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通过时间分辨光子计数荧光法进行细胞内钙测量的发展。

Development of intracellular calcium measurement by time-resolved photon-counting fluorescence.

作者信息

Schoutteten L, Denjean P, Joliff-Botrel G, Bernard C, Pansu D, Pansu R B

机构信息

Ecole Normale Supérieure de Cachan, France.

出版信息

Photochem Photobiol. 1999 Nov;70(5):701-9.

Abstract

Calcium green I, a ratiometric probe based on fluorescence lifetime measurements, was used to monitor intracellular calcium activity ([Ca2+]i) in RINm5F cells using a time-resolved fluorescence confocal microscope. The probe affinity constant has been recalibrated in single cells using ionomycin as a calcium ionophore and ethylenebis(oxyethylenenitrilo)tetraacetic acid as a calcium buffer; Kd was found to equal 150 nmol/L. The kinetics of ionomycin equilibration showed that the calcium release from calcium stores occurs before equilibration with extracellular calcium. The response to the muscarinic agonist carbachol, measured on 17 cells receiving three consecutive applications was characterized both by a [Ca2+]i peak lasting 50 s without any trailing plateau and by desensitization with a 30% decrease in the response. The dose-dependent response was obtained for a carbachol concentration from 5 mumol/L to 0.5 mmol/L. The ability of our set-up to obtain a value every 10 ms enabled us to record asynchronous spikes of [Ca2+]i in the RINm5F cells. The spikes, lasting less than 1 s, are significantly bigger than the noise, and they are not observed in the colonic HT29 cells.

摘要

钙绿 I 是一种基于荧光寿命测量的比率型探针,利用时间分辨荧光共聚焦显微镜来监测 RINm5F 细胞内的钙活性([Ca2+]i)。使用离子霉素作为钙离子载体,乙二胺四乙酸二钠作为钙缓冲剂,在单细胞中重新校准了探针亲和常数;发现解离常数(Kd)等于 150 nmol/L。离子霉素平衡动力学表明,钙从钙库释放发生在与细胞外钙平衡之前。对 17 个连续接受三次应用的细胞测量毒蕈碱激动剂卡巴胆碱的反应,其特征是[Ca2+]i 峰值持续 50 秒且无任何拖尾平台,以及脱敏反应,反应降低了 30%。对于卡巴胆碱浓度从 5 μmol/L 到 0.5 mmol/L,获得了剂量依赖性反应。我们的装置每 10 毫秒获取一个值的能力使我们能够记录 RINm5F 细胞中[Ca2+]i 的异步尖峰。这些尖峰持续时间不到 1 秒,明显大于噪声,在结肠 HT29 细胞中未观察到。

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