112 2014; 143 2012; 7 1998; 56 2010; 30 2003; 66 2012; 9 2009; 17 e_1_2_8_28_1 e_1_2_8_29_1 e_1_2_8_24_1 e_1_2_8_25_1 e_1_2_8_26_1 e_1_2_8_27_1 Dworkin S. F. (e_1_2_8_8_1) 1992; 6 e_1_2_8_2_1 e_1_2_8_5_1 e_1_2_8_4_1 e_1_2_8_7_1 e_1_2_8_6_1 e_1_2_8_9_1 Zhao Y. P. (e_1_2_8_36_1) 2006; 41 e_1_2_8_20_1 e_1_2_8_21_1 e_1_2_8_22_1 e_1_2_8_23_1 e_1_2_8_17_1 e_1_2_8_18_1 e_1_2_8_19_1 e_1_2_8_13_1 e_1_2_8_14_1 e_1_2_8_15_1 e_1_2_8_16_1 Zarb G. A. (e_1_2_8_35_1) 1999; 13 Carlsson G. E. (e_1_2_8_3_1) 1999; 13 e_1_2_8_32_1 e_1_2_8_10_1 e_1_2_8_31_1 e_1_2_8_11_1 e_1_2_8_34_1 e_1_2_8_12_1 e_1_2_8_33_1 e_1_2_8_30_1 |
References_xml | – volume: 291 start-page: R343 year: 2006 end-page: R348 article-title: Testosterone and estrogen have opposing actions on inflammation‐induced plasma extravasation in the rat temporomandibular joint publication-title: American Journal of Physiology: Regulatory, Integrative and Comparative Physiology – volume: 112 start-page: 935 year: 2008 end-page: 945 article-title: The phagocytes: Neutrophils and monocytes publication-title: Blood – volume: 7 start-page: 60 year: 2016 article-title: Sexual dimorphism in the mast cell transcriptome and the pathophysiological responses to immunological and psychological stress publication-title: Biology of Sex Differences – volume: 6 start-page: 675 year: 2011 end-page: 680 article-title: The epigenetics of estrogen: Epigenetic regulation of hormone‐induced memory enhancement publication-title: Epigenetics – volume: 47 start-page: 249 year: 1989 end-page: 256 article-title: Osteoarthrosis as the cause of craniomandibular pain and dysfunction: A unifying concept publication-title: Journal of Oral and Maxillofacial Surgery – volume: 9 start-page: 267 year: 2012 end-page: 276 article-title: Gender differences in the pathophysiology, clinical presentation, and outcomes of ischemic heart failure publication-title: Current Heart Failure Reports – volume: 13 start-page: 1224 year: 2012 end-page: 1231 article-title: In vivo and in vitro comparison of female and male nociceptors publication-title: The Journal of Pain: Official Journal of The American Pain Society – volume: 56 start-page: 1023 year: 1998 end-page: 1027 article-title: Osteoarthritis and synovitis as major pathoses of the temporomandibular joint: Comparison of clinical diagnosis with arthroscopic morphology publication-title: Journal of Oral and Maxillofacial Surgery – volume: 143 start-page: 444 year: 2014 end-page: 450 article-title: Estradiol‐potentiated cadherin‐11 in synovial membrane involves in temporomandibular joint inflammation in rats publication-title: Journal of Steroid Biochemistry and Molecular Biology – volume: 43 start-page: 2619 year: 2000 end-page: 2633 article-title: The pathogenesis and prevention of joint damage in rheumatoid arthritis: Advances from synovial biopsy and tissue analysis publication-title: Arthritis and Rheumatism – volume: 63 start-page: 1888 year: 2011 end-page: 1897 article-title: 17beta‐estradiol aggravates temporomandibular joint inflammation through the NF‐kappaB pathway in ovariectomized rats publication-title: Arthritis and Rheumatism – volume: 7 start-page: 155 year: 2009 article-title: Estrogen and inflammation modulate estrogen receptor alpha expression in specific tissues of the temporomandibular joint publication-title: Reproductive Biology and Endocrinology – volume: 354 start-page: 610 year: 2006 end-page: 621 article-title: The many roles of chemokines and chemokine receptors in inflammation publication-title: New England Journal of Medicine – volume: 17 start-page: 646 year: 2009 end-page: 654 article-title: Female hormone receptors are differentially expressed in mouse fibrocartilages publication-title: Osteoarthritis Cartilage – volume: 89 start-page: 1117 year: 2010 end-page: 1122 article-title: MCP‐1 production in temporomandibular joint inflammation publication-title: Journal of Dental Research – volume: 8 start-page: 958 year: 2008 end-page: 969 article-title: Exploring the full spectrum of macrophage activation publication-title: Nature Reviews Immunology – volume: 25 start-page: 1668 year: 2010 