Wang Su, Meng Fei, Xu Jingyuan, Gu Yuchun
Department of Physiology, University of Birmingham, Edgbaston, B15 2TT, UK.
J Membr Biol. 2009 Jan;227(2):77-85. doi: 10.1007/s00232-008-9145-1. Epub 2009 Jan 3.
Direct effects on epithelial Na+ channels (ENaC) activity by lipids, e.g., arachidonic acid (AA), eicosatetraynoic acid (ETYA), linoleic acid (LA), stearic acid (SA), hydroxyeicosatetraenoic acid (HETE), 11,12-epoxyeicosatrienoic acid (EET), (PGF2), and (PGE2), in cultured mouse cortical collecting duct (M1) cells were clarified by using single-channel recordings in this study. In a cell-attached recording, a bath application of 10 microM AA significantly reduced the ENaC open probability (NPo), whereas 10 microM ETYA or 5 microM LA only induced a slight inhibition. The inside-out recording as a standard protocol was thereafter performed to examine effects of these lipids on ENaC activity. Within 10 min after the formation of the inside-out configuration, the NPo of ENaC in cultured mouse cortical collecting duct (M1) cells remained relatively constant. Application of ETYA or LA or SA exhibited a similar inhibition on the channel NPo when applied to the extracellular side, suggesting that fatty acids could exert a nonspecific inhibition on ENaC activity. 11,12-EET, a metabolite of AA via the cytochrome P450 epoxygenase pathway, significantly inhibited the ENaC NPo, whereas 20-HETE, a metabolite of AA via the hydroxylase pathway, only caused a small inhibition of the ENaC NPo, to a similar degree as that seen with ETYA and LA. However, both PGE2 and PGF2alpha significantly enhanced the ENaC NPo. These results suggest that fatty acids exert a nonspecific effect on ENaC activity due to the interaction between the channel proximity and the lipid. The opposite effects of 11,12-EET and prostaglandin (PG) implicate different mechanisms in regulation of ENaC activity by activation of epoxygenase and cyclooxygenase.
本研究通过单通道记录明确了脂质(如花生四烯酸(AA)、二十碳四炔酸(ETYA)、亚油酸(LA)、硬脂酸(SA)、羟基花生四烯酸(HETE)、11,12-环氧二十碳三烯酸(EET)、前列腺素F2(PGF2)和前列腺素E2(PGE2))对培养的小鼠皮质集合管(M1)细胞上皮钠通道(ENaC)活性的直接影响。在细胞贴附式记录中,向浴槽中加入10微摩尔的AA可显著降低ENaC的开放概率(NPo),而10微摩尔的ETYA或5微摩尔的LA仅引起轻微抑制。此后,采用标准的内面向外式记录方法来研究这些脂质对ENaC活性的影响。在形成内面向外式构型后的10分钟内,培养的小鼠皮质集合管(M1)细胞中ENaC的NPo保持相对稳定。当将ETYA、LA或SA应用于细胞外侧时,对通道NPo表现出类似的抑制作用,这表明脂肪酸可能对ENaC活性产生非特异性抑制。11,12-EET是AA经细胞色素P450环氧化酶途径的代谢产物,可显著抑制ENaC的NPo,而20-HETE是AA经羟化酶途径的代谢产物,仅对ENaC的NPo产生较小的抑制作用,其程度与ETYA和LA相似。然而,PGE2和PGF2α均显著提高了ENaC的NPo。这些结果表明,由于通道附近与脂质之间的相互作用,脂肪酸对ENaC活性产生非特异性影响。11,12-EET与前列腺素(PG)的相反作用暗示了通过环氧化酶和环氧合酶激活对ENaC活性进行调节的不同机制。