Lang Z, Murlas C G
Lung Cell Biology Laboratories, Rush University, Chicago, IL 60612.
Am J Respir Cell Mol Biol. 1992 Sep;7(3):300-6. doi: 10.1165/ajrcmb/7.3.300.
Hypocholorous acid (HOCl) exposure of Calu-1 cells in situ leads to a relatively rapid and substantial decrease in whole cell neutral endopeptidase (NEP) activity that may result from the internalization of NEP from plasma membrane surfaces. To confirm this, and to assess the time course of changes in cell NEP after oxidant exposure and the potential influence of corticosteroid treatment on these, we evaluated Calu-1 NEP activity by high performance liquid chromatography and NEP-specific mRNA over the ensuing 48 h after HOCl in the presence or absence of 1 microM dexamethasone. Cells, grown to confluency in Dulbecco's modified Eagle's medium with 10% fetal bovine serum, were exposed for 5 min to 100 microM HOCl and then maintained in culture for 48 h thereafter. Before exposure, some cell plates were cooled to 4 degrees C and/or incubated for 5 min in 1 mM sodium azide. In some experiments, post-HOCl changes in NEP-specific mRNA in the presence or absence of dexamethasone were also evaluated using Northern blot analysis. We found that sodium azide at 4 degrees C totally blocked the effect of HOCl on Calu-1 NEP (n = 6). In the absence of sodium azide, NEP activity spontaneously recovered to preexposure levels within 24 h. This recovery occurred 6 h earlier in the presence of 1 microM dexamethasone. Furthermore, dexamethasone increased NEP activity at 24 and 48 h after HOCl. Northern blot analysis indicated that NEP-specific mRNA did not change during spontaneous recovery, but was increased by dexamethasone 24 h after HOCl.(ABSTRACT TRUNCATED AT 250 WORDS)
原位用次氯酸(HOCl)处理Calu - 1细胞会导致全细胞中性内肽酶(NEP)活性相对快速且显著降低,这可能是由于NEP从质膜表面内化所致。为证实这一点,并评估氧化剂暴露后细胞NEP活性变化的时间进程以及皮质类固醇处理对其的潜在影响,我们在存在或不存在1 microM地塞米松的情况下,通过高效液相色谱法和NEP特异性mRNA评估了HOCl处理后48小时内Calu - 1细胞的NEP活性。将细胞在含有10%胎牛血清的杜氏改良 Eagle培养基中培养至汇合,用100 microM HOCl处理5分钟,然后在培养中维持48小时。暴露前,一些细胞板冷却至4摄氏度和/或在1 mM叠氮化钠中孵育5分钟。在一些实验中,还使用Northern印迹分析评估了HOCl处理后在存在或不存在地塞米松的情况下NEP特异性mRNA的变化。我们发现4摄氏度的叠氮化钠完全阻断了HOCl对Calu - 1细胞NEP的作用(n = 6)。在不存在叠氮化钠的情况下,NEP活性在24小时内自发恢复到暴露前水平。在存在1 microM地塞米松的情况下,这种恢复提前6小时发生。此外,地塞米松在HOCl处理后24小时和48小时增加了NEP活性。Northern印迹分析表明,NEP特异性mRNA在自发恢复过程中没有变化,但在HOCl处理后24小时被地塞米松增加。(摘要截短至250字)