Mollace V, Colasanti M, Rodino P, Lauro G M, Nistico G
Department of Biology, University of Rome Tor Vergata, Italy.
Biochem Biophys Res Commun. 1994 Aug 30;203(1):87-92. doi: 10.1006/bbrc.1994.2152.
The role of the L-arginine-NO pathway on the formation of PGE2 by cultured astroglial cells incubated with the HIV coating glycoprotein gp120 was investigated. Preincubation of human cultured T 67 astrocytoma cells with gp 120 (100-500 nM) produced a significant increase of nitrite (the breakdown product of NO) and PGE2 in cell supernatants. The effect of gp 120 on both nitrite and PGE2 production was antagonized by inhibition of NO synthase by L-NAME (20-300 microM). The inhibition of gp120-induced PGE2 production by L-NAME was reverted by addition of arachidonic acid (30 microM), an effect antagonized by the cyclo-oxygenase inhibitor indomethacin (10 microM). Methylen bleu, an inhibitor of the biological activity of NO acting at the guanylate cyclase level failed to affect gp 120-mediated PGE2 release showing that the increase of cGMP subsequent to NO production was not involved in the modulatory activity of NO on arachidonic acid cascade. On the basis of present experiments we conclude that gp-120-induced release of PGE2 by astroglial cells is driven by NO, thereby contributing in the involvement of glial cells in HIV-related cerebral disorders.
研究了L-精氨酸-一氧化氮(NO)途径在与HIV包膜糖蛋白gp120孵育的培养星形胶质细胞形成前列腺素E2(PGE2)过程中的作用。用gp120(100 - 500 nM)预孵育人培养的T 67星形细胞瘤细胞,可使细胞上清液中的亚硝酸盐(NO的分解产物)和PGE2显著增加。L- NAME(20 - 300 microM)抑制一氧化氮合酶可拮抗gp120对亚硝酸盐和PGE2产生的影响。添加花生四烯酸(30 microM)可逆转L- NAME对gp120诱导的PGE2产生的抑制作用,而环氧化酶抑制剂吲哚美辛(10 microM)可拮抗该作用。亚甲蓝是一种作用于鸟苷酸环化酶水平的NO生物活性抑制剂,未能影响gp120介导的PGE2释放,表明NO产生后cGMP的增加不参与NO对花生四烯酸级联反应的调节活性。基于目前的实验,我们得出结论,gp - 120诱导星形胶质细胞释放PGE2是由NO驱动的,从而导致胶质细胞参与与HIV相关的脑部疾病。