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进一步研究人有机阴离子转运多肽 OATP1B1 和 OATP1B3 的电生成特性和 pH 敏感性。

Further characterization of the electrogenicity and pH sensitivity of the human organic anion-transporting polypeptides OATP1B1 and OATP1B3.

机构信息

Laboratory of Experimental Hepatology and Drug Targeting, University of Salamanca, Salamanca, Spain.

出版信息

Mol Pharmacol. 2011 Mar;79(3):596-607. doi: 10.1124/mol.110.069971. Epub 2010 Dec 20.

Abstract

Organic anion-transporting polypeptides (OATPs) are involved in the liver uptake of many endogenous and xenobiotic compounds, such as bile acids and drugs, respectively. Using Xenopus laevis oocytes and Chinese hamster ovary (CHO) cells expressing rat Oatp1a1, human OATP1B1, or OATP1B3, the sensitivity of these transporters to extracellular/intracellular pH (pHo/pHi) and changes in plasma membrane potential (ΔΨ) was investigated. In X. laevis oocytes, nonspecific plasma membrane permeability increased only at pHo below 4.5. Above this value, both using oocytes and CHO cells, extracellular acidification affected differently the specific transport of taurocholic acid (TCA) and estradiol 17β-d-glucuronide (E(2)17βG) by Oatp1a1 (stimulation), OATP1B1 (inhibition), and OATP1B3 (stimulation). Changes in substrate uptake in the presence of valinomycin (K(+)-ionophore), carbonyl cyanide 3-chlorophenylhydrazone and nigericin (protonophores), and amiloride (Na(+)/H(+)-inhibitor) and cation replacement in the medium were studied with fluorescent probes for measuring substrate uptake (cholylglycyl amidofluorescein) and changes in pHi (SNARF-4F) and ΔΨ [DilC(1)(5)]. The results suggest that activity of these three carriers is sodium/potassium-independent and affected differently by changes in pHo and ΔΨ: Oatp1a1 was confirmed to be an electroneutral anion exchanger, whereas the function of both OATP1B1 and OATP1B3 was markedly affected by the magnitude of ΔΨ. Moreover, electrophysiological measurements revealed the existence of a net anion influx associated to OATP1B1/OATP1B3-mediated transport of TCA, E(2)17βG, and estrone-3-sulfate. Furthermore, a leakage of Na(+) through OATP1B1 and OATP1B3, which is not coupled to substrate transport, was found. In conclusion, these results suggest that OATP1B1 and OATP1B3 are electrogenic transporters whose activity may be strongly affected under circumstances of displacement of local pH.

摘要

有机阴离子转运多肽 (OATPs) 参与许多内源性和外源性化合物的肝脏摄取,分别为胆汁酸和药物。使用非洲爪蟾卵母细胞和表达大鼠 Oatp1a1、人 OATP1B1 或 OATP1B3 的中国仓鼠卵巢 (CHO) 细胞,研究了这些转运体对细胞外/细胞内 pH (pHo/pHi) 和质膜电位 (ΔΨ) 变化的敏感性。在非洲爪蟾卵母细胞中,仅在 pHo 低于 4.5 时,非特异性质膜通透性才会增加。在该值以上,使用卵母细胞和 CHO 细胞,细胞外酸化以不同的方式影响牛磺胆酸 (TCA) 和雌二醇 17β-D-葡萄糖醛酸苷 (E(2)17βG) 的特定转运,Oatp1a1(刺激)、OATP1B1(抑制)和 OATP1B3(刺激)。用荧光探针测量底物摄取的变化(用于测量底物摄取的胆酰基甘氨酰氨荧光素)和 pHi(SNARF-4F)和 ΔΨ[DilC(1)(5)]变化,研究了在缬氨霉素(K(+)离子载体)、羰基氰化物 3-氯苯腙和尼可地尔(质子载体)以及阿米洛利(Na(+)/H(+)抑制剂)存在下和介质中阳离子替换的情况下的底物摄取。结果表明,这三种载体的活性与钠离子/钾离子无关,并且受到 pHo 和 ΔΨ 的变化的不同影响:Oatp1a1 被确认为电中性阴离子交换体,而 OATP1B1 和 OATP1B3 的功能则受到 ΔΨ 幅度的显著影响。此外,电生理学测量显示与 TCA、E(2)17βG 和雌酮-3-硫酸盐的 OATP1B1/OATP1B3 介导的转运相关联存在净阴离子内流。此外,发现 OATP1B1 和 OATP1B3 存在不与底物转运偶联的 Na(+) 渗漏。总之,这些结果表明 OATP1B1 和 OATP1B3 是电致性转运体,其活性在局部 pH 置换的情况下可能会受到强烈影响。

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