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对健康志愿者给予粒细胞集落刺激因子:对循环中性粒细胞的即时激活作用分析

Granulocyte colony-stimulating factor administration to healthy volunteers: analysis of the immediate activating effects on circulating neutrophils.

作者信息

de Haas M, Kerst J M, van der Schoot C E, Calafat J, Hack C E, Nuijens J H, Roos D, van Oers R H, von dem Borne A E

机构信息

Central Laboratory of The Netherlands Red Cross Blood Transfusion Service, Amsterdam.

出版信息

Blood. 1994 Dec 1;84(11):3885-94.

PMID:7524751
Abstract

In four healthy volunteers, we analyzed in detail the immediate in vivo effects on circulating neutrophils of subcutaneous administration of 300 micrograms of granulocyte colony-stimulating factor (G-CSF). Neutrophil activation was assessed by measurement of degranulation. Mobilization of secretory vesicles was shown by a decrease in leukocyte alkaline phosphatase content of the circulating neutrophils. Furthermore, shortly postinjection, Fc gamma RIII was found to be upregulated from an intracellular pool that we identified by immunoelectron microscopy as secretory vesicles. Intravascular release of specific granules was shown by increased plasma levels of lactoferrin and by upregulation of the expression of CD66b and CD11b on circulating neutrophils. Moreover, measurement of fourfold elevated plasma levels of elastase, bound to its physiologic inhibitor alpha 1-antitrypsin, indicated mobilization of azurophil granules. However, no expression of CD63, a marker of azurophil granules, was observed on circulating neutrophils. G-CSF--induced mobilization of secretory vesicles and specific granules could be mimicked in whole blood cultures in vitro, in contrast to release of azurophil granules. Therefore, we postulate that the most activated neutrophils leave the circulation, as observed shortly postinjection, and undergo subsequent stimulation in the endothelial microenvironment, resulting in mobilization of azurophil granules. Our data demonstrate that G-CSF should be regarded as a potent immediate activator of neutrophils in vivo.

摘要

在4名健康志愿者中,我们详细分析了皮下注射300微克粒细胞集落刺激因子(G-CSF)对循环中性粒细胞的即时体内效应。通过测量脱颗粒来评估中性粒细胞的活化。循环中性粒细胞中白细胞碱性磷酸酶含量的降低表明分泌囊泡的动员。此外,注射后不久,发现FcγRIII从一个我们通过免疫电子显微镜鉴定为分泌囊泡的细胞内池上调。乳铁蛋白血浆水平升高以及循环中性粒细胞上CD66b和CD11b表达上调表明特异性颗粒的血管内释放。此外,与生理抑制剂α1-抗胰蛋白酶结合的弹性蛋白酶血浆水平升高四倍的测量结果表明嗜天青颗粒的动员。然而,在循环中性粒细胞上未观察到嗜天青颗粒的标志物CD63的表达。与嗜天青颗粒的释放相反,G-CSF诱导的分泌囊泡和特异性颗粒的动员可以在体外全血培养中模拟。因此,我们推测,如注射后不久所观察到的,最活化的中性粒细胞离开循环,并在内皮微环境中经历随后的刺激,导致嗜天青颗粒的动员。我们的数据表明,G-CSF应被视为体内中性粒细胞的强效即时激活剂。

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