Effects of estradiol on proliferation and metabolism of rabbit mandibular condylar cartilage cells in vitro
Objective To investigate the effects in vitro of 17β-estradiol ( E2 ) on the proliferation and metabolism of rabbit mandibular condylar cartilage cells.Methods Chondrocytes were derived from neonatal rabbit mandibular condylar cartilage using a modified enzyme method. 17β-estradiol was added to the...
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Published in | Chinese medical journal Vol. 116; no. 9; pp. 1413 - 1417 |
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Format | Journal Article |
Language | English |
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China
Center for Temporomandibular Disorders, Peking University School of Stomatology, Beijing 100081, China%Laboratory of Molecular Biology, Beijing Jishuitan Hospital, Beijing 100083, China%Laboratory of Oral and Maxillofacial Surgery, Peking University School of Stomatology, Beijing 100081, China
01.09.2003
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ISSN | 0366-6999 2542-5641 |
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Abstract | Objective To investigate the effects in vitro of 17β-estradiol ( E2 ) on the proliferation and metabolism of rabbit mandibular condylar cartilage cells.Methods Chondrocytes were derived from neonatal rabbit mandibular condylar cartilage using a modified enzyme method. 17β-estradiol was added to the culture medium in a variety of concentrations. Cell growth and DNA, collagen, and proteoglycan synthesis were used as indicators of proliferation and differentiation of condylar chondrocytes. These were measured by cell number, ^3 H-proline and ^35S-incorporation, respectively.Results E2 increased cell number and ^3H-thymidine incorporation at 10^-8 to 10^-10mol/L, and 10^-8 to 10^-11 mol/L in a dose-dependent manner, peaking at 10^-8 mol/L and 10^-9mol/L, respectively.However, further increase in the concentration of estradiol caused inhibition of both cell number and ^3H-thymidine incorporation, and this was significant at 10^-6mol/L. The effect of E2 on proteglycan synthesis was similar; the maximum stimulating effect was at 10^-8mol/L, and inhibition was significant at 10^-6mol/L. There was no obvious stimulatory effect of E2 on ^3H-thymidine incorporation observed.Conclusions Estradiol affects condylar chondrocyte cell growth, DNA, and proteoglycan synthesis in a biphasic manner depending on its concentration. This indicates that estrogen may be important in the proliferation and differentiation of mandibular condylar chondrocytes, and could be relevant to some aspects of certain tempormandibular joint diseases by modulating the function of the chondrocytes. |
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AbstractList | To investigate the effects in vitro of 17 beta-estradiol (E2) on the proliferation and metabolism of rabbit mandibular condylar cartilage cells.
Chondrocytes were derived from neonatal rabbit mandibular condylar cartilage using a modified enzyme method. 17 beta-estradiol was added to the culture medium in a variety of concentrations. Cell growth and DNA, collagen, and proteoglycan synthesis were used as indicators of proliferation and differentiation of condylar chondrocytes. These were measured by cell number, 3H-proline and 35S-incorporation, respectively.
E2 increased cell number and 3H-thymidine incorporation at 10(-8) to 10(-10) mol/L, and 10(-8) to 10(-11) mol/L in a dose-dependent manner, peaking at 10(-8) mol/L and 10(-9) mol/L, respectively. However, further increase in the concentration of estradiol caused inhibition of both cell number and 3H-thymidine incorporation, and this was significant at 10(-6) mol/L. The effect of E2 on proteoglycan synthesis was similar; the maximum stimulating effect was at 10(-8) mol/L, and inhibition was significant at 10(-6) mol/L. There was no obvious stimulatory effect of E2 on 3H-thymidine incorporation observed.
Estradiol affects condylar chondrocyte cell growth, DNA, and proteoglycan synthesis in a biphasic manner depending on its concentration. This indicates that estrogen may be important in the proliferation and differentiation of mandibular condylar chondrocytes, and could be relevant to some aspects of certain temporomandibular joint diseases by modulating the function of the chondrocytes. Objective To investigate the effects in vitro of 17β-estradiol ( E2 ) on the proliferation and metabolism of rabbit mandibular condylar cartilage cells.Methods Chondrocytes were derived from neonatal rabbit mandibular condylar cartilage using a modified enzyme method. 17β-estradiol was added to the culture medium in a variety of concentrations. Cell growth and DNA, collagen, and proteoglycan synthesis were used as indicators of proliferation and differentiation of condylar chondrocytes. These were measured by cell number, ^3 H-proline and ^35S-incorporation, respectively.Results E2 increased cell number and ^3H-thymidine incorporation at 10^-8 to 10^-10mol/L, and 10^-8 to 10^-11 mol/L in a dose-dependent manner, peaking at 10^-8 mol/L and 10^-9mol/L, respectively.However, further increase in the concentration of estradiol caused inhibition of both cell number and ^3H-thymidine incorporation, and this was significant at 10^-6mol/L. The effect of E2 on proteglycan synthesis was similar; the maximum stimulating effect was at 10^-8mol/L, and inhibition was significant at 10^-6mol/L. There was no obvious stimulatory effect of E2 on ^3H-thymidine incorporation observed.Conclusions Estradiol affects condylar chondrocyte cell growth, DNA, and proteoglycan synthesis in a biphasic manner depending on its concentration. This indicates that estrogen may be important in the proliferation and differentiation of mandibular condylar chondrocytes, and could be relevant to some aspects of certain tempormandibular joint diseases by modulating the function of the chondrocytes. R5; Objective To investigate the effects in vitro of 17 β-estradiol (E2) on the proliferation and metabolism of rabbit mandibular condylar cartilage cells.Methods Chondrocytes were derived from neonatal rabbit mandibular condylar cartilage using a modified enzyme method. 