Jonchère Vincent, Brionne Aurélien, Gautron Joël, Nys Yves
INRA, UR83 Recherches Avicoles, F-37380, Nouzilly, France.
BMC Physiol. 2012 Sep 4;12:10. doi: 10.1186/1472-6793-12-10.
In Gallus gallus, eggshell formation takes place daily in the hen uterus and requires large amounts of the ionic precursors for calcium carbonate (CaCO3). Both elements (Ca2+, HCO3-) are supplied by the blood via trans-epithelial transport. Our aims were to identify genes coding for ion transporters that are upregulated in the uterine portion of the oviduct during eggshell calcification, compared to other tissues and other physiological states, and incorporate these proteins into a general model for mineral transfer across the tubular gland cells during eggshell formation.
A total of 37 candidate ion transport genes were selected from our database of overexpressed uterine genes associated with eggshell calcification, and by analogy with mammalian transporters. Their uterine expression was compared by qRTPCR in the presence and absence of eggshell formation, and with relative expression levels in magnum (low Ca2+/HCO3- movement) and duodenum (high rates of Ca2+/HCO3- trans-epithelial transfer). We identified overexpression of eleven genes related to calcium movement: the TRPV6 Ca2+ channel (basolateral uptake of Ca2+), 28 kDa calbindin (intracellular Ca2+ buffering), the endoplasmic reticulum type 2 and 3 Ca2+ pumps (ER uptake), and the inositol trisphosphate receptors type 1, 2 and 3 (ER release). Ca2+ movement across the apical membrane likely involves membrane Ca2+ pumps and Ca2+/Na+ exchangers. Our data suggests that Na+ transport involved the SCNN1 channel and the Na+/Ca2+ exchangers SLC8A1, 3 for cell uptake, the Na+/K+ ATPase for cell output. K+ uptake resulted from the Na+/K+ ATPase, and its output from the K+ channels (KCNJ2, 15, 16 and KCNMA1).We propose that the HCO3- is mainly produced from CO2 by the carbonic anhydrase 2 (CA2) and that HCO3- is secreted through the HCO3-/Cl- exchanger SLC26A9. HCO3- synthesis and precipitation with Ca2+ produce two H+. Protons are absorbed via the membrane's Ca2+ pumps ATP2B1, 2 in the apical membrane and the vacuolar (H+)-atpases at the basolateral level. Our model incorporate Cl- ions which are absorbed by the HCO3-/Cl- exchanger SLC26A9 and by Cl- channels (CLCN2, CFTR) and might be extruded by Cl-/H+ exchanger (CLCN5), but also by Na+ K+ 2 Cl- and K+ Cl- cotransporters.
Our Gallus gallus uterine model proposes a large list of ion transfer proteins supplying Ca2+ and HCO3- and maintaining cellular ionic homeostasis. This avian model should contribute towards understanding the mechanisms and regulation for ionic precursors of CaCO3, and provide insight in other species where epithelia transport large amount of calcium or bicarbonate.
在原鸡中,蛋壳形成每天在母鸡子宫内进行,需要大量碳酸钙(CaCO₃)的离子前体。这两种元素(Ca²⁺、HCO₃⁻)通过跨上皮运输由血液供应。我们的目的是鉴定与其他组织和其他生理状态相比,在蛋壳钙化期间输卵管子宫部分上调的离子转运蛋白编码基因,并将这些蛋白质纳入蛋壳形成过程中跨管状腺细胞矿物质转运的通用模型。
从我们与蛋壳钙化相关的子宫过表达基因数据库中,并通过与哺乳动物转运蛋白类比,总共选择了37个候选离子转运基因。通过qRTPCR比较它们在有和没有蛋壳形成时的子宫表达,并与在蛋白分泌部(低Ca²⁺/HCO₃⁻移动)和十二指肠(高Ca²⁺/HCO₃⁻跨上皮转运速率)中的相对表达水平进行比较。我们鉴定出11个与钙转运相关的基因过表达:TRPV6钙通道(Ca²⁺的基底外侧摄取)、28 kDa钙结合蛋白(细胞内Ca²⁺缓冲)、内质网2型和3型钙泵(内质网摄取)以及1型、2型和3型肌醇三磷酸受体(内质网释放)。Ca²⁺跨顶膜的转运可能涉及膜钙泵和Ca²⁺/Na⁺交换器。我们的数据表明,Na⁺转运涉及SCNN1通道和用于细胞摄取的Na⁺/Ca²⁺交换器SLC8A1、3,以及用于细胞输出的Na⁺/K⁺ ATP酶。K⁺摄取由Na⁺/K⁺ ATP酶产生,其输出通过K⁺通道(KCNJ2、15、16和KCNMA1)。我们提出HCO₃⁻主要由碳酸酐酶2(CA2)从CO₂产生,并且HCO₃⁻通过HCO₃⁻/Cl⁻交换器SLC26A9分泌。HCO₃⁻的合成和与Ca²⁺的沉淀产生两个H⁺。质子通过顶膜中的膜钙泵ATP2B1、2和基底外侧水平的液泡(H⁺)-ATP酶吸收。我们的模型纳入了Cl⁻离子,其通过HCO₃⁻/Cl⁻交换器SLC26A9和Cl⁻通道(CLCN2、CFTR)吸收,并且可能通过Cl⁻/H⁺交换器(CLCN5)以及Na⁺ K⁺ 2 Cl⁻和K⁺ Cl⁻共转运体排出。
我们的原鸡子宫模型提出了大量提供Ca²⁺和HCO₃⁻并维持细胞离子稳态的离子转运蛋白。这个禽类模型应该有助于理解CaCO₃离子前体的机制和调节,并为其他上皮细胞运输大量钙或碳酸氢盐的物种提供见解。