Nygren P, Larsson R, Johansson H, Ljunghall S, Rastad J, Akerström G
Department of Medical Cell Biology, University of Uppsala, Sweden.
Calcif Tissue Int. 1988 Oct;43(4):213-8. doi: 10.1007/BF02555137.
Increasing the extracellular Ca2+ concentration from 0.5 to 3.0 mM induced marked increments in cytoplasmic Ca2+ concentration (Ca2+i) and inhibition of parathyroid hormone (PTH) release of freshly isolated bovine parathyroid cells. 1,25-dihydroxycholecalciferol (1,24(OH)2D3; 0.1-100 ng/ml) did not affect (Ca2+i) and was also without acute effect on the secretion. During 4 days of monolayer culture, the parathyroid cells underwent significant increases in both number and size, and presence of 10-100 ng/ml 1,25(OH)2D3 almost completely inhibited the cell proliferation, whereas the hypertrophy was unaffected. One day of culture with 0.1-100 ng/ml 1,25(OH)2D3 was without effect on PTH release but after 4 days there was a dose-related reduction of secretion. At this time point and irrespective of the culture condition, PTH release was no longer suppressed by high extracellular Ca2+. Furthermore, Ca2+i increased little upon increments in the extracellular Ca2+ concentration as compared with freshly isolated cells. It is concluded that after prolonged exposure to 1,25(OH)2D3, PTH release is inhibited and, at high concentrations, the parathyroid cells cease to proliferate. However, 1,25(OH)2D3 does not affect the development of functional dedifferentiation of parathyroid cells during monolayer culture.
将细胞外钙离子浓度从0.5 mM提高到3.0 mM可使新鲜分离的牛甲状旁腺细胞的细胞质钙离子浓度(Ca2+i)显著升高,并抑制甲状旁腺激素(PTH)释放。1,25-二羟胆钙化醇(1,25(OH)2D3;0.1 - 100 ng/ml)不影响(Ca2+i),对分泌也无急性影响。在单层培养的4天中,甲状旁腺细胞数量和大小均显著增加,10 - 100 ng/ml 1,25(OH)2D3的存在几乎完全抑制细胞增殖,而细胞肥大不受影响。用0.1 - 100 ng/ml 1,25(OH)2D3培养1天对PTH释放无影响,但4天后分泌出现剂量相关的减少。此时,无论培养条件如何,高细胞外钙离子不再抑制PTH释放。此外,与新鲜分离的细胞相比,细胞外钙离子浓度升高时Ca2+i增加很少。结论是,长时间暴露于1,25(OH)2D3后,PTH释放受到抑制,且在高浓度时甲状旁腺细胞停止增殖。然而,1,25(OH)2D3不影响单层培养期间甲状旁腺细胞功能性去分化的发展。