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甲状旁腺激素、秋水仙碱和降钙素对器官培养中破骨细胞超微结构及活性的影响。

The effects of parathyroid hormone, colchicine, and calcitonin on the ultrastructure and the activity of osteoclasts in organ culture.

作者信息

Holtrop M E, Raisz L G, Simmons H A

出版信息

J Cell Biol. 1974 Feb;60(2):346-55. doi: 10.1083/jcb.60.2.346.

Abstract

The ultrastructure of osteoclasts was examined in fetal rat bones after stimulation or inhibition of resorption in culture. A central ruffled border area completely encircled by a clear zone was considered to represent the resorbing system of the cell. The proportion of ruffled border and clear zone in osteoclast cross sections was compared with changes in bone resorption as measured by the release of previously incorporated radioactive calcium ((45)Ca). In control cultures 55% of the osteoclast cross sections showed an area closely apposed to bone and this consisted mainly of clear zone; only 11% showed ruffled borders. Treatment with parathyroid hormone (PTH) increased (45)Ca release, increased the frequency of finding areas closely apposed to bone (79%), and markedly increased the frequency of the ruffled border area (64%). Colchicine given concurrently with PTH decreased the number of osteoclasts. Colchicine or calcitonin treatment after PTH stimulation decreased the proportion of ruffled border area significantly by 1 h; this was followed by a decrease in (45)Ca release. These inhibited osteoclasts resembled osteoclasts from control, unstimulated cultures, suggesting that the cells had returned to their inactive state. Colchicine-treated osteoclasts also showed a loss of microtubules and a massive accumulation of 100 A filaments, suggesting that synthesis of microtubular subunits had increased.

摘要

在培养中对胎鼠骨骼进行吸收刺激或抑制后,对破骨细胞的超微结构进行了检查。一个由透明区完全环绕的中央皱襞缘区域被认为代表了细胞的吸收系统。将破骨细胞横截面中皱襞缘和透明区的比例与通过先前掺入的放射性钙(45Ca)释放量测量的骨吸收变化进行了比较。在对照培养物中,55%的破骨细胞横截面显示有一个与骨紧密相邻的区域,这主要由透明区组成;只有11%显示有皱襞缘。用甲状旁腺激素(PTH)处理可增加45Ca释放量,增加发现与骨紧密相邻区域的频率(79%),并显著增加皱襞缘区域的频率(64%)。与PTH同时给予秋水仙碱可减少破骨细胞数量。在PTH刺激后给予秋水仙碱或降钙素,1小时后皱襞缘区域的比例显著降低;随后45Ca释放量减少。这些受抑制的破骨细胞类似于来自未受刺激的对照培养物中的破骨细胞,表明细胞已恢复到非活性状态。用秋水仙碱处理的破骨细胞还显示微管丢失和100埃细丝大量积累,表明微管亚基的合成增加。

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