end-page: 1679 article-title: Cell‐based immunotherapy with mesenchymal stem cells cures bisphosphonate‐related osteonecrosis of the jaw‐like disease in mice publication-title: Journal of Bone and Mineral Research – volume: 194 start-page: 2810 year: 2015 end-page: 2818 article-title: Estradiol promotes M1‐like macrophage activation through cadherin‐11 to aggravate temporomandibular joint inflammation in rats publication-title: The Journal of Immunology – volume: 16 start-page: 28 year: 2007 end-page: 35 article-title: Gender‐specific presentations for asthma, allergic rhinitis and eczema in primary care publication-title: Primary Care Respiratory Journal – volume: 2 start-page: 907 year: 2001 end-page: 916 article-title: Nitric oxide and the immune response publication-title: Nature Immunology – volume: 13 start-page: 295 year: 1999 end-page: 306 article-title: Temporomandibular disorders: Osteoarthritis publication-title: Journal of Orofacial Pain – volume: 92 start-page: 918 year: 2013 end-page: 924 article-title: Estrogen aggravates iodoacetate‐induced temporomandibular joint osteoarthritis publication-title: Journal of Dental Research – volume: 2015 start-page: 630265 year: 2015 article-title: Interleukin‐1 family cytokines in liver diseases publication-title: Mediators of Inflammation – volume: 30 start-page: 8710 year: 2010 end-page: 8719 article-title: 17‐Beta‐estradiol enhanced allodynia of inflammatory temporomandibular joint through upregulation of hippocampal TRPV1 in ovariectomized rats publication-title: Journal of Neuroscience – volume: 17 start-page: 20 year: 2001 end-page: 24 article-title: Sex differences in musculoskeletal pain publication-title: Clinical Journal of Pain – volume: 41 start-page: 757 year: 2006 end-page: 758 article-title: Temporomandibular disorders related pain interaction with age, sex and imaging changes of osteoarthrosis publication-title: Zhonghua Kou Qiang Yi Xue Za Zhi – volume: 35 start-page: 104 year: 2006 end-page: 110 article-title: Isolation and characterization of synovial cells from the human temporomandibular joint publication-title: Journal of Oral Pathology and Medicine – volume: 206 start-page: 17 year: 2005 end-page: 27 article-title: Differential expression and response to anti‐TNFalpha treatment of infiltrating versus resident tissue macrophage subsets in autoimmune arthritis publication-title: The Journal of Pathology – volume: 6 start-page: 301 year: 1992 end-page: 355 article-title: Research diagnostic criteria for temporomandibular disorders: Review, criteria, examinations and specifications, critique publication-title: Journal of Craniomandibular Disorders : Facial & Oral Pain – volume: 7 start-page: e45036 year: 2012 article-title: Progression of cartilage degradation, bone resorption and pain in rat temporomandibular joint osteoarthritis induced by injection of iodoacetate publication-title: PLoS One – volume: 91 start-page: 499 year: 2012 end-page: 505 article-title: Sustained inflammation induces degeneration of the temporomandibular joint publication-title: Journal of Dental Research – volume: 97 start-page: 241 year: 2005 end-page: 250 article-title: Estrogenic effect on swelling and monocytic receptor expression in an arthritic temporomandibular joint model publication-title: Journal of Steroid Biochemistry and Molecular Biology – volume: 66 start-page: 289 year: 2003 end-page: 306 article-title: Synovial membrane in the temporomandibular joint–its morphology, function and development publication-title: Archives of Histology and Cytology – volume: 240 start-page: 61 year: 2015 end-page: 72 article-title: Does cellular sex matter? Dimorphic transcriptional differences between female and male endothelial cells publication-title: Atherosclerosis – volume: 13 start-page: 232 year: 1999 end-page: 237 article-title: Epidemiology and treatment need for temporomandibular disorders publication-title: Journal of Orofacial Pain – ident: e_1_2_8_9_1 doi: 10.1152/ajpregu.00835.2005 – ident: e_1_2_8_32_1 doi: 10.1177/0022034512441946 – ident: e_1_2_8_22_1 doi: 10.1679/aohc.66.289 – ident: e_1_2_8_26_1 doi: 