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1
Extracellular calcium concentration controls the frequency of intracellular calcium spiking independently of inositol 1,4,5-trisphosphate production in HeLa cells.细胞外钙浓度独立于HeLa细胞中肌醇1,4,5 - 三磷酸产生来控制细胞内钙闪烁的频率。
Biochem J. 1996 Feb 15;314 ( Pt 1)(Pt 1):347-54. doi: 10.1042/bj3140347.
2
The thiol reagent, thimerosal, evokes Ca2+ spikes in HeLa cells by sensitizing the inositol 1,4,5-trisphosphate receptor.硫醇试剂硫柳汞通过使肌醇1,4,5 -三磷酸受体敏感化,在HeLa细胞中引发钙离子峰。
J Biol Chem. 1992 Dec 15;267(35):25113-9.
3
All-or-nothing Ca2+ mobilization from the intracellular stores of single histamine-stimulated HeLa cells.单个组胺刺激的HeLa细胞胞内钙库中全或无的钙离子动员。
J Physiol. 1992 May;450:163-78. doi: 10.1113/jphysiol.1992.sp019121.
4
Glucose stimulates voltage- and calcium-dependent inositol trisphosphate production and intracellular calcium mobilization in insulin-secreting beta TC3 cells.葡萄糖刺激胰岛素分泌βTC3细胞中电压和钙依赖性三磷酸肌醇的产生以及细胞内钙动员。
Biochem J. 1996 Feb 15;314 ( Pt 1)(Pt 1):339-45. doi: 10.1042/bj3140339.
5
Control of calcium spiking frequency in pituitary gonadotrophs by a single-pool cytoplasmic oscillator.单池细胞质振荡器对垂体促性腺细胞中钙峰频率的控制
Mol Pharmacol. 1994 May;45(5):1013-21.
6
High calcium and other divalent cations increase inositol trisphosphate in bovine parathyroid cells.高钙及其他二价阳离子可增加牛甲状旁腺细胞中的肌醇三磷酸。
Endocrinology. 1988 Jul;123(1):382-9. doi: 10.1210/endo-123-1-382.
7
Fluoride stimulates the accumulation of inositol phosphates, increases intracellular free calcium, and inhibits parathyroid hormone release in dispersed bovine parathyroid cells.氟化物可刺激肌醇磷酸的积累,增加细胞内游离钙,并抑制分散的牛甲状旁腺细胞中甲状旁腺激素的释放。
Endocrinology. 1988 Jun;122(6):2833-9. doi: 10.1210/endo-122-6-2833.
8
Hepatocyte gap junctions are permeable to the second messenger, inositol 1,4,5-trisphosphate, and to calcium ions.肝细胞间隙连接可通透第二信使肌醇1,4,5-三磷酸以及钙离子。
Proc Natl Acad Sci U S A. 1989 Apr;86(8):2708-12. doi: 10.1073/pnas.86.8.2708.
9
Kinetics of cytosolic Ca2+ concentration after photolytic release of 1-D-myo-inositol 1,4-bisphosphate 5-phosphorothioate from a caged derivative in guinea pig hepatocytes.豚鼠肝细胞中笼形衍生物1-D-肌醇1,4-二磷酸5-硫代磷酸酯光解释放后胞质Ca2+浓度的动力学
Biophys J. 1995 Jun;68(6):2601-7. doi: 10.1016/S0006-3495(95)80444-3.
10
Reassessment of the Ca2+ sensing property of a type I metabotropic glutamate receptor by simultaneous measurement of inositol 1,4,5-trisphosphate and Ca2+ in single cells.通过在单细胞中同时测量肌醇1,4,5-三磷酸和Ca2+对I型代谢型谷氨酸受体Ca2+传感特性的重新评估
J Biol Chem. 2001 Jun 1;276(22):19286-93. doi: 10.1074/jbc.M007600200. Epub 2001 Feb 20.

