Gregório Sílvia F, Carvalho Edison S M, Campinho Marco A, Power Deborah M, Canário Adelino V M, Fuentes Juan
Centre of Marine Sciences (CCMar), Campus de Gambelas, Universidade do Algarve, 8005-139 Faro, Portugal.
J Exp Biol. 2014 May 1;217(Pt 9):1555-62. doi: 10.1242/jeb.098517. Epub 2014 Feb 5.
In marine fish, high epithelial bicarbonate secretion by the intestine generates luminal carbonate precipitates of divalent cations that play a key role in water and ion homeostasis. In vitro studies highlight the involvement of the calciotropic hormones PTHrP (parathyroid hormone-related protein) and stanniocalcin (STC) in the regulation of epithelial bicarbonate transport. The present study tested the hypothesis that calciotropic hormones have a regulatory role in carbonate precipitate formation in vivo. Sea bream (Sparus aurata) juveniles received single intraperitoneal injections of piscine PTHrP(1-34), the PTH/PTHrP receptor antagonist PTHrP(7-34) or purified sea bream STC, or were passively immunized with polyclonal rabbit antisera raised against sea bream STC (STC-Ab). Endocrine effects on the expression of the basolateral sodium bicarbonate co-transporter (Slc4a4.A), the apical anion exchangers Slc26a6.A and Slc26a3.B, and the V-type proton pump β-subunit (Atp6v1b) in the anterior intestine were evaluated. In keeping with their calciotropic nature, the hypocalcaemic factors PTHrP(7-34) and STC up-regulated gene expression of all transporters. In contrast, the hypercalcaemic factor PTHrP(1-34) and STC antibodies down-regulated transporters involved in the bicarbonate secretion cascade. Changes in intestine luminal precipitate contents provoked by calcaemic endocrine factors validated these results: 24 h post-injection either PTHrP(1-34) or immunization with STC-Ab reduced the carbonate precipitate content in the sea bream intestine. In contrast, the PTH/PTHrP receptor antagonist PTHrP(7-34) increased not only the precipitated fraction but also the concentration of HCO3(-) equivalents in the intestinal fluid. These results confirm the hypothesis that calciotropic hormones have a regulatory role in carbonate precipitate formation in vivo in the intestine of marine fish. Furthermore, they illustrate for the first time in fish the counteracting effect of PTHrP and STC, and reveal an unexpected contribution of calcaemic factors to acid-base balance.
在海水鱼中,肠道上皮细胞大量分泌碳酸氢盐会产生管腔中二价阳离子的碳酸盐沉淀,这在水和离子稳态中起关键作用。体外研究强调了促钙激素甲状旁腺激素相关蛋白(PTHrP)和鲽鱼降钙素(STC)参与上皮细胞碳酸氢盐转运的调节。本研究检验了促钙激素在体内碳酸盐沉淀形成中具有调节作用这一假设。对鲷鱼幼鱼进行单次腹腔注射鱼PTHrP(1 - 34)、PTH/PTHrP受体拮抗剂PTHrP(7 - 34)或纯化的鲷鱼STC,或者用针对鲷鱼STC产生的多克隆兔抗血清(STC - Ab)进行被动免疫。评估了内分泌对前肠基底外侧钠碳酸氢盐共转运体(Slc4a4.A)、顶端阴离子交换体Slc26a6.A和Slc26a3.B以及V型质子泵β亚基(Atp6v1b)表达的影响。与它们的促钙特性一致,低血钙因子PTHrP(7 - 34)和STC上调了所有转运体的基因表达。相反,高血钙因子PTHrP(1 - 34)和STC抗体下调了参与碳酸氢盐分泌级联反应的转运体。由血钙内分泌因子引起的肠管腔沉淀含量变化证实了这些结果:注射PTHrP(1 - 34)或用STC - Ab免疫后24小时,降低了鲷鱼肠道中的碳酸盐沉淀含量。相反,PTH/PTHrP受体拮抗剂PTHrP(7 - 34)不仅增加了沉淀部分,还增加了肠液中HCO3(-)当量的浓度。这些结果证实了促钙激素在海水鱼肠道体内碳酸盐沉淀形成中具有调节作用这一假设。此外,它们首次在鱼类中阐明了PTHrP和STC的拮抗作用,并揭示了血钙因子对酸碱平衡的意外贡献。