Savic V, Blanchard A, Vlahovic P, Stefanovic V, Ardaillou N, Ardaillou R
INSERM 64, Hôpital Tenon, Paris, France.
Arch Biochem Biophys. 1991 Oct;290(1):202-6. doi: 10.1016/0003-9861(91)90609-m.
The ecto-5'-nucleotidase activity of rat glomerular mesangial cells increases after exposure to prostaglandin E2 (PGE2) via cAMP stimulation (Savic et al., 1990, Immunology 70, 321). Therefore we examined whether other cAMP-stimulating agents had a similar effect. Forskolin (1 microM), PGE2 (10 microM), and isoproterenol (10 microM), three products stimulating rat mesangial cell adenylate cyclase activity, enhanced cAMP accumulation within 5 min and 5'-nucleotidase activity after a lag time of at least 24 h, 3-Isobutyl-1-methylxanthine (IBMX) and Ro 20-1724, two drugs inhibiting cAMP degradation, also stimulated cAMP accumulation and 5'-nucleotidase activity. The effects of these agents on 5'-nucleotidase activity were additive with those of the three products stimulating adenylate cyclase activity, except for Ro 20-1724 and forskolin which acted synergistically. Cycloheximide, a blocker of protein synthesis, suppressed the cAMP-dependent increase of 5'-nucleotidase activity. Because ecto-5'-nucleotidase activity is a marker of cell differentiation, the effect of the same cAMP-stimulating agents on cell proliferation was also studied. Forskolin, PGE2, and isoproterenol inhibited [3H]thymidine incorporation into rat mesangial cells in a dose-dependent manner. The same effect was obtained with IBMX (100 microM) and Ro 20-1724 (50 microM). Stimulation of 5'-nucleotidase activity and inhibition of [3H]thymidine incorporation occurred over the same range of concentrations for the various agonists tested. Taken together, these results indicate that expression of ecto-5'-nucleotidase in rat mesangial cells is induced by cAMP whatever the reason for its accumulation. The simultaneous inhibition of DNA synthesis may occur independently or be associated with the stimulation of 5'-nucleotidase expression.
大鼠肾小球系膜细胞的胞外5'-核苷酸酶活性在通过环磷酸腺苷(cAMP)刺激暴露于前列腺素E2(PGE2)后会增加(萨维奇等人,1990年,《免疫学》70卷,321页)。因此,我们研究了其他cAMP刺激剂是否有类似作用。福斯高林(1微摩尔)、PGE2(10微摩尔)和异丙肾上腺素(10微摩尔)这三种刺激大鼠系膜细胞腺苷酸环化酶活性的物质,在5分钟内增强了cAMP的积累,并在至少24小时的延迟时间后增强了5'-核苷酸酶活性。3-异丁基-1-甲基黄嘌呤(IBMX)和Ro 20-1724这两种抑制cAMP降解的药物,也刺激了cAMP的积累和5'-核苷酸酶活性。这些物质对5'-核苷酸酶活性的影响与三种刺激腺苷酸环化酶活性的物质的影响是相加的,但Ro 20-1724和福斯高林起协同作用。蛋白质合成阻滞剂环己酰亚胺抑制了5'-核苷酸酶活性的cAMP依赖性增加。由于胞外5'-核苷酸酶活性是细胞分化的一个标志物,还研究了相同的cAMP刺激剂对细胞增殖的影响。福斯高林、PGE2和异丙肾上腺素以剂量依赖性方式抑制[3H]胸腺嘧啶核苷掺入大鼠系膜细胞。用IBMX(100微摩尔)和Ro 20-1724(50微摩尔)也得到了相同的效果。对于所测试的各种激动剂,5'-核苷酸酶活性的刺激和[3H]胸腺嘧啶核苷掺入的抑制发生在相同的浓度范围内。综上所述,这些结果表明大鼠系膜细胞中胞外5'-核苷酸酶的表达是由cAMP诱导的,无论其积累的原因是什么。DNA合成的同时抑制可能独立发生,也可能与5'-核苷酸酶表达的刺激相关。