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首页> 外文期刊>Fish Physiology and Biochemistry >Structural differentiation of apical openings in active mitochondria-rich cells during early life stages of Nile tilapia (Oreochromis niloticus L.) as a response to osmotic challenge
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Structural differentiation of apical openings in active mitochondria-rich cells during early life stages of Nile tilapia (Oreochromis niloticus L.) as a response to osmotic challenge

机译:尼罗罗非鱼(Oreochromis niloticus L.)生命早期阶段对活动线粒体富集细胞顶端开口的结构分化,以应对渗透挑战

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This study examines the structural differentiation of the apical crypts of mitochondria-rich cells (MRCs) in Nile tilapia as a response to osmotic challenge. Larvae were transferred from freshwater at 3 days post-hatch to 12.5 and 20 ppt and were sampled at 24- and 48-h post-transfer. Scanning electron microscopy allowed quantification of MRCs, based on apical crypt appearance and surface area, resulting in a morphological classification of 'sub-types', that is, Type I or absorptive (surface area range 5.2-19.6 mu m(2)), Type II or active absorptive form (surface area range 1.1-15.7 mu m(2)), Type III or weakly functioning form (surface area range 0.08-4.6 mu m(2)) and Type IV or active secreting form (surface area range 4.1-11.7 mu m(2)). Mucus cell crypts were discriminated from those of MRCs based on the presence of globular extensions and quantified. Density and frequency of MRCs and mucus cells varied significantly according to the experimental salinity and time post-transfer; in freshwater-adapted larvae, all types were present except Type IV but, following transfer to elevated salinities, Type I and Type II disappeared and appeared to be replaced by Type IV crypts. Type III crypt density remained constant following transfer. Transmission electron microscopy with immunogold labelling, using a novel pre-fixation technique with anti-Na+/K+-ATPase, allowed complementary ultrastructural visualisation of specific localisation of the antibodies on active MRCs, permitting a review of MRC apical morphology and related Na+/K+-ATPase binding sites.
机译:这项研究检查了尼罗罗非鱼中富含线粒体细胞(MRC)顶隐窝的结构分化,以应对渗透挑战。孵化后3天将幼虫从淡水中转移到12.5和20 ppt,并在转移后24和48小时取样。扫描电子显微镜允许根据根隐窝的外观和表面积对MRC进行定量,从而形成“亚型”的形态分类,即I型或吸收型(表面积范围5.2-19.6μm(2)), II型或活性吸收形式(表面积范围1.1-15.7μm(2)),III型或功能弱的形式(表面积范围0.08-4.6μm(2))和IV型或活性分泌形式(表面积范围) 4.1-11.7微米(2))。基于球状延伸的存在,将粘液细胞隐窝与MRC区分开,并进行定量。 MRC和粘液细胞的密度和频率根据实验盐度和转移后的时间而有显着变化。在适应淡水的幼虫中,除IV型外均存在所有类型的幼虫,但在转移到较高的盐度后,I型和II型消失了,似乎被IV型隐窝所取代。转移后,III型隐窝密度保持恒定。使用带有抗Na + / K + -ATPase的新型预固定技术,采用带有免疫金标记的透射电子显微镜,可以对超微结构的可视化抗体在活性MRC上的特异性定位进行互补可视化,从而可以回顾MRC的根尖形态和相关的Na + / K +- ATPase结合位点。

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