Grote M, Fromme H G
J Histochem Cytochem. 1986 Nov;34(11):1459-64. doi: 10.1177/34.11.3772077.
Ultra-thin sections of vegetative tissues from birch (anthers and leaves) were labeled for pollen antigens and allergens using a commercial rabbit IgG antibody preparation directed against birch pollen antigens and allergens. Antibody binding sites were visualized using the protein A-gold technique. Specific labeling occurred in anther tissue (tape-tum cells, anther wall cells) as well as in the birch leaf (assimilation parenchyma). In both types of tissue, antigens and allergens were detected throughout the living protoplast (including cell organelles such as nuclei, mitochondria, and plastids). The cellulose cell walls were always free from anti-birch-pollen IgG-binding sites. The immunological controls (normal rabbit IgG) showed a low degree of nonspecific labeling. In plant tissues belonging to genera quite different from birch (tulip anther, rhododendron leaves), after incubation with the specific IgG weak labeling was observed. The immunological basis for these results is discussed.
使用针对桦树花粉抗原和过敏原的商业兔IgG抗体制剂,对桦树营养组织(花药和叶片)的超薄切片进行花粉抗原和过敏原标记。采用蛋白A-金技术观察抗体结合位点。在花药组织(绒毡层细胞、花药壁细胞)以及桦树叶(同化薄壁组织)中出现了特异性标记。在这两种组织类型中,在整个活原生质体(包括细胞核、线粒体和质体等细胞器)中都检测到了抗原和过敏原。纤维素细胞壁始终没有抗桦树花粉IgG结合位点。免疫对照(正常兔IgG)显示非特异性标记程度较低。在与桦树差异很大的属的植物组织(郁金香花药、杜鹃花叶片)中,与特异性IgG孵育后观察到微弱标记。讨论了这些结果的免疫学基础。