首页> 外文期刊>Microscopy research and technique >Morphological and ultrastructural characterization of ionoregulatory cells in the teleost oreochromis niloticus following salinity challenge combining complementary confocal scanning laser microscopy and transmission electron microscopy using a novel prefixation immunogold labeling technique
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Morphological and ultrastructural characterization of ionoregulatory cells in the teleost oreochromis niloticus following salinity challenge combining complementary confocal scanning laser microscopy and transmission electron microscopy using a novel prefixation immunogold labeling technique

机译:盐度挑战后,硬骨鱼嗜盐菌电离调节细胞的形态学和超微结构特征结合了互补共聚焦扫描激光显微镜和透射电子显微镜,采用了一种新型的前缀免疫金标记技术

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摘要

Aspects of ionoregulatory or mitochondria-rich cell (MRC) differentiation and adaptation in Nile tilapia yolk-sac larvae following transfer from freshwater to elevated salinities, that is, 12.5 and 20 ppt are described. Investigations using immunohistochemistry on whole-mount Nile tilapia larvae using anti- Na~+/K~+-ATPase as a primary antibody and Fluoronanogold~(?) (Nanoprobes) as a secondary immunoprobe allowed fluorescent labeling with the high resolution of confocal scanning laser microscopy combined with the detection of immunolabeled target molecules at an ultrastructural level using transmission electron microscopy (TEM). It reports, for the first time, various developmental stages of MRCs within the epithelial layer of the tail of yolk-sac larvae, corresponding to immature, developing, and mature MRCs, identifiable by their own characteristic ultrastructure and form. Following transfer to hyperosmotic salinities the density of immunogold particles and well as the intricacy of the tubular system appeared to increase. In addition, complementary confocal scanning laser microscopy allowed identification of immunopositive ramifying extensions that appeared to emanate from the basolateral portion of the cell that appeared to be correlated with the localization of subsurface tubular areas displaying immunogold labeled Na~+/K~+-ATPase. This integrated approach describes a reliable and repeatable prefixation immunogold labeling technique allowing precise visualization of NaK within target cells combined with a 3D imaging that offers valuable insights into MRC dynamics at an ultrastructural level. Microsc. Res. Tech., 76:1016-1024, 2013.
机译:从淡水转移到高盐度(即12.5和20 ppt)后,描述了尼罗罗非鱼卵黄囊幼虫中离子调节或线粒体富集细胞(MRC)的分化和适应方面。以抗Na〜+ / K〜+ -ATPase为一抗,以Fluoronanogold〜(?)(Nanoprobes)为第二免疫探针,通过免疫组化技术对整个尼罗罗非鱼幼虫进行免疫研究,从而可以使用高分辨率的共聚焦扫描激光进行荧光标记显微镜结合使用透射电子显微镜(TEM)在超微结构水平上检测免疫标记的靶分子。它首次报道了卵黄囊幼虫尾巴上皮层中的MRCs的不同发​​育阶段,对应于未成熟,发育和成熟的MRCs,可通过其自身的特征性超微结构和形式对其进行鉴定。转移到高渗盐度后,免疫金颗粒的密度和肾小管系统的复杂性似乎增加了。另外,互补共聚焦扫描激光显微镜可以鉴定似乎从细胞的基底外侧部分发散的免疫阳性分支延伸,这些延伸似乎与显示免疫金标记的Na〜+ / K〜+ -ATPase的地下肾小管区域的定位有关。这种集成方法描述了一种可靠且可重复的前缀免疫金标记技术,该技术可将靶细胞内的NaK精确可视化,并与3D成像相结合,从而可提供有关超微结构水平MRC动力学的宝贵见解。 Microsc。 Res。 Tech。,76:1016-1024,2013。

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