Compr Physiol. 2014 Jan;4(1):367-403. doi: 10.1002/cphy.c130028.
Amino acids are the building blocks of proteins and key intermediates in the synthesis of biologically important molecules, as well as energy sources, neurotransmitters, regulators of cellular metabolism, etc. The efficient recovery of amino acids from the primary filtrate is a well-conserved key role of the kidney proximal tubule. Additionally, renal metabolism participates in the whole body disposition of amino acids. Therefore, a wide array of axially heterogeneously expressed transporters is localized on both epithelial membranes. For transepithelial transport, luminal uptake, which is carried out mainly by active symporters, is coupled with a mostly passive basolateral efflux. Many transporters require partner proteins for appropriate localization, or to modulate transporter activity, and/or increase substrate supply. Interacting proteins include cell surface antigens (CD98), endoplasmic reticulum proteins (GTRAP3-18 or 41), or enzymes (ACE2 and aminopeptidase N). In the past two decades, the molecular identification of transporters has led to significant advances in our understanding of amino acid transport and aminoacidurias arising from defects in renal transport. Furthermore, the three-dimensional crystal structures of bacterial homologues have been used to yield new insights on the structure and function of mammalian transporters. Additionally, transgenic animal models have contributed to our understanding of the role of amino acid transporters in the kidney and other organs and/or at critical developmental stages. Progress in elucidation of the renal contribution to systemic amino acid homeostasis requires further integration of kinetic, regulatory, and expression data of amino acid transporters into our understanding of physiological regulatory networks controlling metabolism.
氨基酸是蛋白质的组成部分,也是生物重要分子合成的关键中间产物,同时也是能量来源、神经递质、细胞代谢调节剂等。从原滤液中高效回收氨基酸是肾脏近端小管的一个很好的保守关键作用。此外,肾脏代谢参与了氨基酸在全身的分布。因此,广泛的轴向上异质表达的转运体定位于上皮细胞膜的两侧。对于跨上皮转运,主要通过主动转运体进行的腔侧摄取与主要为被动的基底外侧外排相偶联。许多转运体需要伴侣蛋白来进行适当的定位,或者调节转运体的活性,和/或增加底物的供应。相互作用的蛋白包括细胞表面抗原(CD98)、内质网蛋白(GTRAP3-18 或 41)或酶(ACE2 和氨肽酶 N)。在过去的二十年中,转运体的分子鉴定使我们对氨基酸转运和肾脏转运缺陷引起的氨基酸尿症的理解有了显著的进展。此外,细菌同源物的三维晶体结构被用于获得关于哺乳动物转运体的结构和功能的新见解。此外,转基因动物模型有助于我们了解氨基酸转运体在肾脏和其他器官中的作用,以及在关键发育阶段的作用。阐明肾脏对全身氨基酸稳态的贡献需要将氨基酸转运体的动力学、调节和表达数据进一步整合到我们对控制代谢的生理调节网络的理解中。