Kemp P J, Borok Z, Kim K J, Lubman R L, Danto S I, Crandall E D
School of Biomedical Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom.
Am J Physiol. 1999 Dec;277(6):C1058-65. doi: 10.1152/ajpcell.1999.277.6.C1058.
Using the patch-clamp technique, we studied the effects of epidermal growth factor (EGF) on whole cell and single channel currents in adult rat alveolar epithelial type II cells in primary culture in the presence or absence of EGF for 48 h. In symmetrical sodium isethionate solutions, EGF exposure caused a significant increase in the type II cell whole cell conductance. Amiloride (10 microM) produced approximately 20-30% inhibition of the whole cell conductance in both the presence and absence of EGF, such that EGF caused the magnitude of the amiloride-sensitive component to more than double. Northern analysis showed that alpha-, beta- and gamma-subunits of rat epithelial Na(+) channel (rENaC) steady-state mRNA levels were all significantly decreased by EGF. At the single channel level, all active inside-out patches demonstrated only 25-pS channels that were amiloride sensitive and relatively nonselective for cations (P(Na(+))/P(K(+)) approximately 1.0:0.48). Although the biophysical characteristics (conductance, open-state probability, and selectivity) of the channels from EGF-treated and untreated cells were essentially identical, channel density was increased by EGF; the modal channel per patch was increased from 1 to 2. These findings indicate that EGF increases expression of nonselective, amiloride-sensitive cation channels in adult alveolar epithelial type II cells. The contribution of rENaC to the total EGF-dependent cation current under these conditions is quantitatively less important than that of the nonselective cation channels in these cells.
我们运用膜片钳技术,研究了表皮生长因子(EGF)对原代培养的成年大鼠Ⅱ型肺泡上皮细胞全细胞电流和单通道电流的影响。在有无EGF的情况下培养48小时后,在对称的羟乙基磺酸钠溶液中,暴露于EGF会导致Ⅱ型细胞全细胞电导显著增加。在有和没有EGF的情况下,氨氯吡咪(10微摩尔)对全细胞电导的抑制作用约为20%-30%,因此EGF使氨氯吡咪敏感成分的幅度增加了一倍多。Northern分析表明,大鼠上皮钠通道(rENaC)的α、β和γ亚基的稳态mRNA水平均因EGF而显著降低。在单通道水平上,所有活性的内向外膜片仅显示25皮安的通道,这些通道对氨氯吡咪敏感且对阳离子相对无选择性(P(Na+)/P(K+)约为1.0:0.48)。尽管来自EGF处理和未处理细胞的通道的生物物理特性(电导、开放概率和选择性)基本相同,但EGF增加了通道密度;每个膜片的模态通道从1个增加到2个。这些发现表明,EGF增加了成年Ⅱ型肺泡上皮细胞中非选择性、氨氯吡咪敏感阳离子通道的表达。在这些条件下,rENaC对总EGF依赖性阳离子电流的贡献在数量上不如这些细胞中的非选择性阳离子通道重要。