Krieger N S
Department of Medicine, University of Rochester, New York.
J Bone Miner Res. 1992 Sep;7(9):1105-11. doi: 10.1002/jbmr.5650070914.
Based on the inhibition of stimulated Ca release from cultured bone by several different agents that alter Na transport, we proposed that hormonally stimulated bone resorption requires Na/Ca exchange. Calcemic hormones appear to interact primarily directly with the osteoblast, which then mediates the activation of osteoclast activity. In organ culture it is not possible to determine whether Na/Ca exchange is involved in this initiating step in the osteoblast or directly in osteoclast-mediated Ca release, and there have been no prior direct measurements of Na/Ca exchange in bone or bone cells. The purpose of this study was to demonstrate the presence of Na/Ca exchange transport in the osteoblast. Thus, we characterized Na-dependent Ca transport in osteoblast-like rat osteosarcoma cells (UMR-106) and primary bone cells isolated from neonatal mouse calvaria. Cells were loaded with the Ca-sensitive dye fura-2 in the presence of physiologic NaCl and the absence of Ca with or without 0.3 mM ouabain. Changes in free cytosolic Ca after the extracellular addition of 1.5 mM Ca were measured spectrofluorimetrically. An outward Na gradient was generated by decreasing extracellular Na while maintaining isotonicity. UMR-106 cells that were Na loaded by ouabain inhibition of Na,K-ATPase activity exhibited 30% greater Ca uptake than control cells. Similar results were obtained with primary bone cells. This uptake required extracellular Ca, was not inhibited by 200 microM verapamil, and was reversible upon reversal of the Na gradient. These data demonstrate the presence of a Na/Ca exchange transport system in osteoblasts.
基于几种改变钠转运的不同试剂对培养骨中刺激的钙释放的抑制作用,我们提出激素刺激的骨吸收需要钠/钙交换。降钙素似乎主要直接与成骨细胞相互作用,然后介导破骨细胞活性的激活。在器官培养中,无法确定钠/钙交换是参与成骨细胞的这一起始步骤,还是直接参与破骨细胞介导的钙释放,并且此前没有对骨或骨细胞中的钠/钙交换进行过直接测量。本研究的目的是证明成骨细胞中存在钠/钙交换转运。因此,我们对大鼠成骨肉瘤细胞(UMR-106)和从新生小鼠颅骨分离的原代骨细胞中依赖钠的钙转运进行了表征。在生理氯化钠存在且无钙的情况下,加入或不加入0.3 mM哇巴因,用钙敏感染料fura-2加载细胞。在细胞外添加1.5 mM钙后,用荧光分光光度法测量游离胞质钙的变化。通过降低细胞外钠同时保持等渗性来产生外向钠梯度。通过哇巴因抑制钠钾ATP酶活性加载钠的UMR-106细胞比对照细胞表现出高30%的钙摄取。原代骨细胞也得到了类似的结果。这种摄取需要细胞外钙,不受200 microM维拉帕米的抑制,并且在钠梯度反转时是可逆的。这些数据证明成骨细胞中存在钠/钙交换转运系统。