Schneider H G, Raue F, Bollenbach N, Scherübl H, Ziegler R
Department of Internal Medicine I, University of Heidelberg, FRG.
Acta Endocrinol (Copenh). 1990 Feb;122(2):255-62. doi: 10.1530/acta.0.1220255.
Cultured rat kidney cells possess specific calcitonin receptors and a calcitonin-responsive adenylate cyclase. At 37 degrees C bound 125I-salmon calcitonin becomes increasingly resistant to acid washing. If 125I-salmon calcitonin is removed from the medium after binding, bound hormone decreases over the next 5 h. Monensin, which blocks lysosomal processing, inhibits the decrease of bound hormone. These data indicate that calcitonin receptors are internalized after binding of hormone in kidney cells. Cycloheximide prevents internalization, when it is administered 4 h before 125I-salmon calcitonin binding is studied. Pre-incubation of the cells with 10(-7) mol/l unlabelled salmon calcitonin decreases specific binding; recovery of binding needs 48 h to occur. The long time interval for recovery makes it unlikely that calcitonin receptors recycle. This is the first demonstration that normal rat kidney cells internalize calcitonin after binding. It might contribute to the loss of calcitonin bioactivity which is seen after continuous administration.
培养的大鼠肾细胞具有特异性降钙素受体和降钙素反应性腺苷酸环化酶。在37摄氏度时,结合的125I-鲑鱼降钙素对酸洗的抗性越来越强。如果在结合后将125I-鲑鱼降钙素从培养基中去除,结合的激素在接下来的5小时内会减少。莫能菌素可阻断溶酶体加工过程,抑制结合激素的减少。这些数据表明,在肾细胞中激素结合后降钙素受体会被内化。当在研究125I-鲑鱼降钙素结合前4小时给予放线菌酮时,它可阻止内化。用10(-7)mol/l未标记的鲑鱼降钙素对细胞进行预孵育会降低特异性结合;结合的恢复需要48小时才能发生。恢复所需的长时间间隔使得降钙素受体不太可能循环利用。这是首次证明正常大鼠肾细胞在结合后会内化降钙素。这可能导致连续给药后出现的降钙素生物活性丧失。