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...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. 17p-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.展开更多
文摘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. 17p-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.
