Eliam M C, Baslé M, Bouizar Z, Bielakoff J, Moukhtar M, de Vernejoul M C
INSERM U18, Hôpital Lariboisière, Paris, France.
J Endocrinol. 1988 Nov;119(2):243-8. doi: 10.1677/joe.0.1190243.
Isolated osteoclasts obtained from young chickens fed a normal (+Ca) or deficient (-Ca) calcium and vitamin D diet for 3 weeks, were studied for their ability to bind salmon calcitonin (sCT). Osteoclasts obtained from -Ca chickens, when incubated with 0.1 mumol sCT/l, doubled cyclic (c)AMP production and retracted from a glass support, as observed by scanning electron microscopy. The presence of receptors was also demonstrated by autoradiography and competition analysis of 125I-labelled sCT binding. The number of receptors per cell was 0.9 +/- 0.1 x 10(4). In contrast, osteoclasts obtained from +Ca chickens did not increase cAMP production and did not retract in the presence of 0.1 mumol sCT/l. No specific binding of 125I-labelled sCT could be demonstrated on these osteoclasts. Plasma levels of calcium and calcitonin were measured in +Ca and -Ca chickens. The plasma concentration of calcium was markedly lower at 3 weeks in -Ca than in +Ca chickens. The plasma concentration of calcitonin was decreased in -Ca chickens compared with +Ca chickens at the first week and kept decreasing during the 3 weeks. These results strongly support the hypothesis that calcium and vitamin D intake regulate plasma calcitonin levels in chickens, and that calcitonin receptors can be detected on chicken osteoclasts only when blood calcium is decreased by a diet deficient in calcium and vitamin D.
从食用正常(+Ca)或缺乏(-Ca)钙和维生素D饮食3周的幼鸡中分离出破骨细胞,研究其结合鲑鱼降钙素(sCT)的能力。如通过扫描电子显微镜观察到的,当与0.1μmol sCT / l一起孵育时,从-Ca鸡获得的破骨细胞使环(c)AMP产量增加一倍,并从玻璃支持物上缩回。放射自显影和125I标记的sCT结合的竞争分析也证明了受体的存在。每个细胞的受体数量为0.9 +/- 0.1 x 10(4)。相比之下,从+Ca鸡获得的破骨细胞在存在0.1μmol sCT / l的情况下不会增加cAMP产量,也不会缩回。在这些破骨细胞上未显示125I标记的sCT的特异性结合。测量了+Ca和-Ca鸡的血浆钙和降钙素水平。在3周时,-Ca鸡的血浆钙浓度明显低于+Ca鸡。与+Ca鸡相比,-Ca鸡在第一周时血浆降钙素浓度降低,并在3周内持续下降。这些结果有力地支持了以下假设:钙和维生素D的摄入量调节鸡的血浆降钙素水平,并且只有当饮食中钙和维生素D缺乏导致血钙降低时,才能在鸡破骨细胞上检测到降钙素受体。