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

被引:5
|
作者
Fridman, S. [1 ,2 ]
Rana, K. J. [1 ,3 ]
Bron, J. E. [1 ]
机构
[1] Univ Stirling, Inst Aquaculture, Stirling FK9 3LA, Scotland
[2] Ben Gurion Univ Negev, Blaustein Inst Desert Res, French Associates Inst Agr & Biotechnol Drylands, IL-84990 Beer Sheva, Israel
[3] Univ Stellenbosch, Aquaculture Div, ZA-7602 Stellenbosch, South Africa
关键词
Mitochondria-rich cells; Osmoregulation; Cellular differentiation; Nile tilapia; Ontogeny; CHLORIDE CELLS; FRESH-WATER; MOZAMBIQUE TILAPIA; FUNCTIONAL CLASSIFICATION; MOSSAMBICUS EMBRYOS; GILL ARCH; FISH GILL; MORPHOLOGY; TELEOST; SALINITY;
D O I
10.1007/s10695-012-9767-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1101 / 1114
页数:14
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