Cimini V, Van Noorden S, Mahadeva H, Polak J M
Department of Human Anatomy, Medical School, Federico II University of Naples, Italy.
Histochem J. 1994 Jan;26(1):59-66.
We have investigated the efficacy of the cell blot assay in analysis of the secretion of hormones and peptides from rat anterior pituitary cells. The dissociated cells are cultured on pieces of translucent polyvinylidene difluoride membrane, on which their secretory products are adsorbed and subsequently immunostained. The area and integrated optical density of the stained 'halo' surrounding individual cells is measured by microscopical image processing and the values for basal secretion of a particular hormone or peptide are compared with those after application of secretagogues or inhibitors. Our experiments tested established responses of dissociated rat anterior pituitary cells; in general, the results were as expected. Double immunoenzymatic staining could be used to show secretion of two products from the same or different cells in one preparation, and immunofluorescence with fluorescein- and/or rhodamine-labelled antibodies could be used instead of enzyme-linked immunolabelling. Optimal dilutions of immunoreagents were much higher than those used for immunocytochemistry on tissue sections. Although the cell blot assay does not provide absolute quantification, since some of the secreted product escapes into the medium, it is a relatively easy and economical way for morphologists to compare secretion from individual cells under varying conditions.
我们研究了细胞印迹分析在大鼠垂体前叶细胞激素和肽分泌分析中的功效。将解离的细胞培养在半透明聚偏二氟乙烯膜片上,其分泌产物吸附在膜片上,随后进行免疫染色。通过显微镜图像处理测量单个细胞周围染色“晕圈”的面积和积分光密度,并将特定激素或肽的基础分泌值与应用促分泌剂或抑制剂后的数值进行比较。我们的实验检测了大鼠垂体前叶解离细胞的既定反应;总体而言,结果符合预期。双免疫酶染色可用于在一份标本中显示同一细胞或不同细胞分泌的两种产物,并且可用荧光素和/或罗丹明标记抗体进行免疫荧光检测,以替代酶联免疫标记。免疫试剂的最佳稀释度远高于用于组织切片免疫细胞化学的稀释度。尽管细胞印迹分析不能提供绝对定量,因为一些分泌产物会逸入培养基中,但对于形态学家来说,它是一种相对简单且经济的方法,可用于比较不同条件下单个细胞的分泌情况。