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Membrane potential difference and intracellular cation concentrations in human placental trophoblast cells in culture.

机译:培养的人胎盘滋养层细胞膜电位差和细胞内阳离子浓度

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摘要

1. The electrochemical gradients for Na+ and K+ were assessed in a cell culture model of trophoblast differentiation. 2. Membrane potential difference (Em), intracellular water and Na+ and K+ contents were measured in choriocarcinoma cells (JAr cell line; 96% of which are undifferentiated trophoblast cells) and in mononucleate and multinucleate (differentiated) cytotrophoblast cells isolated from the human placenta at term. 3. There was a significant fall in Em from -57 mV in JAr cells, to -48 and -40 mV in mono-and multinucleate cytotrophoblast cells, respectively. Treatment with ouabain (1 mM for 15 min) depolarized the JAr cell membrane by 15 mV but did not affect cytotrophoblast cell membrane potential. 4. Intracellular K+ concentration was similar in JAr, mono- and multinucleate cytotrophoblast cells but Na+ concentration was higher in mononucleate cytotrophoblast cells compared with JAr cells. 5. Ouabain treatment (3 mM for 15 min) caused a small increase (4.5%) in cell water in mononucleate cytotrophoblast cells but lowered K+ (approximately 30%) and increased Na+ concentration (approximately 125%) in all the trophoblast cells studied. 6. The K+ equilibrium potential (EK) was more negative than Em in all cells and the difference between EK and Em was smaller in JAr cells (-25 mV) than in mono- and multinucleate cytotrophoblast cells (-33 and -43 mV, respectively). 7. The Na+ equilibrium potential (ENa) was positive in the trophoblast cells and the difference between ENa and Em was 122, 100 and 100 mV in JAr, mono- and multinucleate cytotrophoblast cells, respectively. 8. These results suggest that the electrochemical gradient for K+ is affected by the stage of trophoblast cell differentiation. In contrast, the electrochemical gradient for Na+ is similar in mono- and multinucleate cytotrophoblast cells.
机译:1.在滋养细胞分化的细胞培养模型中评估Na +和K +的电化学梯度。 2.测量绒毛膜癌细胞(JAr细胞系;其中96%为未分化的滋养层细胞)以及从人胎盘分离的单核和多核(分化)细胞滋养层细胞的膜电位差(Em),细胞内水以及Na +和K +含量在学期。 3.在Jar细胞中,Em分别从-57 mV显着下降,在单核和多核细胞滋养层细胞中,Em分别下降至-48和-40 mV。用哇巴因(1 mM进行15分钟)处理可使JAr细胞膜去极化15 mV,但不影响细胞滋养层细胞膜电位。 4. JAr,单核和多核细胞滋养层细胞的细胞内K +浓度相似,但单核细胞滋养层细胞中Na +浓度高于JAr细胞。 5.哇巴因处理(3 mM,持续15分钟)使单核细胞滋养层细胞的细胞水略有增加(4.5%),但所有研究的滋养层细胞中的K +降低(约30%),Na +浓度升高(约125%)。 6.在所有细胞中,K +平衡电位(EK)均比Em负,并且JAr细胞(-25 mV)的EK和Em之间的差异小于单核和多核滋养层细胞(-33和-43 mV,分别)。 7.在滋养层细胞中,Na +平衡电位(ENa)为正,在JAr,单核和多核滋养层细胞中,ENa和Em的差分别为122、100和100 mV。 8.这些结果表明,K +的电化学梯度受滋养层细胞分化阶段的影响。相反,Na +的电化学梯度在单核和多核滋养细胞中相似。

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