首页> 美国卫生研究院文献>The Journal of Physiology >Activation of a novel organic solute transporter in mammalian red blood cells.
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Activation of a novel organic solute transporter in mammalian red blood cells.

机译:哺乳动物红细胞中新型有机溶质转运蛋白的活化。

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摘要

1. Suspending human red blood cells in isotonic sucrose (low ionic strength, LIS) medium induces a significant increase in membrane transport of glutamine, glutamate, lactate, histidine, taurine, glycine, serine, choline and carnitine but not sorbitol or sucrose. 2. Progressive lowering of ionic strength by sucrose or NaCl replacement gave a similar activation profile for taurine influx as found earlier for residual K+(86Rb+) flux. 3. The induced taurine transport could be measured as enhanced influx and efflux. Influx was linear with external concentration up to 10 mM, largely insensitive to alteration in cell volume, and did not vary with red blood cell age. 4. Unlike previous results for residual K+ transport, altering transmembrane potential with gluconate or glucuronate media led to an increase in taurine influx similar to that observed in LIS media. Varying medium pH confirmed the effect was not due to alteration in pH. 5. The LIS-induced flux was sensitive to a variety of 'classical' anion transport inhibitors in the order of potency DNDS, DIDS, NPPB, DIOA, niflumic acid, furosemide (frusemide), glibenclamide, nitrendipine and bumetanide. 6. The taurine flux showed a temperature dependence similar to that of the LIS-induced residual K+ flux. High hydrostatic pressure (40 MPa), however, inhibited taurine flux but stimulated residual K+ influx in LIS media. 7. A significant enhanced taurine flux could be demonstrated in red blood cells of other species, including horse, cattle, pig and high and low potassium type sheep. 8. It is concluded that lowering ionic strength activates a transport pathway for organic molecules sharing some similarities with background Cl- channels and LIS-induced residual K+ fluxes. In the latter context, however, there are certain significant differences (effect of transmembrane potential; volume; pressure sensitivity; species distribution) which may be important, and the unequivocal identity of the two transport processes remains to be confirmed.
机译:1.在等渗蔗糖(低离子强度,LIS)培养基中悬浮的人红细胞引起谷氨酰胺,谷氨酸,乳酸,组氨酸,牛磺酸,甘氨酸,丝氨酸,胆碱和肉碱的膜运输显着增加,但山梨醇或蔗糖则没有。 2.蔗糖或NaCl替代物使离子强度逐渐降低,对牛磺酸流入产生了类似的活化曲线,这与先前对残留K +(86Rb +)助熔剂的发现相似。 3.诱导的牛磺酸转运可以测量为增强的流入和流出。流入量呈线性关系,外部浓度最高为10 mM,对细胞体积的变化不敏感,并且不随红细胞年龄而变化。 4.与以前的残留K +转运结果不同,用葡萄糖酸或葡萄糖醛酸介质改变跨膜电位可导致牛磺酸流入增加,类似于在LIS介质中观察到的情况。不同的培养基pH值证实效果不是由于pH值的改变。 5. LIS诱导的通量对各种“经典”阴离子转运抑制剂敏感,依次为DNDS,DIDS,NPPB,DIOA,尼氟酸,呋塞米(氟磺胺),格列本脲,硝苯地平和布美他尼。 6.牛磺酸通量显示出与LIS诱导的残留K +通量相似的温度依赖性。然而,高静水压(40 MPa)抑制了牛磺酸通量,但刺激了LIS介质中残留的K +流入。 7.牛,牛,猪以及高钾和低钾型绵羊等其他物种的红细胞中,牛磺酸的通量也可显着提高。 8.结论是,降低离子强度会激活有机分子与背景Cl-通道和LIS诱导的残留K +通量具有某些相似性的传输途径。然而,在后一种情况下,可能存在重要的某些显着差异(跨膜电位的影响;体积;压力敏感性;物种分布),两个运输过程的明确身份仍有待确认。

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