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Fundamentals of Cellular Calcium Signaling: A Primer.细胞钙信号基础:入门篇。
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2
Photoswitchable diacylglycerols enable optical control of protein kinase C.可光开关的二酰基甘油实现对蛋白激酶C的光学控制。
Nat Chem Biol. 2016 Sep;12(9):755-62. doi: 10.1038/nchembio.2141. Epub 2016 Jul 25.
3
Differential Regulation of Multiple Steps in Inositol 1,4,5-Trisphosphate Signaling by Protein Kinase C Shapes Hormone-stimulated Ca2+ Oscillations.蛋白激酶C对肌醇1,4,5-三磷酸信号传导多个步骤的差异调节塑造了激素刺激的钙离子振荡。
J Biol Chem. 2015 Jul 24;290(30):18519-33. doi: 10.1074/jbc.M115.657767. Epub 2015 Jun 15.
4
Regulation of oscillation dynamics in biochemical systems with dual negative feedback loops.双负反馈环生物化学系统中的振动态调控。
J R Soc Interface. 2012 Aug 7;9(73):1998-2010. doi: 10.1098/rsif.2012.0028. Epub 2012 Mar 14.
5
Orai3--the 'exceptional' Orai?Orai3--那个“例外”的 Orai?
J Physiol. 2012 Jan 15;590(2):241-57. doi: 10.1113/jphysiol.2011.220574. Epub 2011 Oct 31.
6
Orai channel-dependent activation of phospholipase C-δ: a novel mechanism for the effects of calcium entry on calcium oscillations.钙通道依赖性激活磷酯酶 C-δ:钙内流对钙震荡影响的新机制。
J Physiol. 2011 Nov 1;589(Pt 21):5057-69. doi: 10.1113/jphysiol.2011.214437. Epub 2011 Aug 30.
7
Calpain-1 cleaves Rad21 to promote sister chromatid separation.钙蛋白酶-1将 Rad21 裂解以促进姐妹染色单体分离。
Mol Cell Biol. 2011 Nov;31(21):4335-47. doi: 10.1128/MCB.06075-11. Epub 2011 Aug 29.
8
Arachidonic acid, ARC channels, and Orai proteins.花生四烯酸、ARC通道和Orai蛋白。
Cell Calcium. 2009 Jun;45(6):602-10. doi: 10.1016/j.ceca.2009.02.001. Epub 2009 Mar 17.
9
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Hepatology. 2008 Oct;48(4):1273-81. doi: 10.1002/hep.22461.
10
Modulation of Ca(2+) release and Ca(2+) oscillations in HeLa cells and fibroblasts by mitochondrial Ca(2+) uniporter stimulation.通过线粒体钙单向转运体刺激调节HeLa细胞和成纤维细胞中的钙释放和钙振荡。
J Physiol. 2007 Apr 1;580(Pt 1):39-49. doi: 10.1113/jphysiol.2006.126391. Epub 2007 Jan 18.

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Acceleration of intracellular calcium waves in Xenopus oocytes by calcium influx.钙内流对非洲爪蟾卵母细胞内钙波的加速作用。
Science. 1993 Apr 9;260(5105):229-32. doi: 10.1126/science.8385801.
2
Ca2+ oscillations in non-excitable cells.非兴奋性细胞中的钙离子振荡
Annu Rev Physiol. 1993;55:427-54. doi: 10.1146/annurev.ph.55.030193.002235.
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Inositol trisphosphate and calcium signalling.肌醇三磷酸与钙信号传导
Nature. 1993 Jan 28;361(6410):315-25. doi: 10.1038/361315a0.
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Model for receptor-controlled cytosolic calcium oscillations and for external influences on the signal pathway.受体控制的胞质钙振荡模型以及信号通路的外部影响模型。
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A single-pool model for intracellular calcium oscillations and waves in the Xenopus laevis oocyte.非洲爪蟾卵母细胞中细胞内钙振荡和波的单池模型。
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Modulation of signalling initiated by phosphoinositidase-C-linked receptors.
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Critical intracellular Ca2+ concentration for all-or-none Ca2+ spiking in single smooth muscle cells.单个平滑肌细胞中全或无Ca2+ 尖峰的临界细胞内Ca2+ 浓度。
EMBO J. 1993 Dec 15;12(13):5287-91. doi: 10.1002/j.1460-2075.1993.tb06224.x.
8
Muscarinic receptor-mediated inositol 1,4,5-trisphosphate formation in SH-SY5Y neuroblastoma cells is regulated acutely by cytosolic Ca2+ and by rapid desensitization.毒蕈碱受体介导的SH-SY5Y神经母细胞瘤细胞中肌醇1,4,5-三磷酸的形成受胞质Ca2+和快速脱敏的急性调节。
J Neurochem. 1994 Jul;63(1):177-85. doi: 10.1046/j.1471-4159.1994.63010177.x.
9
Control of calcium spiking frequency in pituitary gonadotrophs by a single-pool cytoplasmic oscillator.单池细胞质振荡器对垂体促性腺细胞中钙峰频率的控制
Mol Pharmacol. 1994 May;45(5):1013-21.
10
Cytoplasmic Ca2+ determines the rate of Ca2+ entry into Mardin-Darby canine kidney-focus (MDCK-F) cells.细胞质中的钙离子决定了钙离子进入马尔汀-达比犬肾聚焦细胞(MDCK-F细胞)的速率。
Pflugers Arch. 1994 Jan;426(1-2):95-100. doi: 10.1007/BF00374676.

