Dussaule J C, Stefanski A, Béa M L, Ronco P, Ardaillou R
Institut National de la Santé et de la Recherche Médicale 64, Hôpital Tenon, Paris, France.
Am J Physiol. 1993 Jan;264(1 Pt 2):F45-52. doi: 10.1152/ajprenal.1993.264.1.F45.
In addition to biological and clearance receptors for atrial natriuretic factor (ANF), cultured vascular smooth muscle cells (VSMC) from the rabbit renal cortex possess ectoenzymes degrading this hormone. We examined whether neutral endopeptidase (NEP) was implicated in this process. The presence of NEP in VSMC was demonstrated as follows. 1) NEP activity measured from the hydrolysis of a synthetic substrate by intact cells cultured in a medium containing 10% fetal calf serum was 1,609 +/- 65 pmol.min-1 x mg-1 [surface localization of the enzyme was confirmed by low activity (4% of total) in the cytosol; release of NEP activity in the medium was negligible]; 2) a monoclonal antibody directed against rabbit NEP specifically stained VSMC membranes; and 3) mRNA from VSMC hybridized a NEP cDNA probe with a single band as shown by Northern blot analysis. The role of NEP in ANF catabolism was demonstrated by incubating 125I-ANF or unlabeled ANF for increasing periods of time with VSMC in the presence of thiorphan (1-100 microM). Intact hormone estimated by trichloroacetic acid precipitation or radio-immunoassay, respectively, increased markedly compared with control in the presence of this specific inhibitor of NEP. NEP activity was stimulated (x1.6) in quiescent VSMC deprived from serum during 3 days. This effect was dose dependent and was not observed with creatine kinase activity measured as control. NEP expression at the cell surface estimated by sorting of immunostained cells was also increased in the absence of serum. Northern blot analysis showed increases in the mRNA band of NEP with increasing periods of serum deprivation.(ABSTRACT TRUNCATED AT 250 WORDS)
除了心房利钠因子(ANF)的生物和清除受体外,来自兔肾皮质的培养血管平滑肌细胞(VSMC)还具有降解这种激素的胞外酶。我们研究了中性内肽酶(NEP)是否参与了这一过程。VSMC中NEP的存在如下所示。1)在含有10%胎牛血清的培养基中培养的完整细胞,通过合成底物水解测得的NEP活性为1,609±65 pmol·min⁻¹·mg⁻¹[通过胞质溶胶中低活性(占总量的4%)证实了该酶的表面定位;培养基中NEP活性的释放可忽略不计];2)一种针对兔NEP的单克隆抗体特异性地对VSMC膜进行了染色;3)如Northern印迹分析所示,VSMC的mRNA与NEP cDNA探针杂交产生一条单带。通过在存在硫磷酰胺(1 - 100 microM)的情况下,将¹²⁵I - ANF或未标记的ANF与VSMC孵育不同时间,证明了NEP在ANF分解代谢中的作用。在这种NEP特异性抑制剂存在的情况下,分别通过三氯乙酸沉淀或放射免疫测定法估算的完整激素与对照相比显著增加。在3天内血清饥饿的静止VSMC中,NEP活性受到刺激(增加了1.6倍)。这种效应呈剂量依赖性,而作为对照测量的肌酸激酶活性未观察到这种效应。通过对免疫染色细胞进行分选估算的细胞表面NEP表达在无血清时也增加。Northern印迹分析显示,随着血清饥饿时间的延长,NEP的mRNA条带增加。(摘要截短至250字)