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 inOral diseases Vol. 24; no. 8; pp. 1503 - 1513
Main Authors Xue, Xin‐Tong, Zhang, Ting, Cui, Sheng‐Jie, He, Dan‐Qing, Wang, Xue‐Dong, Yang, Rui‐Li, Liu, Da‐Wei, Liu, Yan, Gan, Ye‐Hua, Kou, Xiao‐Xing, Zhou, Yan‐Heng
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Published Denmark Wiley Subscription Services, Inc 01.11.2018
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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.
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
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Keywords estrogen
Temporomandibular joint osteoarthritis
sexual dimorphism
synovitis
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Snippet Objectives 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
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fodi.12905
https://www.ncbi.nlm.nih.gov/pubmed/29806726
https://www.proquest.com/docview/2121371362
https://www.proquest.com/docview/2046014100
Volume 24
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