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血小板活化因子调节盘基网柄菌中的信号转导。

Platelet activating factor modulates signal transduction in Dictyostelium.

作者信息

Sordano C, Cristino E, Bussolino F, Wurster B, Bozzaro S

机构信息

Department of Clinical and Biological Sciences, University of Turin, Ospedale S. Luigi, Orbassano-Torino, Italy.

出版信息

J Cell Sci. 1993 Jan;104 ( Pt 1):197-202. doi: 10.1242/jcs.104.1.197.

DOI:10.1242/jcs.104.1.197
PMID:8383695
Abstract

During development, Dictyostelium discoideum cells produce platelet activating factor (PAF). When cells are stimulated with external cAMP pulses, PAF is transiently synthesized. To determine whether PAF is involved in signal transduction, we have tested the effect of PAF on some cellular responses which are regulated by cAMP, such as spontaneous light-scattering oscillations of suspended cells, cAMP relay, transient increases of cGMP level, and extracellular calcium uptake. Our results show that PAF specifically interferes with spontaneous spike-shaped oscillations, without affecting sinusoidal ones. PAF increases the amplitude of a spike, but has no effects on its phase or frequency. When cells fail to oscillate spontaneously, PAF does not induce spikes; however, if administered together with cAMP, it amplifies the light-scattering response to cAMP. Amplification of light-scattering changes is accompanied by a threefold increase in the concentration levels of both cellular cAMP and cGMP. Extracellular Ca2+ uptake is also stimulated by PAF. This latter response is independent of endogenous or exogenously added cAMP. All these effects are specific for the naturally occurring R-enantiomer of PAF, the S-enantiomer and lyso-PAF being inactive. These results suggest that PAF modulates signal transduction in Dictyostelium, probably by interacting with an intracellular acceptor, which is involved in the pathways regulating membrane Ca2+ channels, adenylate and guanylate cyclase.

摘要

在发育过程中,盘基网柄菌细胞会产生血小板活化因子(PAF)。当细胞受到外部环磷酸腺苷(cAMP)脉冲刺激时,PAF会被短暂合成。为了确定PAF是否参与信号转导,我们测试了PAF对一些受cAMP调节的细胞反应的影响,如悬浮细胞的自发光散射振荡、cAMP信号传递、cGMP水平的短暂升高以及细胞外钙摄取。我们的结果表明,PAF特异性地干扰自发的尖峰状振荡,而不影响正弦振荡。PAF增加了尖峰的幅度,但对其相位或频率没有影响。当细胞不能自发振荡时,PAF不会诱导尖峰;然而,如果与cAMP一起施用,它会放大对cAMP的光散射反应。光散射变化的放大伴随着细胞内cAMP和cGMP浓度水平增加三倍。PAF也刺激细胞外Ca2+摄取。后一种反应独立于内源性或外源性添加的cAMP。所有这些效应对于天然存在的PAF的R-对映体是特异性的,S-对映体和溶血PAF无活性。这些结果表明,PAF可能通过与细胞内受体相互作用来调节盘基网柄菌中的信号转导,该受体参与调节膜Ca2+通道、腺苷酸环化酶和鸟苷酸环化酶的信号通路。

相似文献

1
Platelet activating factor modulates signal transduction in Dictyostelium.血小板活化因子调节盘基网柄菌中的信号转导。
J Cell Sci. 1993 Jan;104 ( Pt 1):197-202. doi: 10.1242/jcs.104.1.197.
2
Stimulation of calcium influx by platelet activating factor in Dictyostelium.血小板激活因子对盘基网柄菌中钙内流的刺激作用。
J Cell Sci. 1995 Apr;108 ( Pt 4):1597-603. doi: 10.1242/jcs.108.4.1597.
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Oscillations of Ca++ concentration during the cell differentiation of Dictyostelium discoideum: their relation to oscillations in cyclic AMP and other components.盘基网柄菌细胞分化过程中钙离子浓度的振荡:其与环磷酸腺苷及其他成分振荡的关系
Differentiation. 1986;31(2):85-91. doi: 10.1111/j.1432-0436.1986.tb00387.x.
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cGMP potentiates receptor-stimulated Ca2+ influx in Dictyostelium discoideum.环磷酸鸟苷(cGMP)增强盘基网柄菌中受体刺激的钙离子内流。
Biochim Biophys Acta. 1998 Mar 12;1402(1):102-8. doi: 10.1016/s0167-4889(97)00142-0.
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Dictyostelium cells produce platelet-activating factor in response to cAMP.盘基网柄菌细胞在响应环磷酸腺苷(cAMP)时会产生血小板活化因子。
Eur J Biochem. 1991 Mar 28;196(3):609-15. doi: 10.1111/j.1432-1033.1991.tb15856.x.
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Platelet-activating factor stimulates multiple signaling pathways in cultured rat mesangial cells.血小板活化因子刺激培养的大鼠系膜细胞中的多种信号通路。
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Cellular responsiveness to cyclic AMP in a phosphodiesterase-defective mutant of Dictyostelium discoideum.盘基网柄菌磷酸二酯酶缺陷型突变体中细胞对环磷酸腺苷的反应性
Cell Differ. 1982 May;11(3):117-23. doi: 10.1016/0045-6039(82)90001-x.
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A model for cAMP-mediated cGMP response in Dictyostelium discoideum.盘基网柄菌中cAMP介导的cGMP反应模型。
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cGMP-phosphodiesterase antagonists inhibit Ca2+-influx in Dictyostelium discoideum and bovine cyclic-nucleotide-gated-channel.环磷酸鸟苷磷酸二酯酶拮抗剂可抑制盘基网柄菌和牛环核苷酸门控通道中的钙离子内流。
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Oscillations of cyclic nucleotide concentrations in relation to the excitability of Dictyostelium cells.
J Exp Biol. 1979 Aug;81:33-47. doi: 10.1242/jeb.81.1.33.

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