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鱼类红细胞中对容量敏感的牛磺酸转运

Volume-sensitive taurine transport in fish erythrocytes.

作者信息

Fincham D A, Wolowyk M W, Young J D

出版信息

J Membr Biol. 1987;96(1):45-56. doi: 10.1007/BF01869333.

Abstract

Taurine plays an important role in cell volume regulation in both vertebrates and invertebrates. Erythrocytes from two euryhaline fish species, the eel (Anguilla japonica) and the starry flounder (Platichthys stellatus) were found to contain high intracellular concentrations of this amino acid (approximately equal to 30 mmol per liter of cell water). Kinetic studies established that the cells possessed a saturable high-affinity Na+-dependent beta-amino-acid transport system which also required Cl- for activity (apparent Km (taurine) 75 and 80 microM; Vmax 0.85 and 0.29 mumol/g Hb per hr for eel (20 degrees C) and flounder cells (10 degrees C), respectively. This beta-system operated with an apparent Na+/Cl-/taurine coupling ratio of 2:1:1. A reduction in extracellular osmolarity, leading to an increase in cell volume, reversibly decreased the activity of the transporter. In contrast, low medium osmolarity stimulated the activity of a Na+-independent nonsaturable transport route selective for taurine, gamma-amino-n-butyric acid and small neutral amino acids, producing a net efflux of taurine from the cells. Neither component of taurine transport was detected in human erythrocytes. It is suggested that these functionally distinct transport routes participate in the osmotic regulation of intracellular taurine levels and hence contribute to the homeostatic regulation of cell volume. Volume-induced increases in Na+-independent taurine transport activity were suppressed by noradrenaline and 8-bromoadenosine-3', 5'-cyclic monophosphate, but unaffected by the anticalmodulin drug, pimozide.

摘要

牛磺酸在脊椎动物和无脊椎动物的细胞体积调节中发挥着重要作用。研究发现,两种广盐性鱼类——鳗鱼(日本鳗鲡)和星斑川鲽(星突江鲽)的红细胞中含有高浓度的这种氨基酸(约每升细胞水30毫摩尔)。动力学研究表明,这些细胞拥有一种可饱和的高亲和力Na⁺依赖性β-氨基酸转运系统,该系统的活性也需要Cl⁻(鳗鱼(20℃)和川鲽细胞(10℃)的表观Km(牛磺酸)分别为75和80微摩尔;Vmax分别为0.85和0.29微摩尔/克血红蛋白每小时)。这个β-系统的表观Na⁺/Cl⁻/牛磺酸偶联比为2:1:1。细胞外渗透压降低导致细胞体积增加时,转运体的活性会可逆性降低。相反,低渗透压介质会刺激一种对牛磺酸、γ-氨基丁酸和小中性氨基酸具有选择性的非Na⁺依赖性非饱和转运途径的活性,使牛磺酸从细胞中净流出。在人类红细胞中未检测到牛磺酸转运的任何成分。据推测这些功能不同的转运途径参与了细胞内牛磺酸水平的渗透调节,从而有助于细胞体积的稳态调节。体积诱导的非Na⁺依赖性牛磺酸转运活性增加受到去甲肾上腺素和8-溴腺苷-3',5'-环磷酸的抑制,但不受抗钙调蛋白药物匹莫齐特的影响。

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