在爪蟾卵母细胞中表达的斑马鱼 Slc12a10.1 的电中性 Na+/Cl- 共转运活性。

IF 2.2 3区 医学 Q3 PHYSIOLOGY American journal of physiology. Regulatory, integrative and comparative physiology Pub Date : 2024-08-01 Epub Date: 2024-06-06 DOI:10.1152/ajpregu.00096.2024
Chihiro Ota, Ayumi Nagashima, Akira Kato
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引用次数: 0

摘要

Na+/Cl- 共转运体 2(Ncc2 或 Slc12a10)是一种膜转运蛋白,属于电中性阳离子-氯化物共转运体家族。Slc12a10 基因(slc12a10)广泛存在于有骨脊椎动物中,但在鸟类、某些有骨鱼类和大多数哺乳动物中被删除或假基因化。Slc12a10与Ncc(Slc12a3或Ncc1)高度同源;然而,只有少数报道测量了Slc12a10的活性。在本研究中,我们重点研究了斑马鱼 Slc12a10.1(zSlc12a10.1),并利用爪蟾卵母细胞电生理学分析了其活性。使用 Na+ 选择性微电极进行的分析表明,zSlc12a10.1 卵母细胞的细胞内钠活性(aNai)在无 Na+ 或无 Cl- 的培养基中显著降低,而当培养基中重新加入 Na+ 或 Cl- 时则恢复。使用 Cl--选择性微电极进行的类似分析表明,zSlc12a10.1 卵母细胞的胞内氯离子活性(aCli)在无 Na+ 或 Cl--的培养基中明显降低,而当在培养基中加入 Na+ 或 Cl--时又会恢复。用电压钳进行类似实验时,当zSlc12a10.1卵母细胞的aNai在无Na+培养基中降低时,膜电流没有变化。分子系统发育和同源关系分析表明,斑马鱼中 slc12a10.2 和 slc12a10.3 之间的基因重复是一个相对较新的事件,而 slc12a10.1 和 slc12a10.2/slc12a10.3 的祖先基因之间的基因重复是一个相对较新的事件。在斑马鱼 Ictaluridae、Salmoniformes、Osmeriformes、Batrachoididae、Syngnathiformes、Gobiesociformes、Labriformes 和 Tetraodontiformes 的物种中观察到了 slc12a10 缺乏。这些结果表明斑马鱼 Slc12a10.1 是一种电中性 Na+/Cl 共转运体,并确立了它在各种远洋鱼类 slc12a10 旁系亲属中的进化地位。
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Electroneutral Na+/Cl- cotransport activity of zebrafish Slc12a10.1 expressed in Xenopus oocytes.

Na+/Cl- cotransporter 2 (Ncc2 or Slc12a10) is a membrane transport protein that belongs to the electroneutral cation-chloride cotransporter family. The Slc12a10 gene (slc12a10) is widely present in bony vertebrates but is deleted or pseudogenized in birds, some bony fishes, and most mammals. Slc12a10 is highly homologous to Ncc (Slc12a3 or Ncc1); however, there are only a few reports measuring the activity of Slc12a10. In this study, we focused on zebrafish Slc12a10.1 (zSlc12a10.1) and analyzed its activity using Xenopus oocyte electrophysiology. Analysis using Na+-selective microelectrodes showed that intracellular sodium activity (aNai) in zSlc12a10.1 oocytes was significantly decreased in Na+- or Cl--free medium and recovered when Na+ or Cl- was readded to the medium. Similar analysis using a Cl--selective microelectrode showed that intracellular chloride activity (aCli) in zSlc12a10.1 oocytes significantly decreased in Na+- or Cl--free medium and recovered when Na+ or Cl- was readded to the medium. When a similar experiment was performed with a voltage clamp, the membrane current did not change when aNai of zSlc12a10.1 oocytes was decreased in Na+-free medium. Molecular phylogenetic and synteny analyses suggest that gene duplication between slc12a10.2 and slc12a10.3 in zebrafish is a relatively recent event, whereas gene duplication between slc12a10.1 and the ancestral gene of slc12a10.2/slc12a10.3 occurred at least about 2 million years ago. slc12a10 deficiency was observed in species belonging to Ictaluridae, Salmoniformes, Osmeriformes, Batrachoididae, Syngnathiformes, Gobiesociformes, Labriformes, and Tetraodontiformes. These results indicate that zebrafish Slc12a10.1 is an electroneutral Na+/Cl-cotransporter and establish its evolutionary position among various teleost slc12a10 paralogs.NEW & NOTEWORTHY Na+/Cl- cotransporter 2 (Slc12a10; Ncc2) is a protein highly homologous to Ncc (Slc12a3; Ncc1); however, there are only a few reports measuring the activity of Slc12a10. Electrophysiological analysis of Xenopus oocytes expressing zebrafish Slc12a10.1 showed that Slc12a10.1 acts as an electroneutral Na+/Cl-cotransporter. This is the third report on the activity of Slc12a10, following previous reports on Slc12a10 in eels.

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来源期刊
CiteScore
5.30
自引率
3.60%
发文量
145
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Regulatory, Integrative and Comparative Physiology publishes original investigations that illuminate normal or abnormal regulation and integration of physiological mechanisms at all levels of biological organization, ranging from molecules to humans, including clinical investigations. Major areas of emphasis include regulation in genetically modified animals; model organisms; development and tissue plasticity; neurohumoral control of circulation and hypertension; local control of circulation; cardiac and renal integration; thirst and volume, electrolyte homeostasis; glucose homeostasis and energy balance; appetite and obesity; inflammation and cytokines; integrative physiology of pregnancy-parturition-lactation; and thermoregulation and adaptations to exercise and environmental stress.
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