Morales S, Jiménez-López J C, Castro A J, Rodríguez-García M I, Alché J D
Department of Biochemistry, Cell and Molecular Biology of Plants, Estación Experimental del Zaidin. CSIC, Profesor Albareda, 1, 18008 Granada, Spain.
J Microsc. 2008 Aug;231(2):332-41. doi: 10.1111/j.1365-2818.2008.02044.x.
Pollen allergens offer a dual perspective of study: some of them are considered key proteins for pollen physiology, but they are also able to trigger allergy symptoms in susceptible humans after coming in contact with their tissues. Profilin (Ole e 2 allergen) has been characterized, to some extent, as one of the major allergens from Olea europaea L. pollen, a highly allergenic species in the Mediterranean countries. In order to obtain clues regarding the biological role of this protein, we have analyzed both its cellular localization and the organization of actin throughout pollen hydration and early pollen tube germination. The localization of the cited proteins was visualized by confocal laser scanning microscopy immunofluorescence using different antibodies. Upon pollen hydration and pollen germination, a massive presence of profilin was detected close to the site of pollen tube emergence, forming a ring-like structure around the 'effective' apertural region. Profilin was also detected in the pollen exine of the germinating pollen grains and in the germination medium. After using a permeabilization-enhanced protocol for immunolocalization, profilin was also localized in the cytoplasm of the pollen tube, particularly at both the proximal and apical ends. Noticeable accumulations of actin were observed in the cytoplasm of the pollen tube; particularly, in both the apical region and the area immediately close to the aperture. Actin filaments were not observed, probably due to the need of further enhanced fixation procedures. The ultrastructural localization of profilin showed the presence of the protein in the cytoplasm of both the mature pollen grain and the pollen tube. The results shown here could be interpreted as signs of a massive dissociation of the actin-profilin complexes, mobilization of actin monomers, and therefore, an intense activity of the actin cytoskeleton. The extensive release of allergenic proteins from the pollen grain into the surrounding aqueous media, as described here for profilin, may help us to understand the mechanisms by which these allergens might come in contact with the human mucosa, therefore triggering the symptoms of allergy.
其中一些被认为是花粉生理学的关键蛋白质,但它们在接触易感人群的组织后也能够引发过敏症状。肌动蛋白结合蛋白(油橄榄2号过敏原)在一定程度上已被鉴定为油橄榄花粉的主要过敏原之一,油橄榄是地中海国家中一种高度致敏的物种。为了获取有关该蛋白质生物学作用的线索,我们分析了其细胞定位以及在花粉水合和花粉管早期萌发过程中肌动蛋白的组织情况。使用不同抗体通过共聚焦激光扫描显微镜免疫荧光观察上述蛋白质的定位。在花粉水合和花粉萌发时,在花粉管出现部位附近检测到大量肌动蛋白结合蛋白,在“有效”萌发孔区域周围形成环状结构。在萌发花粉粒的花粉外壁和萌发培养基中也检测到了肌动蛋白结合蛋白。在使用增强通透性的免疫定位方案后,肌动蛋白结合蛋白也定位在花粉管的细胞质中,特别是在近端和顶端。在花粉管的细胞质中观察到明显的肌动蛋白积累;特别是在顶端区域和紧邻萌发孔的区域。未观察到肌动蛋白丝,可能是由于需要进一步增强固定程序。肌动蛋白结合蛋白的超微结构定位显示该蛋白质存在于成熟花粉粒和花粉管的细胞质中。此处所示结果可解释为肌动蛋白 - 肌动蛋白结合蛋白复合物大量解离、肌动蛋白单体动员的迹象,因此也是肌动蛋白细胞骨架强烈活动的迹象。如本文所述,致敏蛋白从花粉粒大量释放到周围水性介质中,可能有助于我们理解这些过敏原与人体黏膜接触从而引发过敏症状的机制。