Janecki A J, Janecki M, Akhter S, Donowitz M
The University of Texas-Medical School at Houston, Department of Medicine, Division of Gastroenterology, Hepatology, and Nutrition, Houston, Texas 77030, USA.
J Histochem Cytochem. 2000 Nov;48(11):1479-92. doi: 10.1177/002215540004801105.
We developed a confocal morphometric analysis to quantitate the relative plasma membrane (PM) expression of the Na/H exchanger NHE3 in living PS120 fibroblasts. NHE3 is a membrane transport protein that is acutely regulated by changes in the number of molecules expressed at the PM. To quantitate the PM expression of NHE3 under various experimental conditions, we stably expressed a chimera of rabbit NHE3 and green fluorescent protein (NHE3-GFP) in PS120 fibroblasts. A three-dimensional (3D) map of the intracellular distribution of NHE3-GFP was obtained by confocal laser scanning microscopy (CLSM) of cells superfused with a styryl dye, FM 4-64. This fluorophore rapidly and reversibly labeled the outer lipid layer of the PM, which allowed generation of a digital mask of the PM and calculation of the fraction of a total cellular NHE3-GFP expressed at the PM. This analysis was successfully used to quantitate the relative PM expression of NHE3-GFP in control cells (25%) and a decrease in the expression caused by subsequent exposure of cells to wortmannin (5.1%). Reliability of the method was confirmed by cell surface biotinylation, which yielded very similar results. Confocal morphometric analysis is fast and reproducible and could potentially be used for investigations on regulation of expression of other membrane proteins.
我们开发了一种共聚焦形态计量分析方法,用于定量活的PS120成纤维细胞中钠氢交换体NHE3的相对质膜(PM)表达。NHE3是一种膜转运蛋白,其在质膜上表达的分子数量变化可对其进行急性调节。为了在各种实验条件下定量NHE3的质膜表达,我们在PS120成纤维细胞中稳定表达了兔NHE3与绿色荧光蛋白的嵌合体(NHE3-GFP)。通过对用苯乙烯基染料FM 4-64灌注的细胞进行共聚焦激光扫描显微镜(CLSM),获得了NHE3-GFP细胞内分布的三维(3D)图谱。这种荧光团能快速且可逆地标记质膜的外脂质层,从而生成质膜的数字掩码,并计算在质膜上表达的细胞总NHE3-GFP的比例。该分析成功用于定量对照细胞中NHE3-GFP的相对质膜表达(25%),以及细胞随后暴露于渥曼青霉素后导致的表达下降(5.1%)。通过细胞表面生物素化证实了该方法的可靠性,其结果非常相似。共聚焦形态计量分析快速且可重复,可能用于研究其他膜蛋白表达的调控。