Okech Bernard A, Meleshkevitch Ella A, Miller Melissa M, Popova Lyudmila B, Harvey William R, Boudko Dmitri Y
The Whitney Laboratory for Marine Bioscience, University of Florida, 9505 Ocean Shore Boulevard, St Augustine, FL 3208, USA.
J Exp Biol. 2008 May;211(Pt 10):1594-602. doi: 10.1242/jeb.017244.
The nutrient amino acid transporter (NAT) subfamily is the largest subdivision of the sodium neurotransmitter symporter family (SNF; also known as SLC6; HUGO). There are seven members of the NAT population in the African malaria mosquito Anopheles gambiae, two of which, AgNAT6 and AgNAT8, preferably transport indole- and phenyl-branched substrates, respectively. The relative expression and distribution of these aromatic NATs were examined with transporter-specific antibodies in Xenopus oocytes and mosquito larval alimentary canal, representing heterologous and tissue expression systems, respectively. NAT-specific aromatic-substrate-induced currents strongly corresponded with specific accumulation of both transporters in the plasma membrane of oocytes. Immunolabeling revealed elevated expressions of both transporters in specific regions of the larval alimentary canal, including salivary glands, cardia, gastric caeca, posterior midgut and Malpighian tubules. Differences in relative expression densities and spatial distribution of the transporters were prominent in virtually all of these regions, suggesting unique profiles of the aromatic amino acid absorption. For the first time reversal of the location of a transporter between apical and basal membranes was identified in posterior and anterior epithelial domains corresponding with secretory and absorptive epithelial functions, respectively. Both aromatic NATs formed putative homodimers in the larval gut whereas functional monomers were over-expressed heterologously in Xenopus oocytes. The results unequivocally suggest functional synergy between substrate-specific AgNAT6 and AgNAT8 in intracellular absorption of aromatic amino acids. More broadly, they suggest that the specific selectivity, regional expression and polarized membrane docking of NATs represent key adaptive traits shaping functional patterns of essential amino acid absorption in the metazoan alimentary canal and other tissues.
营养氨基酸转运体(NAT)亚家族是钠神经递质同向转运体家族(SNF;也称为SLC6;人类基因组组织)中最大的细分家族。在非洲疟蚊冈比亚按蚊中,NAT群体有七个成员,其中两个成员,即AgNAT6和AgNAT8,分别优先转运吲哚和苯基支链底物。分别在非洲爪蟾卵母细胞和蚊虫幼虫消化道中,使用转运体特异性抗体检测了这些芳香族NAT的相对表达和分布,二者分别代表异源表达系统和组织表达系统。NAT特异性芳香族底物诱导的电流与两种转运体在卵母细胞质膜中的特异性积累密切相关。免疫标记显示,这两种转运体在幼虫消化道的特定区域,包括唾液腺、贲门、胃盲囊、中肠后部和马氏管中表达升高。在几乎所有这些区域,转运体的相对表达密度和空间分布差异都很显著,这表明芳香族氨基酸吸收具有独特的特征。首次在分别与分泌性和吸收性上皮功能相对应的后上皮域和前上皮域中,发现了转运体在顶端膜和基底膜之间位置的逆转。两种芳香族NAT在幼虫肠道中形成了假定的同二聚体,而功能性单体在非洲爪蟾卵母细胞中异源过表达。结果明确表明,底物特异性的AgNAT6和AgNAT8在芳香族氨基酸的细胞内吸收中存在功能协同作用。更广泛地说,它们表明NAT的特异性选择性、区域表达和极化膜对接代表了塑造后生动物消化道和其他组织中必需氨基酸吸收功能模式的关键适应性特征。