Alvarez-Leefmans Francisco J, Herrera-Pérez José J, Márquez Martín S, Blanco Víctor M
Department of Pharmacology and Toxicology, Wright State University, Dayton, Ohio 45435, USA.
Biophys J. 2006 Jan 15;90(2):608-18. doi: 10.1529/biophysj.105.069450. Epub 2005 Oct 28.
Regulation and maintenance of cell water volume and intracellular pH (pHi) are vital functions that are interdependent; cell volume regulation affects, and is in turn affected by, changes in pHi. Disruption of either function underlies various pathologies. To study the interaction and kinetics of these two mechanisms, we developed and validated a quantitative fluorescence imaging microscopy method to measure simultaneous changes in pHi and volume in single cells loaded with the fluorescent probe BCECF. CWV is measured at the excitation isosbestic wavelength, whereas pHi is determined ratiometrically. The method has a time resolution of <1 s and sensitivity to osmotic changes of approximately 1%. It can be applied in real time to virtually any cell type attached to a coverslip, independently of cellular shape and geometry. Calibration procedures and algorithms developed to transform fluorescence signals into changes in cell water volume (CWV) and examples of applications are presented.
细胞水体积和细胞内pH值(pHi)的调节与维持是相互依存的重要功能;细胞体积调节会影响pHi的变化,反过来也会受到pHi变化的影响。这两种功能中的任何一种受到破坏都可能导致各种病理状况。为了研究这两种机制的相互作用和动力学,我们开发并验证了一种定量荧光成像显微镜方法,用于测量加载荧光探针BCECF的单个细胞中pHi和体积的同步变化。细胞水体积(CWV)在激发等吸收波长下测量,而pHi则通过比率法测定。该方法的时间分辨率小于1秒,对渗透压变化的敏感度约为1%。它可以实时应用于附着在盖玻片上的几乎任何细胞类型,而不受细胞形状和几何结构的影响。本文介绍了将荧光信号转换为细胞水体积(CWV)变化的校准程序和算法以及应用实例。