Marin J J, Serrano M A, el-Mir M Y, Eleno N, Boyd C A
Department of Physiology and Pharmacology, University of Salamanca, Spain.
Gastroenterology. 1990 Nov;99(5):1431-8. doi: 10.1016/0016-5085(90)91172-3.
The aim of this work was to investigate the first step in the vectorial translocation of bile acids from the fetus to the mother, which is the transfer across the basal (i.e., fetal-facing) plasma membrane of the trophoblast. Thus, the uptake of [14C]taurocholate by basal plasma membrane vesicles obtained from normal human term placentas was studied. Taurocholate retention into vesicles was studied using a rapid filtration technique that was modified to reduce the taurocholate binding to the filters and to the external surface of the vesicles. Using 100 mumol/L substrate, the membrane vesicles showed a temperature-dependent, Na(+)-independent transport of taurocholate into an osmotically reactive intravesicular space. The initial rate of taurocholate influx in the presence of 100 mmol/L KNO3 followed saturation kinetics (apparent Km for taurocholate = 670 +/- 128 mumol/L; Vmax = 1.86 +/- 0.28 nmol/mg protein.60 s at 37 degrees C). Over the 6.9-7.9 pH range neither internal nor external pH nor inward nor outward proton gradients affected the uptake of taurocholate. When the electrical potential difference across the basal membrane was manipulated by external anion replacement (Cl-, SCN-, SO4(2-), or NO3-) or by valinomycin-induced K(+)-diffusion potential (vesicle inside negative), taurocholate uptake was not significantly modified. Taurocholate uptake was cis-inhibited in the presence of 1 mmol/L glycocholate, 0.5 mmol/L 4,4'-diisothiocyanostilbene-2,2'-disulfonate and 0.5 mmol/L sulfobromophthalein. However, 1 mmol/L probenecid or 0.5 mmol/L p-aminohippurate had no effect. Moreover, preloading the vesicles with 100 mmol/L HCO3- (but not with 100 mmol/L Cl- or 50 mmol/L SO4(2-) induced a significant enhancement in the initial rate of taurocholate uptake. In summary, these findings provide strong evidence for the presence of an electroneutral transport system for taurocholate in the basal plasma membrane of human chorionic trophoblast. They also suggest that this is likely to be an anion-exchange system.
这项工作的目的是研究胆汁酸从胎儿向母体进行矢量转运的第一步,即跨越滋养层基底(即面向胎儿的)质膜的转运。因此,研究了从正常足月人胎盘获得的基底质膜囊泡对[14C]牛磺胆酸盐的摄取。使用一种经过改进的快速过滤技术研究牛磺胆酸盐在囊泡中的保留情况,该技术可减少牛磺胆酸盐与滤器以及囊泡外表面的结合。使用100μmol/L的底物时,膜囊泡显示出牛磺胆酸盐向渗透活性囊泡内空间的温度依赖性、不依赖Na(+)的转运。在100mmol/L KNO3存在下,牛磺胆酸盐流入的初始速率遵循饱和动力学(牛磺胆酸盐的表观Km = 670±128μmol/L;Vmax = 1.86±0.28nmol/mg蛋白质.60s,37℃)。在6.9 - 7.9的pH范围内,内部或外部pH以及内向或外向质子梯度均不影响牛磺胆酸盐的摄取。当通过外部阴离子置换(Cl-、SCN-、SO4(2-)或NO3-)或缬氨霉素诱导的K(+)扩散电位(囊泡内部为负)来操纵基底膜上的电位差时,牛磺胆酸盐的摄取没有明显改变。在1mmol/L甘氨胆酸盐、0.5mmol/L 4,4'-二异硫氰基芪-2,2'-二磺酸盐和0.5mmol/L磺溴酞存在时,牛磺胆酸盐的摄取受到顺式抑制。然而,1mmol/L丙磺舒或0.5mmol/L对氨基马尿酸没有影响。此外,用100mmol/L HCO3-(但不用100mmol/L Cl-或50mmol/L SO4(2-))预加载囊泡会导致牛磺胆酸盐摄取的初始速率显著提高。总之,这些发现为人类绒毛膜滋养层基底质膜中存在牛磺胆酸盐的电中性转运系统提供了有力证据。它们还表明这可能是一个阴离子交换系统。