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钙离子载体A23187通过将佛波酯受体从低亲和力状态转变为高亲和力状态,增强了由佛波二丁酸酯刺激的人类中性粒细胞超氧化物释放。

Calcium ionophore A23187 enhances human neutrophil superoxide release, stimulated by phorbol dibutyrate, by converting phorbol ester receptors from a low- to high-affinity state.

作者信息

French J K, Hurst N P, Zalewski P D, Valente L, Forbes I J

出版信息

FEBS Lett. 1987 Feb 23;212(2):242-6. doi: 10.1016/0014-5793(87)81353-4.

Abstract

The calcium ionophore A23187 acted synergistically with phorbol dibutyrate (PDBu) to stimulate human neutrophil superoxide production. A23187 shortened the lag period and markedly increased the initial rate of neutrophil superoxide production induced by suboptimal concentrations of PDBu. 1 microM A23187 reduced the EC50 value for superoxide release from 56 to 8 nM PDBu. This effect of A23187 was correlated with enhanced binding of [3H]PDBu to its receptor and a reduction in the dissociation constant (Kd) from 27 to 10 nM, without altering the apparent total number of phorbol dibutyrate receptors. These actions of A23187 were abolished in the presence of EGTA or TMB-8, confirming a dependence on Ca2+.

摘要

钙离子载体A23187与佛波醇二丁酸酯(PDBu)协同作用,刺激人中性粒细胞产生超氧化物。A23187缩短了延迟期,并显著提高了次优浓度PDBu诱导的中性粒细胞超氧化物产生的初始速率。1微摩尔A23187将超氧化物释放的EC50值从56纳摩尔降至8纳摩尔PDBu。A23187的这种作用与[3H]PDBu与其受体的结合增强以及解离常数(Kd)从27纳摩尔降至10纳摩尔相关,而不改变佛波醇二丁酸酯受体的表观总数。在EGTA或TMB-8存在的情况下,A23187的这些作用被消除,证实了对Ca2+的依赖性。

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