McSheehy P M, Chambers T J
Endocrinology. 1986 Oct;119(4):1654-9. doi: 10.1210/endo-119-4-1654.
PTH stimulates osteoclastic bone resorption in vivo and in organ culture. We have previously found that if osteoclasts are disaggregated from bone and incubated on bone slices, PTH does not increase bone resorption, but does so if osteoblastic cells are added to the cultures. This suggests that PTH acts primarily on osteoblasts, which are induced by the presence of the hormone to stimulate osteoclastic bone resorption. In the present paper we describe investigations into the mechanism by which osteoblastic cells stimulate osteoclasts. We found that increased resorption could not be accounted for by changes in the bone substrate. Osteoblast-like cells (UMR106) incubated with PTH did, however, release a factor into the culture supernatant that stimulated osteoclastic bone resorption. This factor was stable for at least 7 days when stored at 4 C and survived freeze-thawing, but was inactivated by heating to 65 C for 30 min. Activity was lost entirely after dialysis using a Spectrapor membrane with a mol wt cut-off (MWCO) of 2000. The small size of the molecule was confirmed after ultrafiltration across Amicon filters YM2 and YC05. There was no loss of activity across YM2 (MWCO, 1000), but, in contrast, there was no stimulation in the conditioned medium after ultrafiltration across YC05 (MWCO, 500).
甲状旁腺激素(PTH)在体内和器官培养中均可刺激破骨细胞介导的骨吸收。我们之前发现,如果将破骨细胞从骨组织中分离出来并接种于骨切片上进行培养,PTH并不会增加骨吸收;但是,如果在培养体系中加入成骨细胞,PTH则可促进骨吸收。这表明,PTH主要作用于成骨细胞,激素的存在可诱导成骨细胞刺激破骨细胞介导的骨吸收。在本文中,我们描述了对成骨细胞刺激破骨细胞机制的研究。我们发现,骨吸收增加不能用骨底物的变化来解释。然而,与PTH共同孵育的成骨样细胞(UMR106)可向培养上清中释放一种刺激破骨细胞介导骨吸收的因子。该因子于4℃保存至少7天仍保持稳定,且冻融后活性依然存在,但经65℃加热30分钟即被灭活。使用截留分子量(MWCO)为2000的Spectrapor膜进行透析后,活性完全丧失。经Amicon YM2和YC05滤膜超滤后证实该分子体积较小。经YM2(MWCO,1000)超滤后活性无损失,但相反,经YC05(MWCO,500)超滤后的条件培养基则无刺激活性。