Department of Physiology, Center for Research and Advanced Studies, 07300 Mexico DF, Mexico.
Proc Natl Acad Sci U S A. 2010 Jun 22;107(25):11387-92. doi: 10.1073/pnas.1000500107. Epub 2010 Jun 4.
Epithelial cells treated with high concentrations of ouabain (e.g., 1 microM) retrieve molecules involved in cell contacts from the plasma membrane and detach from one another and their substrates. On the basis of this observation, we suggested that ouabain might also modulate cell contacts at low, nontoxic levels (10 or 50 nM). To test this possibility, we analyzed its effect on a particular type of cell-cell contact: the tight junction (TJ). We demonstrate that at concentrations that neither inhibit K(+) pumping nor disturb the K(+) balance of the cell, ouabain modulates the degree of sealing of the TJ as measured by transepithelial electrical resistance (TER) and the flux of neutral 3 kDa dextran (J(DEX)). This modulation is accompanied by changes in the levels and distribution patterns of claudins 1, 2, and 4. Interestingly, changes in TER, J(DEX), and claudins behavior are mediated through signal pathways containing ERK1/2 and c-Src, which have distinct effects on each physiological parameter and claudin type. These observations support the theory that at low concentrations, ouabain acts as a modulator of cell-cell contacts.
用高浓度哇巴因(例如 1μM)处理的上皮细胞会从质膜中回收参与细胞接触的分子,并彼此分离以及与它们的基质分离。基于这一观察结果,我们认为哇巴因也可能在低毒水平(10 或 50 nM)下调节细胞接触。为了验证这种可能性,我们分析了它对一种特殊类型的细胞-细胞接触:紧密连接(TJ)的影响。我们证明,在既不抑制 K+泵又不扰乱细胞 K+平衡的浓度下,哇巴因调节 TJ 的封闭程度,这可以通过跨上皮电阻(TER)和中性 3 kDa 葡聚糖(J(DEX))通量来衡量。这种调节伴随着 Claudin 1、2 和 4 的水平和分布模式的变化。有趣的是,TER、J(DEX)和 Claudin 行为的变化是通过包含 ERK1/2 和 c-Src 的信号途径介导的,这些途径对每个生理参数和 Claudin 类型都有不同的影响。这些观察结果支持了这样一种理论,即在低浓度下,哇巴因作为细胞-细胞接触的调节剂发挥作用。