Visualization in zebrafish larvae of Na+ uptake in mitochondria-rich cells whose differentiation is dependent on foxi3a

被引:119
作者
Esaki, Masahiro
Hoshijima, Kazuyuki
Kobayashi, Sayako
Fukuda, Hidekazu
Kawakami, Koichi
Hirose, Shigehisa
机构
[1] Tokyo Inst Technol, Dept Biol Sci, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[2] Natl Inst Genet, Div Mol & Dev Biol, Mishima, Shizuoka 411, Japan
关键词
chloride cell; Sodium Green; Na+/H+ exchanger; vacuolar-type H+-ATPase;
D O I
10.1152/ajpregu.00200.2006
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Uptake of Na+ from the environment is an indispensable strategy for the survival of freshwater fish, as they easily lose Na+ from the plasma to a diluted environment. Nevertheless, the location of and molecules involved in Na+ uptake remain poorly understood. In this study, we utilized Sodium Green, a Na+-dependent fluorescent reagent, to provide direct evidence that Na+ absorption takes place in a subset of the mitochondria-rich (MR) cells on the yolk sac surface of zebrafish larvae. Combined with immunohistochemistry, we revealed that the Na+-absorbing MR cells were exceptionally rich in vacuolar-type H+-ATPase (H+-ATPase) but moderately rich in Na+-K+-ATPase. We also addressed the function of foxi3a, a transcription factor that is specifically expressed in the H+-ATPase-rich MR cells. When foxi3a was depleted from zebrafish embryos by antisense morpholino oligonucleotide injection, differentiation of the MR cells was completely blocked and Na+ influx was severely reduced, indicating that MR cells are the primary sites for Na+ absorption. Additionally, foxi3a expression is initiated at the gastrula stage in the presumptive ectoderm; thus, we propose that foxi3a is a key gene in the control of MR cell differentiation. We also utilized a set of ion transport inhibitors to assess the molecules involved in the process and discuss the observations.
引用
收藏
页码:R470 / R480
页数:11
相关论文
共 64 条
[1]  
*AM PHYS SOC, 2002, AM J PHYSIOL-REG I, V283, pR281, DOI DOI 10.1152/AJPREGU.00279.2002
[2]   INTRACELLULAR NA+ MEASUREMENTS USING SODIUM GREEN TETRAACETATE WITH FLOW-CYTOMETRY [J].
AMORINO, GP ;
FOX, MH .
CYTOMETRY, 1995, 21 (03) :248-256
[3]  
AVELLA M, 1989, J EXP BIOL, V142, P155
[4]   Sodium and chloride transport in zebrafish soft water and hard water acclimated (Danio rerio) [J].
Boisen, AMZ ;
Amstrup, J ;
Novak, I ;
Grosell, M .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1618 (02) :207-218
[5]   BAFILOMYCINS - A CLASS OF INHIBITORS OF MEMBRANE ATPASES FROM MICROORGANISMS, ANIMAL-CELLS, AND PLANT-CELLS [J].
BOWMAN, EJ ;
SIEBERS, A ;
ALTENDORF, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (21) :7972-7976
[6]   Cl- uptake mechanism in freshwater-adapted tilapia (Oreochromis mossambicus) [J].
Chang, IC ;
Hwang, PP .
PHYSIOLOGICAL AND BIOCHEMICAL ZOOLOGY, 2004, 77 (03) :406-414
[7]   A putative H+-K+-ATPase in the Atlantic stingray, Dasyatis sabina:: primary sequence and expression in gills [J].
Choe, KP ;
Verlander, JW ;
Wingo, CS ;
Evans, DH .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2004, 287 (04) :R981-R991
[8]   NHE3 in an ancestral vertebrate: primary sequence, distribution, localization, and function in gills [J].
Choe, KP ;
Kato, A ;
Hirose, S ;
Plata, C ;
Sindic, A ;
Romero, MF ;
Claiborne, JB ;
Evans, DH .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2005, 289 (05) :R1520-R1534
[9]   Acid-base regulation in fishes: Cellular and molecular mechanisms [J].
Claiborne, JB ;
Edwards, SL ;
Morrison-Shetlar, AI .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 2002, 293 (03) :302-319
[10]   Sodium, net acid and ammonia fluxes in freshwater-adapted European flounder (Platichthys flesus L.).: Pharmacological inhibition and effects on gill ventilation volume [J].
Clarke, AP ;
Potts, WTW .
JOURNAL OF ZOOLOGY, 1998, 246 :427-432