Sugiura Shozo H, McDaniel Nichole K, Ferraris Ronaldo P
Department of Pharmacology and Physiology, New Jersey Medical School, Newark, NJ 07103, USA.
Am J Physiol Regul Integr Comp Physiol. 2003 Oct;285(4):R770-81. doi: 10.1152/ajpregu.00127.2003. Epub 2003 Jun 19.
Mammalian type II sodium-phosphate cotransporter (NaPi-II) and inorganic phosphate uptake stimulator (PiUS) genes are upregulated by dietary phosphorus (P) restriction to increase intestinal and renal P transport, but little is known about NaPi-II and PiUS regulation in other vertebrates. We studied the 1). the tissue distribution and dietary regulation of NaPi-II, PiUS, and sodium-glucose cotransporter (SGLT1) mRNA and NaPi-II protein in juvenile rainbow trout (Oncorhynchus mykiss) and 2). effects of dietary P on intestinal Pi absorption in vivo. NaPi-II, PiUS, and SGLT1 mRNA were found in the proximal and distal intestine, pyloric ceca, and kidney. PiUS mRNA was also found in the heart, gill, blood, stomach, liver, skin, and muscle. Tissue distribution of NaPi-II protein correlated with that of NaPi-II mRNA except in gill ionocytes where NaPi-II antibodies recognized related epitopes. Chronic consumption of a low-P diet increased NaPi-II and PiUS but not SGLT1 mRNA abundance in the intestine and kidney. Unlike mammals, there was no detectable shift in tissue or cellular localization of NaPi-II protein in response to dietary P restriction. Regulation of NaPi and PiUS mRNA expression was observed only in fish grown under optimal aqueous oxygen concentrations. In vivo fractional absorption of Pi by the intestine decreased in fish fed high-P diets. Decreases in absorption were less pronounced in fish previously fed low-P diets, suggesting that diet history modulates acute regulation of P absorption. Regulation of dietary Pi absorption in vivo may involve a specific change in intestinal NaPi-II and PiUS gene expression.
哺乳动物II型钠-磷酸盐共转运体(NaPi-II)和无机磷酸盐摄取刺激因子(PiUS)基因会因饮食中磷(P)的限制而上调,以增加肠道和肾脏对磷的转运,但对于其他脊椎动物中NaPi-II和PiUS的调节情况却知之甚少。我们研究了1). 幼年虹鳟(Oncorhynchus mykiss)中NaPi-II、PiUS和钠-葡萄糖共转运体(SGLT1)mRNA以及NaPi-II蛋白的组织分布和饮食调节,以及2). 饮食中的磷对体内肠道磷吸收的影响。在近端和远端肠道、幽门盲囊和肾脏中发现了NaPi-II、PiUS和SGLT1 mRNA。在心脏、鳃、血液、胃、肝脏、皮肤和肌肉中也发现了PiUS mRNA。NaPi-II蛋白的组织分布与NaPi-II mRNA的分布相关,但在鳃离子细胞中除外,在那里NaPi-II抗体识别相关表位。长期食用低磷饮食会增加肠道和肾脏中NaPi-II和PiUS的含量,但不会增加SGLT1 mRNA的丰度。与哺乳动物不同,饮食中磷的限制并未导致NaPi-II蛋白在组织或细胞定位上发生可检测到的变化。仅在最佳水体氧浓度下生长的鱼类中观察到了NaPi和PiUS mRNA表达的调节。喂食高磷饮食的鱼类中,肠道对磷的体内分数吸收降低。先前喂食低磷饮食的鱼类中吸收的降低不太明显,这表明饮食史会调节磷吸收的急性调节。体内饮食中磷吸收的调节可能涉及肠道NaPi-II和PiUS基因表达的特定变化。