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一种新的金标准方法,用于描述动物细胞跨膜运输 Si 的特性。

A new gold standard approach to characterize the transport of Si across cell membranes in animals.

机构信息

The Nephrology Research Group, Department of Medicine, Laval University, Québec, Canada.

Cardiometabolic Research Group, Department of Kinesiology, University of Montréal, Montreal, Canada.

出版信息

J Cell Physiol. 2018 Oct;233(10):6369-6376. doi: 10.1002/jcp.26476. Epub 2018 Apr 18.

Abstract

Silicon (Si) is increasingly recognized as an essential trace element in animals, especially since the identification of mammalian Si transport systems and Si responsive genes not long ago. During many years, however, efforts to gain substantial insight into the biological role of this element in animals have achieved partial success due in part to the unavailability of validated protocols to study Si movement across biological membranes. To circumvent such limitations, we have developed a general transport assay in which cellular Si content was determined by automated electrothermal atomic absorption spectrophotometry. We have found this assay to provide great analytic sensitivity with Si detection thresholds of less than 1 µM, that is, below or very close to the concentration range of animal cells. We have also found this assay to provide valid and cost-effective determinations in Si transport studies while requiring workable quantities of samples. The protocol described here should thus become gold standard toward accelerated progress in the field of Si transport.

摘要

硅(Si)越来越被认为是动物必需的微量元素,尤其是在不久前鉴定出哺乳动物 Si 转运系统和 Si 响应基因之后。然而,多年来,由于缺乏有效的研究生物膜中 Si 迁移的验证方案,人们对该元素在动物中的生物学作用的深入了解仅取得了部分成功。为了克服这些限制,我们开发了一种通用的转运测定法,通过自动电热原子吸收分光光度法来确定细胞内的 Si 含量。我们发现,该测定法具有很高的分析灵敏度,Si 的检测下限低于 1µM,也就是说,低于或非常接近动物细胞的浓度范围。我们还发现,该测定法在 Si 转运研究中提供了有效的、具有成本效益的测定结果,同时仅需要可操作数量的样本。因此,这里描述的方案应该成为 Si 转运领域快速发展的黄金标准。

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