10.1097/00002508-200103000-00004 – ident: e_1_2_8_31_1 doi: 10.1371/journal.pone.0045036 – ident: e_1_2_8_4_1 doi: 10.1056/NEJMra052723 – ident: e_1_2_8_13_1 doi: 10.1016/S0278-2391(98)90246-4 – ident: e_1_2_8_30_1 doi: 10.1016/j.joca.2008.09.015 – ident: e_1_2_8_6_1 doi: 10.1002/path.1758 – volume: 6 start-page: 301 year: 1992 ident: e_1_2_8_8_1 article-title: Research diagnostic criteria for temporomandibular disorders: Review, criteria, examinations and specifications, critique publication-title: Journal of Craniomandibular Disorders : Facial & Oral Pain – ident: e_1_2_8_24_1 doi: 10.3132/pcrj.2007.00006 – ident: e_1_2_8_29_1 doi: 10.1155/2015/630265 – ident: e_1_2_8_21_1 doi: 10.1111/j.1600-0714.2006.00369.x – ident: e_1_2_8_27_1 doi: 10.1016/0278-2391(89)90227-9 – ident: e_1_2_8_5_1 doi: 10.1182/blood-2007-12-077917 – volume: 41 start-page: 757 year: 2006 ident: e_1_2_8_36_1 article-title: Temporomandibular disorders related pain interaction with age, sex and imaging changes of osteoarthrosis publication-title: Zhonghua Kou Qiang Yi Xue Za Zhi – ident: e_1_2_8_2_1 doi: 10.1038/ni1001-907 – ident: e_1_2_8_7_1 doi: 10.1007/s11897-012-0107-7 – ident: e_1_2_8_11_1 doi: 10.1016/j.jsbmb.2005.05.013 – volume: 13 start-page: 295 year: 1999 ident: e_1_2_8_35_1 article-title: Temporomandibular disorders: Osteoarthritis publication-title: Journal of Orofacial Pain – ident: e_1_2_8_16_1 doi: 10.1016/j.jsbmb.2014.07.002 – ident: e_1_2_8_18_1 doi: 10.1016/j.atherosclerosis.2015.02.018 – ident: e_1_2_8_10_1 doi: 10.4161/epi.6.6.16177 – ident: e_1_2_8_20_1 doi: 10.1038/nri2448 – ident: e_1_2_8_19_1 doi: 10.1186/s13293-016-0113-7 – ident: e_1_2_8_23_1 doi: 10.1177/0022034510376041 – ident: e_1_2_8_34_1 doi: 10.1523/JNEUROSCI.6323-09.2010 – ident: e_1_2_8_17_1 doi: 10.1002/art.30334 – ident: e_1_2_8_14_1 doi: 10.1002/jbmr.37 – ident: e_1_2_8_25_1 doi: 10.1186/1477-7827-7-155 – volume: 13 start-page: 232 year: 1999 ident: e_1_2_8_3_1 article-title: Epidemiology and treatment need for temporomandibular disorders publication-title: Journal of Orofacial Pain – ident: e_1_2_8_28_1 doi: 10.1002/1529-0131(200012)43:12<2619::AID-ANR1>3.0.CO;2-V – ident: e_1_2_8_15_1 doi: 10.4049/jimmunol.1303188 – ident: e_1_2_8_12_1 doi: 10.1016/j.jpain.2012.09.009 – ident: e_1_2_8_33_1 doi: 10.1177/0022034513501323 |
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Temporomandibular joint osteoarthritis (TMJOA) is approximately twice as prevalent in women than in men. Synoviocytes are believed to play a... Temporomandibular joint osteoarthritis (TMJOA) is approximately twice as prevalent in women than in men. Synoviocytes are believed to play a critical role in... ObjectivesTemporomandibular joint osteoarthritis (TMJOA) is approximately twice as prevalent in women than in men. Synoviocytes are believed to play a critical... |
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SubjectTerms | Animals Antigens, CD - metabolism Antigens, Differentiation, Myelomonocytic - metabolism Arthritis Cartilage diseases Cell Movement - drug effects Cells, Cultured Chemokine CCL2 - metabolism estrogen Estrogen Receptor Antagonists - pharmacology Estrogens - metabolism Estrogens - pharmacology Female Immunohistochemistry Inflammation Interleukin-1beta - metabolism Leukocyte migration Macrophages Macrophages - metabolism Macrophages - physiology Male Nitric Oxide Synthase Type II - metabolism Nitric-oxide synthase Osteoarthritis Osteoarthritis - metabolism Osteoarthritis - pathology Ovariectomy Rats Rats, Sprague-Dawley Receptors, Estrogen - antagonists & inhibitors Rodents Sex differences Sex Factors Sexual dimorphism Synovial membrane Synovial Membrane - metabolism Synoviocytes Synoviocytes - drug effects Synoviocytes - metabolism synovitis Temporomandibular joint Temporomandibular Joint Disorders - metabolism Temporomandibular joint osteoarthritis Tumor necrosis factor Tumor Necrosis Factor-alpha - pharmacology |
Title | Sexual dimorphism of estrogen‐sensitized synoviocytes contributes to gender difference in temporomandibular joint osteoarthritis |
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