Niu Katelyn Y, Noyes Nathaniel C, Abrams Thomas W
Department of Pharmacology, University of Maryland School of Medicine, 655 West Baltimore Street, Baltimore, MD 21201-1559, USA.
J Pharmacol Toxicol Methods. 2012 May-Jun;65(3):122-5. doi: 10.1016/j.vascn.2012.03.005. Epub 2012 Apr 6.
Lead exposure can cause learning disabilities, memory loss and severe damage to the nervous system. However, the exact mechanism by which lead causes learning disabilities is not fully understood. The effects of lead on calcium-regulated signaling pathways are difficult to study biochemically; with the traditional method of controlling the free calcium concentration with EGTA, the exact concentrations of free lead and calcium ions in solution are interdependent and prone to error because EGTA also buffers lead.
In our approach, we first reduced the free calcium concentration in the solution using calcium-binding resins before adding lead to buffers. The solution was sequentially treated with Chelex-100 ion exchange resin, followed by immobilized BAPTA resin. The final concentration of free calcium in the solution was measured with Fluo-3 indicator. Our protocol successfully produced buffers with free calcium levels below 15 nM, which is substantially below threshold for activation of calcium-dependent enzymes in signaling pathways (which is typically a few hundred nanomolar calcium, when determined in vitro).
This method provides an improved approach to study the effect of heavy metals on calcium-stimulated signaling pathways.
铅暴露可导致学习障碍、记忆力减退以及对神经系统的严重损害。然而,铅导致学习障碍的确切机制尚未完全明确。铅对钙调节信号通路的影响难以通过生物化学方法进行研究;使用EGTA控制游离钙浓度的传统方法中,溶液中游离铅和钙离子的确切浓度相互依存且容易出错,因为EGTA也会螯合铅。
在我们的方法中,在向缓冲液中添加铅之前,我们首先使用钙结合树脂降低溶液中的游离钙浓度。溶液依次用Chelex-100离子交换树脂处理,然后用固定化BAPTA树脂处理。用Fluo-3指示剂测量溶液中游离钙的最终浓度。我们的方案成功制备出游离钙水平低于15 nM的缓冲液,这大大低于信号通路中钙依赖性酶激活的阈值(体外测定时,通常为几百纳摩尔钙)。
该方法为研究重金属对钙刺激信号通路的影响提供了一种改进的方法。