Ricupero D, Taylor L, Polgar P
Boston University School of Medicine, MA 02118.
Agents Actions. 1993 Sep;40(1-2):110-8. doi: 10.1007/BF01976759.
Rise in free cytosolic calcium concentrations [Ca2+]i in response to bradykinin and guanosine 5'-O-thiotriphosphate (GTP tau S) was related to the action of phospholipase A/ (arachidonic acid release). At 900 microM extracellular CaCl2, bradykinin induced a typical Ca2+ movement consisting of an initial [Ca2+]i peak at approximately 400 nM followed by a sustained increase in the steady-state cytosolic Ca2+ level at approximately 290 nM. As the extracellular CaCl2 concentration was reduced to 100 microM, the bradykinin induced initial spike was reduced followed by only a marginal increase in steady-state cytosolic Ca2+ levels. Treatment of endothelial cells with saponin (0.002% w/w) did not increase [Ca2+]i and saponin treated cells exhibited a very similar pattern of Ca2+ mobilization in response to bradykinin. However, with saponin treatment, GTP tau S (100 microM) increased [Ca2+]i at an almost identical tracing exhibited with 50 nM bradykinin stimulation (in either the presence or absence of 0.002% saponin). No additive increase in [Ca2+]i was observed in cells stimulated with both 100 microM GTP tau S and 50 nM bradykinin or in bradykinin stimulated cells subsequently exposed to GTP tau S. Pertussis toxin (PTX) did not affect the bradykinin induced Ca2+ mobilization. However, as we showed previously, PTX inhibited bradykinin stimulated arachidonic acid release. These results indicate transduction of the bradykinin signal by G-protein for both phospholipase A2 (PLA2) activation and Ca2+ mobilization but likely by different G alpha subunits, a PTX sensitive and an insensitive subunit. Furthermore, the bradykinin and GTP tau S stimulated release of arachidonic acid appears to be only partially dependent on [Ca2+]i.(ABSTRACT TRUNCATED AT 250 WORDS)
缓激肽和5'-O-硫代三磷酸鸟苷(GTPτS)引起的游离胞质钙浓度[Ca2+]i升高与磷脂酶A/(花生四烯酸释放)的作用有关。在900微摩尔/升细胞外氯化钙存在时,缓激肽诱导典型的钙移动,包括最初约400纳摩尔的[Ca2+]i峰值,随后稳态胞质钙水平持续升高至约290纳摩尔。随着细胞外氯化钙浓度降至100微摩尔/升,缓激肽诱导的初始峰值降低,随后稳态胞质钙水平仅略有升高。用皂苷(0.002%w/w)处理内皮细胞不会增加[Ca2+]i,且经皂苷处理的细胞对缓激肽的钙动员模式非常相似。然而,经皂苷处理后,GTPτS(100微摩尔/升)使[Ca2+]i升高,其追踪曲线与50纳摩尔缓激肽刺激时几乎相同(无论有无0.002%皂苷)。在用100微摩尔/升GTPτS和50纳摩尔缓激肽刺激的细胞中,或在缓激肽刺激后再暴露于GTPτS的细胞中,均未观察到[Ca2+]i的叠加升高。百日咳毒素(PTX)不影响缓激肽诱导的钙动员。然而,如我们之前所示,PTX抑制缓激肽刺激的花生四烯酸释放。这些结果表明,G蛋白转导缓激肽信号以激活磷脂酶A2(PLA2)和动员钙,但可能通过不同的Gα亚基,一个对PTX敏感,一个对PTX不敏感。此外,缓激肽和GTPτS刺激的花生四烯酸释放似乎仅部分依赖于[Ca2+]i。(摘要截短于250字)