细胞外钙浓度独立于HeLa细胞中肌醇1,4,5 - 三磷酸产生来控制细胞内钙闪烁的频率。

Extracellular calcium concentration controls the frequency of intracellular calcium spiking independently of inositol 1,4,5-trisphosphate production in HeLa cells.

作者信息

Bootman M D, Young K W, Young J M, Moreton R B, Berridge M J

机构信息

The Babraham Institute Laboratory of Molecular Signalling, Department of Zoology, University of Cambridge, U.K.

出版信息

Biochem J. 1996 Feb 15;314 ( Pt 1)(Pt 1):347-54. doi: 10.1042/bj3140347.

DOI:10.1042/bj3140347
PMID:8660306
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1217048/
Abstract

Stimulation of single HeLa cells with histamine evoked repetitive increases of the intracellular calcium ion concentration (Ca2+ spikes). The frequency of Ca2+ spiking increased as the extracellular hormone concentration was elevated. In addition, the frequency of Ca2+ spiking could be accelerated by increasing the extracellular Ca2+ concentration ([Ca2+]0) in the presence of a constant hormone concentration. The range of [Ca2+]0 over which the spiking frequency could be titrated was nominally-zero to 10mM, being half-maximally effective at approx. 1 and 2.5mM for 37 and 22 degrees C respectively. The effect of [Ca2+]0 on inositol phosphates production was also examined. Changes of [Ca2+]0 over a range which had been found to affect the frequency of Ca2+ spiking did not have any effect on the rate of myo-inositol 1,4,5-trisphosphate (InsP3) production, although an increase in inositol phosphates production was observed as [Ca2+]0 was increased from zero to values giving less than half-maximal Ca2+ spike frequency. These data suggest that at low Ca2+ spike frequency, Ca2+-stimulated activation of phospholipase C may contribute to Ca2+ spiking in HeLa cells, but under some conditions the availability of Ca2+ to the intracellular stores, rather than changes in the rate of InsP3 production, determines the Ca2+ spike frequency.

摘要

用组胺刺激单个海拉细胞会引起细胞内钙离子浓度的反复增加(钙离子尖峰)。随着细胞外激素浓度升高,钙离子尖峰的频率增加。此外,在激素浓度恒定的情况下,通过增加细胞外钙离子浓度([Ca2+]0)可加速钙离子尖峰的频率。能够对尖峰频率进行滴定的[Ca2+]0范围名义上为零至10mM,在37℃和22℃时分别约为1mM和2.5mM时达到最大效应的一半。还研究了[Ca2+]0对肌醇磷酸生成的影响。在已发现会影响钙离子尖峰频率的范围内改变[Ca2+]0,对肌醇-1,4,5-三磷酸(InsP3)的生成速率没有任何影响,尽管当[Ca2+]0从零增加到产生小于最大钙离子尖峰频率一半的值时,观察到肌醇磷酸生成增加。这些数据表明,在低钙离子尖峰频率下,钙离子刺激的磷脂酶C活化可能有助于海拉细胞中的钙离子尖峰,但在某些情况下,细胞内储存库可利用的钙离子而非InsP3生成速率的变化决定了钙离子尖峰频率。