Roch A M, Nicolas M T, Quash G
Laboratoire d'Immunochimie, Faculté de Médecine Lyon-Sud, Oullins, France.
Histochem Cell Biol. 1997 Apr;107(4):303-12. doi: 10.1007/s004180050115.
Polyamines have been localized at the ultrastructural level in HeLa cells subjected first to fast-freezing fixation (FFF)-freeze substitution (FS) and then to an immunocytochemical method combining anti-polyamine antibodies and immunogold labelling. Polyamines were found in both the cytoplasm and the nucleus and, in the latter, particularly over the dense chromatin area. To our knowledge, this is the first example of the electron microscopic localization of a hapten after FFF-FS. For the preservation of fine ultrastructural details, this FFF-FS method is not only adequate but also greatly reduces, if not totally eliminates, any leeching-out and redistribution of the polyamines during the preparation of the sample. For the preservation of antigenicity in situ during FS, epoxy resin was more effective than hydrophilic LR white resin, probably due to the solubility of polyamines in the latter.
多胺已在超微结构水平上定位到首先经过快速冷冻固定(FFF)-冷冻置换(FS)、然后采用结合抗多胺抗体和免疫金标记的免疫细胞化学方法处理的HeLa细胞中。在细胞质和细胞核中均发现了多胺,在细胞核中,尤其在致密染色质区域。据我们所知,这是FFF-FS后半抗原的电子显微镜定位的首个实例。为了保存精细的超微结构细节,这种FFF-FS方法不仅足够,而且即使不能完全消除,也能大大减少样品制备过程中多胺的任何渗出和重新分布。为了在FS过程中原位保存抗原性,环氧树脂比亲水性LR白色树脂更有效,这可能是由于多胺在后者中的溶解性。