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采用新型预固定免疫胶体金标记技术,结合共聚焦扫描激光显微镜和透射电子显微镜,对盐度胁迫下罗非鱼 Oreochromis niloticus 中离子调节细胞的形态和超微结构进行了特征描述。

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.

机构信息

Institute of Aquaculture, University of Stirling, FK9 3LA, Scotland; Fish Health Laboratory, French Associates' Institute for Agriculture and Biotechnology of Drylands, Blaustein Institute for Desert Research, Ben Gurion University, Sede-Boqer Campus, 84990, Israel.

出版信息

Microsc Res Tech. 2013 Oct;76(10):1016-24. doi: 10.1002/jemt.22262. Epub 2013 Jul 19.

Abstract

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.

摘要

描述了尼罗罗非鱼卵黄囊幼虫从淡水转移到高盐度(即 12.5 和 20 ppt)后,离子调节或富含线粒体的细胞(MRC)分化和适应的各个方面。使用抗 Na⁺/K⁺-ATPase 作为一抗,Fluoronanogold™(Nanoprobes)作为二抗,对整个尼罗罗非鱼幼虫进行免疫组织化学染色,结合共聚焦扫描激光显微镜的高分辨率和透射电子显微镜(TEM)的超微结构水平检测免疫标记的靶分子,首次报道了卵黄囊幼虫尾部上皮层内 MRC 的各种发育阶段,包括未成熟、发育中和成熟的 MRC,可通过其自身的特征超微结构和形态来识别。转移到高渗盐度后,免疫金颗粒的密度以及管状系统的复杂性似乎增加了。此外,互补的共聚焦扫描激光显微镜允许鉴定出免疫阳性的分支延伸,这些分支似乎从细胞的基底外侧部分发出,这似乎与显示免疫金标记 Na⁺/K⁺-ATPase 的亚表面管状区域的定位相关。这种综合方法描述了一种可靠且可重复的预固定免疫金标记技术,允许精确观察靶细胞内的 NaK,并结合 3D 成像,为 MRC 在超微结构水平的动态提供有价值的见解。

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