首页> 外文期刊>Journal of neuroendocrinology >Investigating heterogeneity of intracellular calcium dynamics in anterior pituitary lactotrophs using a combined modelling/experimental approach.
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Investigating heterogeneity of intracellular calcium dynamics in anterior pituitary lactotrophs using a combined modelling/experimental approach.

机译:使用组合的建模/实验方法,研究垂体前叶营养型中细胞内钙动力学的异质性。

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摘要

Cell responses are commonly heterogeneous, even within a subpopulation. In the present study, we investigate the source of heterogeneity in the Ca(2+) response of anterior pituitary lactotrophs to a Ca(2+) mobilisation agonist, thyrotrophin-releasing hormone. This response is characterised by a sharp increase of cytosolic Ca(2+) concentration as a result of mobilisation of Ca(2+) from intracellular stores, followed by a decrease to an elevated plateau level that results from Ca(2+) influx. We focus on heterogeneity of the evoked Ca(2+) spike under extracellular Ca(2+) free conditions. We introduce a method that uses the information provided by a mathematical model to characterise the source of heterogeneity. This method compares scatter plots of features of the Ca(2+) response obtained experimentally with those made from the mathematical model. The model scatter plots reflect random variation of parameters over different ranges, and matching the experimental and model scatter plots allows us to predict which parameters are most variable. We find that a large degree of variation in Ca(2+) efflux is a likely key contributor to the heterogeneity of Ca(2+) responses to thyrotrophin-releasing hormone in lactotrophs. This technique is applicable to any situation in which the heterogeneous biological response is described by a mathematical model.
机译:细胞反应通常是异质的,即使在亚群中也是如此。在当前的研究中,我们调查了垂体前叶嗜茶菌对Ca(2+)动员激动剂,促甲状腺素释放激素的Ca(2+)反应的异质性来源。这种反应的特征是由于从细胞内存储中动员了Ca(2+),导致了细胞质Ca(2+)浓度的急剧增加,随后由于Ca(2+)涌入而导致了高原水平的降低。我们专注于细胞外Ca(2+)自由条件下诱发的Ca(2+)峰值的异质性。我们介绍一种使用数学模型提供的信息来表征异质性来源的方法。该方法比较了通过实验获得的Ca(2+)特征的散点图与从数学模型获得的散点图。模型散点图反映了参数在不同范围内的随机变化,匹配实验散点图和模型散点图可以让我们预测哪些参数变化最大。我们发现Ca(2+)外排的很大程度的变化可能是Ca(2+)对促营养素中促甲状腺素释放激素的Ca(2+)反应异质性的关键因素。该技术适用于通过数学模型描述异质生物反应的任何情况。

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