Schanne F A, Dowd T L, Gupta R K, Rosen J F
Department of Pediatrics, Albert Einstein College of Medicine, Bronx, NY 10461.
Proc Natl Acad Sci U S A. 1989 Jul;86(13):5133-5. doi: 10.1073/pnas.86.13.5133.
Lead (Pb) has been shown to perturb Ca-mediated cellular processes. However, to date, a direct effect of Pb on intracellular free Ca2+ concentration ([Ca2+]i) has not been demonstrated. 19F NMR in combination with 1,2-bis(2-amino-5-fluorophenoxy)ethane-N,N,N',N'-tetraacetic acid (5F-BAPTA) was used to simultaneously measure [Ca2+]i and intracellular free Pb2+ concentration ([Pb2+]i) in the rat osteoblastic bone cell line ROS 17/2.8. The basal concentration of [Ca2+]i in ROS 17/2.8 cells was measured to be 128 +/- 24 nM. Treatment with Pb2+ at 5 and 25 microM produced sustained 50% and 120% increases in [Ca2+]i, respectively, over a time course of 5 hr. At a medium Pb2+ concentration of 25 microM, the entry of Pb2+ into ROS 17/2.8 cells yielded measurable [Pb2+]i in cultured cells. Collectively, these findings advance the hypothesis that Pb toxicity is mediated, in part, through perturbations in [Ca2+]i.
铅(Pb)已被证明会干扰钙介导的细胞过程。然而,迄今为止,尚未证实铅对细胞内游离钙离子浓度([Ca2+]i)有直接影响。19F核磁共振结合1,2-双(2-氨基-5-氟苯氧基)乙烷-N,N,N',N'-四乙酸(5F-BAPTA)用于同时测量大鼠成骨细胞系ROS 17/2.8中的[Ca2+]i和细胞内游离铅离子浓度([Pb2+]i)。测得ROS 17/2.8细胞中[Ca2+]i的基础浓度为128±24 nM。在5小时的时间进程中,用5 microM和25 microM的Pb2+处理分别使[Ca2+]i持续增加50%和120%。在25 microM的中等Pb2+浓度下,Pb2+进入ROS 17/2.8细胞导致培养细胞中可测量的[Pb2+]i。总体而言,这些发现支持了铅毒性部分是通过[Ca2+]i的扰动介导的这一假设。