Stump R F, Pfeiffer J R, Schneebeck M C, Seagrave J C, Oliver J M
University of New Mexico School of Medicine, Albuquerque 87131.
Am J Anat. 1989 Jun-Jul;185(2-3):128-41. doi: 10.1002/aja.1001850206.
The response of cells to signaling molecules such as hormones, growth factors, and immune mediators that bind to cell-surface receptors depends in part on the density and distribution of the relevant receptors. We have developed methods to map the distribution of IgE receptors on RBL-2H3 mast cells at high resolution in the scanning electron microscope (SEM). The key elements of our procedure are a new fixative that preserves receptor binding activity; a family of colloidal gold-conjugated probes that bind directly or indirectly to the IgE-receptor complex; an SEM with detectors for both secondary and backscattered electrons (to observe surface topography and gold particles, respectively); and an image processor that can average, digitize, and store these images. Topographical maps are generated by processing and superimposing the digitized images. The methods we describe can be applied to study the density and distribution of any membrane receptor that can be labeled with colloidal gold particles.
细胞对诸如激素、生长因子和免疫介质等与细胞表面受体结合的信号分子的反应,部分取决于相关受体的密度和分布。我们已经开发出了一些方法,可在扫描电子显微镜(SEM)下以高分辨率绘制RBL - 2H3肥大细胞上IgE受体的分布图。我们方法的关键要素包括:一种能保留受体结合活性的新型固定剂;一系列直接或间接与IgE受体复合物结合的胶体金偶联探针;一台配备有二次电子和背散射电子探测器(分别用于观察表面形貌和金颗粒)的扫描电子显微镜;以及一台能够对这些图像进行平均、数字化和存储的图像处理器。通过处理和叠加数字化图像生成地形图。我们所描述的方法可用于研究任何能用胶体金颗粒标记的膜受体的密度和分布。