Fruman D A, Gamache D A, Ernest M J
Institute of Biological Sciences, Syntex Research, Palo Alto, CA 94303.
Agents Actions. 1991 Sep;34(1-2):16-9. doi: 10.1007/BF01993225.
Changes in the endogenous synthesis of inositol 1,4,5-trisphosphate (IP3) mass have been quantitated in human peripheral neutrophils stimulated with FMLP, LTB4 and PAF using a recently described, highly specific radioreceptor assay. Each agonist induced a concentration-dependent synthesis of IP3 which was detectable within 10 seconds after stimulation. IP3 production was short-lived, returning to basal levels within 90 seconds. The maximal stimulated level of IP3 in response to FMLP and LTB4 was 30-50 50 pmoles/10(7) neutrophils. PAF was more effective (approximately 100 pmoles IP3/10(7) neutrophils). The response to FMLP was inhibited by pertussis toxin, but was unaffected by cholera toxin. Pretreatment with cytochalasin B did not enhance IP3 synthesis. These findings are generally consistent with previous studies employing [3H]myo-inositol-prelabeled cells, and provide one of the first measurements of IP3 synthesis by mass in agonist-stimulated human neutrophils.
利用最近描述的一种高度特异性放射受体分析法,对用甲酰甲硫氨酰-亮氨酰-苯丙氨酸(FMLP)、白三烯B4(LTB4)和血小板活化因子(PAF)刺激的人外周血中性粒细胞中肌醇1,4,5-三磷酸(IP3)内源性合成量的变化进行了定量分析。每种激动剂均诱导IP3的浓度依赖性合成,在刺激后10秒内即可检测到。IP3的产生是短暂的,在90秒内恢复到基础水平。对FMLP和LTB4反应的IP3最大刺激水平为30 - 50皮摩尔/10⁷个中性粒细胞。PAF更有效(约100皮摩尔IP3/10⁷个中性粒细胞)。对FMLP的反应受百日咳毒素抑制,但不受霍乱毒素影响。用细胞松弛素B预处理并未增强IP3的合成。这些发现总体上与先前使用[³H]肌醇预标记细胞的研究一致,并首次提供了激动剂刺激的人中性粒细胞中IP3合成量的测量数据。