Merke J, Klaus G, Hügel U, Waldherr R, Ritz E
J Clin Invest. 1986 Jan;77(1):312-4. doi: 10.1172/JCI112292.
1,25-dihydroxyvitamin D3 (1,25(OH)2D3) is known to stimulate osteoclastic bone resorption in vivo and whole organ bone culture systems in vitro. It has not been established whether 1,25(OH)2D3 acts directly on osteoclasts or whether its action on osteoclasts is mediated via other bone cells (e.g., osteoblasts) or recruitment of osteoclast precursor cells. Circulating monocytes have been characterized as osteoclast precursors. In the present study, vitamin D3-replete chicken on a calcium-deficient diet were studied. Circulating monocytes, whole bone cell preparations, and isolated osteoclasts (differential sedimentation) were examined for presence of 1,25(OH)2D3 receptors. Reversible, specific, and saturable binding of [3H]-1,25(OH)2D3 to a 3.5 S macromolecule was demonstrated in nuclear fractions of monocytes (maximal binding capacity, 48 fmol/mg protein; dissociation constant, 1.3 X 10(-10) M) and of whole bone cell preparations. 1,25(OH)2D3 receptors were not demonstrable in osteoclast preparations (70% pure; detection threshold, 2 fmol/mg protein). Data are consistent with indirect action of 1,25(OH)2D3 on osteoclastic bone resorption.
已知1,25 - 二羟基维生素D3(1,25(OH)2D3)在体内可刺激破骨细胞介导的骨吸收,在体外全器官骨培养系统中也有此作用。目前尚不清楚1,25(OH)2D3是直接作用于破骨细胞,还是其对破骨细胞的作用是通过其他骨细胞(如成骨细胞)介导,抑或是通过募集破骨细胞前体细胞来实现。循环单核细胞已被确认为破骨细胞前体。在本研究中,对食用缺钙日粮的维生素D3充足的鸡进行了研究。检测了循环单核细胞、全骨细胞制剂和分离的破骨细胞(差异沉降法)中1,25(OH)2D3受体的存在情况。在单核细胞的核组分以及全骨细胞制剂中,证实了[3H]-1,25(OH)2D3与一种3.5S大分子存在可逆、特异性和可饱和的结合(最大结合容量为48 fmol/mg蛋白;解离常数为1.3×10(-10)M)。在破骨细胞制剂(纯度70%;检测阈值为2 fmol/mg蛋白)中未检测到1,25(OH)2D3受体。这些数据与1,25(OH)2D3对破骨细胞介导的骨吸收的间接作用一致。