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在二甲基亚砜存在的情况下将水母发光蛋白快速加载到血小板中——对各种激动剂的反应(透光率和钙的变化)特征。

Rapid aequorin loading into platelets in the presence of DMSO--characteristics of the responses (changes in light transmission and in calcium) to various agonists.

作者信息

Potevin F, Lecompte T, Favier R, Samama M

机构信息

Central Laboratory of Hematology, Hôtel-Dieu Hospital, Paris, France.

出版信息

Thromb Haemost. 1991 Sep 2;66(3):334-42.

PMID:1746005
Abstract

We have looked at different parameters which could modify platelet behaviour during and after aequorin loading in the presence of DMSO. There is a decreased platelet reactivity in response to ADP, PAF and A-23,187 which appears to be mainly due to the exposure to EGTA during washing and loading and the 1 ml volume of the test suspension. All the studied agonists (including PMA) which elicit aggregation are able to induce an intracellular Ca2+ change detected with the aequorin probe. By contrast, epinephrine alone induces neither aggregation nor Ca2+ rise, but potentiates the responses to ADP. Different consecutive phases in Ca2+ changes after stimulation with ADP, PMA and A-23,187 can be evidenced. In the presence of external Ca2+, the second component of the Ca2+ change evoked with ADP is dependent on aggregation and the subsequent TXA2 synthesis. When the external medium is Ca2+ depleted, the two Ca2+ peaks induced by ADP disappear whereas a Ca2+ rise persists (endogenous mobilization) with the other agonists, being independent of TXA2 and ADP release. Ca2+ mobilization parallels activation with A-23,187 but not with low concentrations of thrombin.

摘要

我们研究了不同参数,这些参数可能会在二甲基亚砜(DMSO)存在的情况下,改变水母发光蛋白加载期间及之后血小板的行为。在响应二磷酸腺苷(ADP)、血小板活化因子(PAF)和A-23,187时,血小板反应性降低,这似乎主要是由于洗涤和加载过程中暴露于乙二醇双四乙酸(EGTA)以及测试悬浮液1毫升的体积所致。所有研究的能引发聚集的激动剂(包括佛波酯(PMA))都能够诱导用水母发光蛋白探针检测到的细胞内钙离子(Ca2+)变化。相比之下,单独的肾上腺素既不诱导聚集也不引起Ca2+升高,但会增强对ADP的反应。在用ADP、PMA和A-23,187刺激后,Ca2+变化的不同连续阶段可以得到证实。在存在细胞外Ca2+的情况下,由ADP引发的Ca2+变化的第二个成分取决于聚集以及随后的血栓素A2(TXA2)合成。当细胞外培养基中Ca2+耗尽时,由ADP诱导的两个Ca2+峰消失,而其他激动剂则持续存在Ca2+升高(内源性动员),且与TXA2和ADP释放无关。Ca2+动员与A-23,187的激活平行,但与低浓度凝血酶的激活不平行。

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