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巨核细胞分泌反应的特征:内源性ATP持续监测释放的研究

Characterization of the megakaryocyte secretory response: studies of continuously monitored release of endogenous ATP.

作者信息

Miller J L

出版信息

Blood. 1983 May;61(5):967-72.

PMID:6403084
Abstract

Megakaryocytes share a number of structural and chemical properties with their progeny, blood platelets. With the availability of highly purified preparations of megakaryocytes isolated from guinea pig bone marrow, it is now also possible to study functional aspects of these cells. The present work reports the first study of the release of endogenously stored materials in megakaryocytes. Guinea pig megakaryocytes isolated to 75%-90% purity were exposed to thrombin or calcium ionophore (A23187) and the release of ATP was continuously monitored with the luciferin-luciferase reaction. Both maximal extent and initial rate of release were studied. Thrombin-induced release was half-maximal at thrombin concentrations of 0.2-0.5 NIH U/ml. At 4 U/ml thrombin, maximal release was 538 +/- 147 nmole ATP/10(9) megakaryocytes. A23187 induced half-maximal responses at concentrations of 7-8 microM. ATP release by ionophore showed a nearly absolute requirement for extracellular calcium, with release by thrombin showing only a partial calcium dependence. Following overnight culture, the response to thrombin was unchanged, whereas ATP release in response to ionophore was consistently increased (p less than 0.01). By comparison of maximally releasable ATP with total cellular ATP content, the storage pool of ATP in megakaryocytes was determined to comprise only 2%-6% of total megakaryocyte ATP, in contrast to an ATP storage pool of 20%-30% in guinea pig platelets. This difference may reflect further entry of ATP into the storage pool compartment or an enhanced ability of the cell to recognize and respond fully to platelet stimuli as the megakaryocyte reaches full maturity.

摘要

巨核细胞与其子代血小板具有许多结构和化学特性。随着从豚鼠骨髓中分离出高度纯化的巨核细胞制剂,现在也能够研究这些细胞的功能方面。本研究报告了对巨核细胞内源性储存物质释放的首次研究。将纯度达到75%-90%的豚鼠巨核细胞暴露于凝血酶或钙离子载体(A23187),并通过荧光素-荧光素酶反应持续监测ATP的释放。研究了释放的最大程度和初始速率。凝血酶诱导的释放在凝血酶浓度为0.2-0.5 NIH U/ml时达到最大释放量的一半。在4 U/ml凝血酶作用下,最大释放量为538±147 nmol ATP/10⁹个巨核细胞。A23187在浓度为7-8 μM时诱导出最大释放量的一半。离子载体诱导的ATP释放几乎绝对依赖细胞外钙,而凝血酶诱导的释放仅部分依赖钙。过夜培养后,对凝血酶的反应不变,而对离子载体的ATP释放持续增加(p<0.01)。通过比较最大可释放ATP与总细胞ATP含量,确定巨核细胞中ATP的储存池仅占巨核细胞总ATP的2%-6%,而豚鼠血小板中的ATP储存池为20%-30%。这种差异可能反映了ATP进一步进入储存池隔室或随着巨核细胞达到完全成熟,细胞识别并充分响应血小板刺激的能力增强。

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