Elias Nael, Rafii Bijan, Rahman Muhammad, Otulakowski Gail, Cutz Ernest, O'Brodovich Hugh
Program in Lung Biology, Hospital for Sick Children Research Institute, Toronto, canada.
Am J Physiol Lung Cell Mol Physiol. 2007 Sep;293(3):L537-45. doi: 10.1152/ajplung.00373.2006. Epub 2007 May 18.
Edema fluid (EF) increases epithelial Na(+) transport by rat fetal distal lung epithelia (FDLE) and induces net lung fluid absorption in fetal mouse lung explants [Rafii B, Gillie DJ, Sulowski C, Hannam V, Cheung T, Otulakowski G, Barker PM, O'Brodovich H. J Physiol (Lond) 544: 537-548, 2002]. We now show that EF increases fluid absorption across monolayers of rat FDLE in a dose-dependent manner. To study the role of subunits of the epithelial Na(+) channel (ENaC) in the phenomena, we cultured explants from the distal lungs of 16-day gestational age wild-type (WT) or alpha-, beta-, or gamma-ENaC knockout or heterozygote (HT) mice. WT explants cultured in media continuously expanded over time as a result of net fluid secretion. In contrast, when explants were exposed to EF for 24 h, net fluid absorption occurred. EF-exposed explants had normal histology, but marked changes were seen after Triton X-100 or staurosporine exposure. Transmission electron microscopy showed EF promoted lamellar body formation and abundant surfactant in the explants' lumens. EF-induced changes in explant size were similar in alpha-ENaC knockout, WT, and HT littermate fetal lung explants (P > 0.05). In contrast, EF's effect was attenuated in beta- and gamma-ENaC knockouts (P < 0.05) vs. WT and HT littermate fetal lung explants. EF exposure slightly decreased or had no effect on mRNA levels for alpha-ENaC in various mouse genotypes but decreased expression of beta- and gamma-ENaC subunit mRNAs (P < 0.01) across all genotype groups. We conclude that beta- and gamma-, but not alpha-, ENaC subunits are essential for EF to exert its maximal effect on net fluid absorption by distal lung epithelia.
水肿液(EF)可增加大鼠胎儿远端肺上皮细胞(FDLE)的上皮钠(Na⁺)转运,并诱导胎鼠肺组织块出现肺液净吸收[拉菲·B、吉利·DJ、苏洛斯基·C、汉南·V、张·T、奥图拉科夫斯基·G、巴克·PM、奥布罗多维奇·H。《生理学杂志》(伦敦)544:537 - 548,2002年]。我们现在发现,EF以剂量依赖的方式增加大鼠FDLE单层细胞的液体吸收。为了研究上皮钠通道(ENaC)亚基在这一现象中的作用,我们培养了来自妊娠16天的野生型(WT)或α -、β - 或γ - ENaC基因敲除或杂合子(HT)小鼠远端肺的组织块。WT组织块在培养基中培养时,由于液体净分泌,随着时间推移持续膨胀。相比之下,当组织块暴露于EF 24小时时,出现了液体净吸收。暴露于EF的组织块组织学正常,但在暴露于曲拉通X - 100或星形孢菌素后出现了明显变化。透射电子显微镜显示EF促进了板层小体形成以及组织块管腔内丰富的表面活性剂产生。EF诱导的组织块大小变化在α - ENaC基因敲除、WT和HT同窝胎鼠肺组织块中相似(P > 0.05)。相比之下,与WT和HT同窝胎鼠肺组织块相比,EF在β - 和γ - ENaC基因敲除组织块中的作用减弱(P < 0.05)。EF暴露在各种小鼠基因型中对α - ENaC的mRNA水平略有降低或无影响,但在所有基因型组中均降低了β - 和γ - ENaC亚基mRNA的表达(P < 0.01)。我们得出结论,β - 和γ -,而非α -,ENaC亚基对于EF对远端肺上皮细胞液体净吸收发挥最大作用至关重要。