Physiology & Biomedical Engineering, Mayo Clinic College of Medicine & Science, 200 1st Street SW, Rochester, MN 55905, USA.
Biochemistry & Molecular Biology, Mayo Clinic College of Medicine & Science, 200 1st Street SW, Rochester, MN, USA.
Pflugers Arch. 2024 Apr;476(4):479-503. doi: 10.1007/s00424-024-02937-w. Epub 2024 Mar 27.
Cellular and organism survival depends upon the regulation of pH, which is regulated by highly specialized cell membrane transporters, the solute carriers (SLC) (For a comprehensive list of the solute carrier family members, see: https://www.bioparadigms.org/slc/ ). The SLC4 family of bicarbonate (HCO) transporters consists of ten members, sorted by their coupling to either sodium (NBCe1, NBCe2, NBCn1, NBCn2, NDCBE), chloride (AE1, AE2, AE3), or borate (BTR1). The ionic coupling of SLC4A9 (AE4) remains controversial. These SLC4 bicarbonate transporters may be controlled by cellular ionic gradients, cellular membrane voltage, and signaling molecules to maintain critical cellular and systemic pH (acid-base) balance. There are profound consequences when blood pH deviates even a small amount outside the normal range (7.35-7.45). Chiefly, Na-coupled bicarbonate transporters (NCBT) control intracellular pH in nearly every living cell, maintaining the biological pH required for life. Additionally, NCBTs have important roles to regulate cell volume and maintain salt balance as well as absorption and secretion of acid-base equivalents. Due to their varied tissue expression, NCBTs have roles in pathophysiology, which become apparent in physiologic responses when their expression is reduced or genetically deleted. Variations in physiological pH are seen in a wide variety of conditions, from canonically acid-base related conditions to pathologies not necessarily associated with acid-base dysfunction such as cancer, glaucoma, or various neurological diseases. The membranous location of the SLC4 transporters as well as recent advances in discovering their structural biology makes them accessible and attractive as a druggable target in a disease context. The role of sodium-coupled bicarbonate transporters in such a large array of conditions illustrates the potential of treating a wide range of disease states by modifying function of these transporters, whether that be through inhibition or enhancement.
细胞和生物的存活依赖于 pH 值的调节,而 pH 值的调节又依赖于高度专业化的细胞膜转运蛋白,即溶质载体(SLC)(有关溶质载体家族成员的综合列表,请参见:https://www.bioparadigms.org/slc/ )。碳酸氢盐(HCO)转运蛋白 SLC4 家族由十个成员组成,根据其与钠(NBCe1、NBCe2、NBCn1、NBCn2、NDCBE)、氯(AE1、AE2、AE3)或硼酸(BTR1)的偶联情况进行分类。SLC4A9(AE4)的离子偶联仍存在争议。这些 SLC4 碳酸氢盐转运蛋白可能受细胞离子梯度、细胞膜电压和信号分子的控制,以维持关键的细胞和全身 pH(酸碱)平衡。即使血液 pH 值偏离正常范围(7.35-7.45)很小,也会产生严重后果。主要的是,Na 偶联的碳酸氢盐转运蛋白(NCBT)控制几乎所有活细胞中的细胞内 pH 值,维持生命所需的生物学 pH 值。此外,NCBT 在调节细胞体积和维持盐平衡以及酸碱当量的吸收和分泌方面也具有重要作用。由于其组织表达的多样性,NCBT 在病理生理学中具有作用,当它们的表达减少或遗传缺失时,这些作用在生理反应中变得明显。从经典的酸碱相关疾病到不一定与酸碱功能障碍相关的疾病,如癌症、青光眼或各种神经疾病,都可以看到生理 pH 值的变化。SLC4 转运蛋白的膜定位以及发现其结构生物学的最新进展使它们在疾病背景下成为可及和有吸引力的药物靶点。NCBT 在如此广泛的条件下的作用说明了通过调节这些转运蛋白的功能来治疗广泛的疾病状态的潜力,无论是通过抑制还是增强。