Scharschmidt B F, Stephens J E
Proc Natl Acad Sci U S A. 1981 Feb;78(2):986-90. doi: 10.1073/pnas.78.2.986.
Transport of sodium, chloride, and taurocholate was studied in primary cultures of adult rat hepatocytes incubated in a balanced electrolyte solution containing 150 mM NaCl, various concentrations of taurocholate, and (22)Na, (36)Cl, [(3)H]taurocholate, and 3-O-[(3)H]methyl-D-glucose. Lithium chloride, choline chloride, or Na(2)SO(4) and mannitol were substituted isotonically for NaCl in selected studies. The steady-state intracellular concentrations of exchangeable sodium and chloride averaged 6.5 mM and 30.1 mM, respectively. Ouabain reversibly increased intracellular sodium concentration. Chloride entry rate was about double that of sodium. Unlike sodium entry, chloride entry rate increased nonlinearly with increasing extracellular concentration. Taurocholate entry exhibited both saturable and nonsaturable components; the former accounting for virtually all taurocholate uptake at concentrations comparable to those found in vivo. Taurocholate was actively concentrated by the cultured cells, with the steady-state intracellular-to-extracellular concentration ratio decreasing from over 50 to about 1 as extracellular taurocholate concentration was increased from 10 muM to 4 mM. Both the saturable uptake component and concentrative taurocholate transport were virtually abolished by substitution of choline or lithium for sodium or by addition of ouabain. Taurocholate entry rate first increased in a sigmoid fashion and then decreased as extracellular sodium concentration was increased from 0 to 150 mM. Sodium entry rate increased in the presence of added taurocholate with an average of one sodium ion accompanying each taurocholate molecule into the cell. These findings indicate that sodium and chloride differ strikingly in their mechanism and rate of entry into cultured rat hepatocytes and in their intracellular concentration. Moreover, hepatocytes concentrate taurocholate by a sodium-coupled mechanism with an apparently equimolar transport stoichiometry.
在含有150 mM氯化钠、不同浓度牛磺胆酸盐以及(22)钠、(36)氯、[(3)H]牛磺胆酸盐和3 - O - [(3)H]甲基 - D - 葡萄糖的平衡电解质溶液中培养的成年大鼠肝细胞原代培养物中,研究了钠、氯和牛磺胆酸盐的转运。在选定的研究中,用氯化锂、氯化胆碱或硫酸钠和甘露醇等渗替代氯化钠。可交换钠和氯的稳态细胞内浓度分别平均为6.5 mM和30.1 mM。哇巴因可逆地增加细胞内钠浓度。氯的进入速率约为钠的两倍。与钠的进入不同,氯的进入速率随细胞外浓度增加呈非线性增加。牛磺胆酸盐的进入表现出饱和和非饱和成分;在与体内发现的浓度相当的浓度下,前者几乎占了所有牛磺胆酸盐的摄取。培养细胞可主动浓缩牛磺胆酸盐,随着细胞外牛磺胆酸盐浓度从10 μM增加到4 mM,稳态细胞内与细胞外浓度比从超过50降至约1。用胆碱或锂替代钠或添加哇巴因几乎消除了饱和摄取成分和牛磺胆酸盐的浓缩转运。随着细胞外钠浓度从0增加到150 mM,牛磺胆酸盐进入速率首先呈S形增加,然后下降。在添加牛磺胆酸盐的情况下,钠进入速率增加,平均每个牛磺胆酸盐分子伴随一个钠离子进入细胞。这些发现表明,钠和氯在进入培养的大鼠肝细胞的机制、速率以及细胞内浓度方面存在显著差异。此外,肝细胞通过钠偶联机制浓缩牛磺胆酸盐,其转运化学计量比明显为等摩尔。