Raisz L G, Luben R A, Mundy G R, Dietrich J W, Horton J E, Trummel C L
J Clin Invest. 1975 Aug;56(2):408-13. doi: 10.1172/JCI108106.
The effects of osteoclast activating factor (OAF) released by normal human peripheral blood leukocytes cultured with phytohemagglutinin have been examined in organ culture. Like parathyroid hormone (PTH), OAF causes a rapid increased in the release of previously incorporated 45Ca from fetal rat bone after brief or continuous exposure; the bones also lose stable calcium and collagen content. The resorption response to OAF also resembles that of PTH in having a steep dose response curve and being only transiently inhibited by calcitonin and partially inhibited by increasing medium phosphate concentration. OAF-stimulated resorption was inhibited more effectively by cortisol than was PTH stimulation. The response to maximally effective doses of OAF was not enhanced by PTH or prostaglandin E2, but submaximal doses gave additive effects. Both OAF and PTH inhibit collagen synthesis in fetal rat calvaria at the concentrations that stimulate bone resorption.
在用植物血凝素培养的正常人外周血白细胞释放的破骨细胞激活因子(OAF)的作用已在器官培养中进行了研究。与甲状旁腺激素(PTH)一样,OAF在短暂或持续暴露后会导致胎鼠骨中先前掺入的45Ca释放迅速增加;骨骼还会失去稳定的钙和胶原蛋白含量。对OAF的吸收反应也与PTH相似,具有陡峭的剂量反应曲线,仅被降钙素短暂抑制,并被增加培养基磷酸盐浓度部分抑制。皮质醇比PTH刺激更有效地抑制OAF刺激的吸收。PTH或前列腺素E2不会增强对最大有效剂量OAF的反应,但次最大剂量会产生相加作用。在刺激骨吸收的浓度下,OAF和PTH都会抑制胎鼠颅骨中的胶原蛋白合成。