17β-estradiol was added to the culture medium in a variety of concentrations. Cell growth and DNA, collagen, and proteoglycan synthesis were used as indicators of proliferation and differentiation of condylar chondrocytes. These were measured by cell number, 3H-proline and 35S-incorporation, respectively.Results E2 increased cell number and 3H-thymidine incorporation at 10-8 to 10-10 mol/L, and 10-8 to 10-11 mol/L in a dose-dependent manner, peaking at 10-8 mol/L and 10-9 mol/L, respectively. However, further increase in the concentration of estradiol caused inhibition of both cell number and 3H-thymidine incorporation, and this was significant at 10-6 mol/L. The effect of E2 on proteglycan synthesis was similar; the maximum stimulating effect was at 10-8 mol/L, and inhibition was significant at 10-6 mol/L. There was no obvious stimulatory effect of E2 on 3H-thymidine incorporation observed.Conclusions Estradiol affects condylar chondrocyte cell growth, DNA, and proteoglycan synthesis in a biphasic manner depending on its concentration. This indicates that estrogen may be important in the proliferation and differentiation of mandibular condylar chondrocytes, and could be relevant to some aspects of certain tempormandibular joint diseases by modulating the function of the chondrocytes. To investigate the effects in vitro of 17 beta-estradiol (E2) on the proliferation and metabolism of rabbit mandibular condylar cartilage cells.OBJECTIVETo investigate the effects in vitro of 17 beta-estradiol (E2) on the proliferation and metabolism of rabbit mandibular condylar cartilage cells.Chondrocytes were derived from neonatal rabbit mandibular condylar cartilage using a modified enzyme method. 17 beta-estradiol was added to the culture medium in a variety of concentrations. Cell growth and DNA, collagen, and proteoglycan synthesis were used as indicators of proliferation and differentiation of condylar chondrocytes. These were measured by cell number, 3H-proline and 35S-incorporation, respectively.METHODSChondrocytes were derived from neonatal rabbit mandibular condylar cartilage using a modified enzyme method. 17 beta-estradiol was added to the culture medium in a variety of concentrations. Cell growth and DNA, collagen, and proteoglycan synthesis were used as indicators of proliferation and differentiation of condylar chondrocytes. These were measured by cell number, 3H-proline and 35S-incorporation, respectively.E2 increased cell number and 3H-thymidine incorporation at 10(-8) to 10(-10) mol/L, and 10(-8) to 10(-11) mol/L in a dose-dependent manner, peaking at 10(-8) mol/L and 10(-9) mol/L, respectively. However, further increase in the concentration of estradiol caused inhibition of both cell number and 3H-thymidine incorporation, and this was significant at 10(-6) mol/L. The effect of E2 on proteoglycan synthesis was similar; the maximum stimulating effect was at 10(-8) mol/L, and inhibition was significant at 10(-6) mol/L. There was no obvious stimulatory effect of E2 on 3H-thymidine incorporation observed.RESULTSE2 increased cell number and 3H-thymidine incorporation at 10(-8) to 10(-10) mol/L, and 10(-8) to 10(-11) mol/L in a dose-dependent manner, peaking at 10(-8) mol/L and 10(-9) mol/L, respectively. However, further increase in the concentration of estradiol caused inhibition of both cell number and 3H-thymidine incorporation, and this was significant at 10(-6) mol/L. The effect of E2 on proteoglycan synthesis was similar; the maximum stimulating effect was at 10(-8) mol/L, and inhibition was significant at 10(-6) mol/L. There was no obvious stimulatory effect of E2 on 3H-thymidine incorporation observed.Estradiol affects condylar chondrocyte cell growth, DNA, and proteoglycan synthesis in a biphasic manner depending on its concentration. This indicates that estrogen may be important in the proliferation and differentiation of mandibular condylar chondrocytes, and could be relevant to some aspects of certain temporomandibular joint diseases by modulating the function of the chondrocytes.CONCLUSIONSEstradiol affects condylar chondrocyte cell growth, DNA, and proteoglycan synthesis in a biphasic manner depending on its concentration. This indicates that estrogen may be important in the proliferation and differentiation of mandibular condylar chondrocytes, and could be relevant to some aspects of certain temporomandibular joint diseases by modulating the function of the chondrocytes. |
Author | 程鹏 马绪臣 薛延 李盛琳 张祖燕 |
AuthorAffiliation | CenterforTemporomandibularDisorders,PekingUniversitySchoolofStomatology,Beijing100081,China LaboratoryofMolecularBiology,BeijingJishuitanHospital,Beijing100083,China LaboratoryofOralandMaxillofacialSurgery,PekingUniversitySchoolofStomatology,Beijing100081,China |
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Snippet | Objective To investigate the effects in vitro of 17β-estradiol ( E2 ) on the proliferation and metabolism of rabbit mandibular condylar cartilage cells.Methods... To investigate the effects in vitro of 17 beta-estradiol (E2) on the proliferation and metabolism of rabbit mandibular condylar cartilage cells. Chondrocytes... To investigate the effects in vitro of 17 beta-estradiol (E2) on the proliferation and metabolism of rabbit mandibular condylar cartilage cells.OBJECTIVETo... R5; Objective To investigate the effects in vitro of 17 β-estradiol (E2) on the proliferation and metabolism of rabbit mandibular condylar cartilage... |
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SubjectTerms | Animals Cartilage, Articular - cytology Cartilage, Articular - metabolism Cell Differentiation Cell Division - drug effects Cells, Cultured Estradiol - pharmacology Mandibular Condyle - cytology Mandibular Condyle - metabolism Rabbits 细胞增殖 软骨细胞 雌二醇 髁关节 |
Title | Effects of estradiol on proliferation and metabolism of rabbit mandibular condylar cartilage cells in vitro |
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