Holopainen I, Kontro P, Frey H J, Oja S S
J Neurosci Res. 1983;10(1):83-92. doi: 10.1002/jnr.490100110.
Uptake of [3H]taurine, [35S]hypotaurine, and [3H] gamma-aminobutyric acid (GABA) was studied in neuroblastoma C1300 cells in Krebs-Ringer-Hepes-glucose medium (pH 7.4). The uptakes consisted of nonsaturable penetration (taurine and hypotaurine) and two saturable transport components: high affinity for taurine, hypotaurine, and GABA and low affinity for hypotaurine and GABA. The affinity of the high-affinity uptake was highest for hypotaurine but the transport capacity was greatest for taurine. GABA uptake was almost abolished by taurine and hypotaurine. Hypotaurine also strongly inhibited taurine uptake, whereas GABA had only a moderate inhibitory effect on taurine and hypotaurine uptakes. The mutual inhibition suggests that these amino acids use the same transport sites when entering the cells.
在含有 Krebs-Ringer-Hepes-葡萄糖的培养基(pH 7.4)中,对神经母细胞瘤 C1300 细胞摄取 [3H] 牛磺酸、[35S] 次牛磺酸和 [3H]γ-氨基丁酸(GABA)进行了研究。摄取包括非饱和渗透(牛磺酸和次牛磺酸)以及两个饱和转运成分:对牛磺酸、次牛磺酸和 GABA 具有高亲和力,对次牛磺酸和 GABA 具有低亲和力。高亲和力摄取对次牛磺酸的亲和力最高,但对牛磺酸的转运能力最大。牛磺酸和次牛磺酸几乎完全抑制了 GABA 的摄取。次牛磺酸也强烈抑制牛磺酸的摄取,而 GABA 对牛磺酸和次牛磺酸的摄取仅具有中等抑制作用。相互抑制表明这些氨基酸在进入细胞时使用相同的转运位点。