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Investigation of a Calcium-Responsive Contrast Agent in Cellular Model Systems: Feasibility for Use as a Smart Molecular Probe in Functional MRI

机译:细胞模型系统中钙响应性对比剂的研究:在功能性mRI中用作智能分子探针的可行性

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摘要

Responsive or smart contrast agents (SCAs) represent a promising direction for development of novel functional MRI (fMRI) methods for the eventual noninvasive assessment of brain function. In particular, SCAs that respond to Ca2+ may allow tracking neuronal activity independent of brain vasculature, thus avoiding the characteristic limitations of current fMRI techniques. Here we report an in vitro proof-of-principle study with a Ca2+-sensitive, Gd3+-based SCA in an attempt to validate its potential use as a functional in vivo marker. First, we quantified its relaxometric response in a complex 3D cell culture model. Subsequently, we examined potential changes in the functionality of primary glial cells following administration of this SCA. Monitoring intracellular Ca2+ showed that, despite a reduction in the Ca2+ level, transport of Ca2+ through the plasma membrane remained unaffected, while stimulation with ATP induced Ca2+-transients suggested normal cellular signaling in the presence of low millimolar SCA concentrations. SCAs merely lowered the intracellular Ca2+ level. Finally, we estimated the longitudinal relaxation times (T1) for an idealized in vivo fMRI experiment with SCA, for extracellular Ca2+ concentration level changes expected during intense neuronal activity which takes place upon repetitive stimulation. The values we obtained indicate changes in T1 of around 1ndash;6%, sufficient to be robustly detectable using modern MRI methods in high field scanners. Our results encourage further attempts to develop even more potent SCAs and appropriate fMRI protocols. This would result in novel methods that allow monitoring of essential physiological processes at the cellular and molecular level.
机译:响应式或智能对比剂(SCA)代表了一种新的功能性MRI(fMRI)方法的发展方向,该方法可用于最终的非侵入性脑功能评估。特别是,响应Ca2 +的SCA可以跟踪神经元的活动,而与大脑的脉管系统无关,从而避免了当前fMRI技术的特征局限性。在这里,我们报告了一项基于Ca2 +敏感,基于Gd3 +的SCA的体外原理验证研究,试图验证其作为功能性体内标记物的潜在用途。首先,我们在复杂的3D细胞培养模型中量化了其弛豫响应。随后,我们检查了这种SCA给药后原代神经胶质细胞功能的潜在变化。监测细胞内Ca2 +的结果显示,尽管Ca2 +含量降低,但Ca2 +通过质膜的转运仍然不受影响,而ATP诱导的Ca2 +瞬变刺激表明在低毫摩尔SCA浓度下正常的细胞信号传导。 SCA仅降低了细胞内Ca2 +水平。最后,我们估计了理想的SCA体内fMRI实验的纵向弛豫时间(T1),该弛豫时间是针对在重复刺激后发生的强烈神经元活动期间预期的细胞外Ca2 +浓度水平变化。我们获得的值表明T1的变化约为1%至6%,足以使用高场扫描仪中的现代MRI方法可靠地检测到。我们的结果鼓励进一步尝试开发更有效的SCA和合适的fMRI方案。这将导致新颖的方法,该方法允许在细胞和分子水平上监测基本的生理过程。

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