首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Effects of calcitonin and parathyroid hormone on calcification of primary cultures of chicken growth plate chondrocytes.
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Effects of calcitonin and parathyroid hormone on calcification of primary cultures of chicken growth plate chondrocytes.

机译:降钙素和甲状旁腺激素对鸡生长板软骨细胞原代培养钙化的影响。

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Few studies have been directed toward elucidating the action of calcitonin (CT) and parathyroid hormone (PTH) on growth plate chondrocytes, cells directly involved in longitudinal bone growth and provisional calcification. In this study, primary cultures of avian growth plate chondrocytes that calcify without the supplement of beta-glycerophosphate were used to investigate the effects of synthetic human CT and 1-34 bovine PTH on (1) cell division and growth; (2) the deposition of Ca2+ and inorganic phosphate (Pi); (3) the activity of alkaline phosphatase (AP), an enzyme long associated with the mineralization process; (4) the levels of proteoglycans; and (5) the synthesis of collagens. Added continually to preconfluent cultures from day 6 until harvest, CT (1-30 nM) and PTH (0.1-1.0 nM) increased mineral deposition; the maximal increase was seen between days 18-21 at 10 nM CT (175-260%) and 0.5 nM PTH (approximately 170-280%), both p < 0.001. CT had no significant effect on cellular protein, or AP-specific activity, whereas PTH increased cellular protein, DNA, proteoglycan, and collagen content of the cultures in a dosage-dependent manner. AP activity and levels of Type II and X collagens and fibronectin in the culture medium showed a biphasic response to PTH; maximal increases were seen at 0.5 nM between days 15-18. Longer exposure (days 21-27) to PTH at higher levels (5-10 nM) caused a marked decreased in AP activity but a lesser decrease in the collagens. These results indicate that CT and PTH can act directly on chondrocytes to stimulate mineralization, but that PTH specifically stimulated cell division and synthesis of cellular and extracellular proteins by growth plate chondrocytes. The implications of these findings with regard to Ca2+ homeostasis and bone formation are discussed.
机译:很少有研究阐明降钙素(CT)和甲状旁腺激素(PTH)对生长板软骨细胞,直接参与纵向骨生长和临时钙化的细胞的作用。在这项研究中,不添加β-甘油磷酸钙化的禽生长板软骨细胞的原代培养被用于研究合成人CT和1-34牛PTH对(1)细胞分裂和生长的影响。 (2)Ca2 +和无机磷酸盐(Pi)的沉积; (3)碱性磷酸酶(AP)的活性,一种与矿化过程长期相关的酶; (4)蛋白聚糖的水平; (5)胶原蛋白的合成。从第6天到收获前连续添加到融合前的培养物中,CT(1-30 nM)和PTH(0.1-1.0 nM)增加了矿物质沉积;在18 n至21天之间在10 nM CT(175-260%)和0.5 nM PTH(约170-280%)之间观察到最大的增加,两者均p <0.001。 CT对细胞蛋白或AP特异性活性无明显影响,而PTH以剂量依赖性方式增加培养物中细胞蛋白,DNA,蛋白聚糖和胶原蛋白含量。培养基中的AP活性和II型和X型胶原蛋白和纤连蛋白的水平显示出对PTH的双相反应。在第15至18天之间,在0.5 nM处观察到最大增加。较高水平(5-10 nM)的PTH暴露时间较长(第21-27天)会导致AP活性明显下降,但胶原蛋白的下降幅度较小。这些结果表明,CT和PTH可以直接作用于软骨细胞以刺激矿化,但是PTH特异性地刺激细胞分裂以及生长板软骨细胞对细胞和细胞外蛋白的合成。讨论了这些发现对Ca2 +稳态和骨形成的影响。

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