首页> 外文期刊>The Journal of Physiology >Ca2+ store dynamics determines the pattern of activation of the store-operated Ca2+ current I(CRAC) in response to InsP3 in rat basophilic leukaemia cells.
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Ca2+ store dynamics determines the pattern of activation of the store-operated Ca2+ current I(CRAC) in response to InsP3 in rat basophilic leukaemia cells.

机译:Ca2 +存储动力学决定了大鼠嗜碱性白血病细胞中响应InsP3的存储操作的Ca2 +电流I(CRAC)的激活模式。

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摘要

1. The relationship between the amplitude of the store-operated Ca2+ ICR AC and intracellular inositol 1,4,5-triphosphate (InsP3) concentration is complex. In rat basophilic leukaemia (RBL-1) cells dialysed with high intracellular Ca2+ buffer, the relationship is supra-linear with a Hill coefficient of 12 and resembles an apparent 'all-or-none' phenomenon. The non-linearity seems to arise from InsP3 metabolism. However, it is not clear which InsP3-metabolising pathway engenders the non-linear behaviour nor whether ICRAC is always activated to its maximal extent by InsP3. 2. Using the whole-cell patch clamp technique, we dialysed RBL-1 cells with different concentrations of the InsP3 analogue InsP3-F. InsP3-F is broken down by Ins(1,4,5)P3 5-phosphatase but is not a substrate for Ins(1,4,5)P3 3-kinase. The relationship between InsP3-F and ICRAC amplitude was supra-linear and very similar to that with InsP3 but was distinct from the graded relationship seen with the non-metabolisable analogue Ins2,4,5P3. 3. In the presence of high intracellular Ca2+ buffer, InsP3-F activated ICRAC to its maximal extent. With moderate Ca2+ buffer, however, sub-maximal ICRAC could be obtained to a maximal InsP3-F concentration. Nevertheless, the relationship between the amplitude of ICRAC and InsP3-F concentration was still supra-linear. 4. Submaximal ICRAC in response to InsP3-F in the presence of moderate Ca2+ buffer was due to partial depletion of the stores, because the size of the current could be increased by thapsigargin. 5. The data suggest that first Ins(1,4,5)P3 5-phosphatase is an important factor which contributes to the non-linear relationship between InsP3 concentration and the amplitude of ICRAC and second, InsP3 does not always activate ICRAC to its maximal extent. At moderate buffer strengths, submaximal ICRAC is evoked by maximal InsP3. However, the supra-linear relationship between InsP3 concentration and amplitude of the current still holds.
机译:1.储存操作的Ca2 + ICR AC的振幅与细胞内肌醇1,4,5-三磷酸(InsP3)浓度之间的关系很复杂。在用高细胞内Ca2 +缓冲液透析的大鼠嗜碱性白血病(RBL-1)细胞中,这种关系是超线性的,希尔系数为12,类似于明显的“全有或全无”现象。非线性似乎是由InsP3代谢引起的。但是,尚不清楚哪个InsP3代谢途径引起非线性行为,也不清楚ICRAC是否始终被InsP3激活到最大程度。 2.使用全细胞膜片钳技术,用不同浓度的InsP3类似物InsP3-F透析RBL-1细胞。 InsP3-F被Ins(1,4,5)P3 5-磷酸酶分解,但不是Ins(1,4,5)P3 3-激酶的底物。 InsP3-F和ICRAC振幅之间的关系是超线性的,与InsP3的关系非常相似,但与不可代谢的类似物Ins2,4,5P3的梯度关系不同。 3.在高细胞内Ca2 +缓冲液存在下,InsP3-F最大限度地激活了ICRAC。然而,使用适度的Ca2 +缓冲液,可以获得最大InsP3-F浓度的次最大ICRAC。尽管如此,ICRAC的振幅和InsP3-F浓度之间的关系仍然是超线性的。 4.在中等Ca2 +缓冲液存在下对InsP3-F响应的最大ICRAC归因于部分存储库耗尽,因为thapsigargin可以增加电流大小。 5.数据表明,第一个Ins(1,4,5)P3 5-磷酸酶是导致InsP3浓度与ICRAC振幅之间非线性关系的重要因素,其次,InsP3并不总是将ICRAC激活至其最大程度。在中等缓冲强度下,最大InsP3会引起次最大ICRAC。但是,InsP3浓度与电流幅度之间的超线性关系仍然成立。

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