Zuscik M J, Gunter T E, Rosier R N, Gunter K K, Puzas J E
Department of Orthopaedics, University of Rochester School of Medicine and Dentistry, New York.
Cell Calcium. 1994 Aug;16(2):112-22. doi: 10.1016/0143-4160(94)90006-x.
Parathyroid hormone (PTH) is one of the most potent stimulators of growth plate chondrocyte mitogenesis that has been reported. However, study of the second messenger signaling mechanisms involved in the transduction of the hormone's effects on these cells is incomplete. Our data indicate that in addition to stimulating cyclic adenosine-3'5'-monophosphate metabolism, PTH also activates the phosphoinositide cascade, the pathway responsible for the generation of inositol-1,4,5-trisphosphate dependent Ca2+ signals. Our conclusion that PTH activates the phosphoinositide cascade is based on data that demonstrate: (1) the Ca2+ transients evoked by the hormone are dependent on intracellular Ca2+ stores; (2) the hormone stimulates the release of radiolabeled inositol from GPC plasma membranes; and (3) the hormone stimulates a greater than 8-fold increase in cytosolic inositol-1,4,5-trisphosphate pool size.
甲状旁腺激素(PTH)是已报道的对生长板软骨细胞有丝分裂最有效的刺激物之一。然而,关于该激素对这些细胞作用转导过程中涉及的第二信使信号传导机制的研究尚不完整。我们的数据表明,除了刺激环磷酸腺苷(cAMP)代谢外,PTH还激活磷脂酰肌醇级联反应,该途径负责生成依赖于肌醇-1,4,5-三磷酸(IP3)的钙离子信号。我们关于PTH激活磷脂酰肌醇级联反应的结论基于以下数据:(1)该激素诱发的钙离子瞬变依赖于细胞内钙离子储存;(2)该激素刺激从甘油磷脂酰胆碱(GPC)质膜释放放射性标记的肌醇;(3)该激素刺激胞质肌醇-1,4,5-三磷酸池大小增加超过8倍。