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The Application of Dextran Sedimentation as an Initial Step in Neutrophil Purification Promotes Their Stimulation due to the Presence of Monocytes

机译:由于单核细胞的存在右旋糖酐沉淀作为中性粒细胞纯化的初始步骤的应用促进了它们的刺激。

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摘要

The purification of human neutrophils for in vitro studies is challenging as they are easily activated through ex vivo manipulations. The technique of erythrocyte sedimentation combined with density gradient centrifugation remains widely practiced and was the subject of this study. Since in the sedimentation step the leukocytes are incubated with dextran, we have raised the likelihood that cellular activation would occur with mediator release leading to neutrophil activation. By comparing the activity of neutrophils purified from whole blood by the classical 2-step method of dextran sedimentation followed by low-density Ficoll-Hypaque (1.077 g/mL) medium, and the 1-step high-density Ficoll-Hypaque (1.114 g/mL) gradient centrifugation, we found that neutrophils from the 2-step method had a significant increase in cell surface CD11b expression and CD62L shedding and a marked increase in adhesion. Decreased random migration and chemotaxis and raised baseline oxidative burst activity were also observed. The effect was not specific to dextran, as using Ficoll for erythrocyte sedimentation replicated the elevated neutrophil adherence. Through the depletion of monocytes, lymphocytes, and platelets prior to sedimentation, we deduced that monocytes were responsible for the neutrophil activation. Our findings suggest that care needs to be exercised in choosing the method of neutrophil purification for functional studies.
机译:纯化人类嗜中性粒细胞以进行体外研究具有挑战性,因为它们可以通过离体操作轻松激活。红细胞沉降结合密度梯度离心的技术仍被广泛实践,并且是本研究的主题。由于在沉淀步骤中将白细胞与右旋糖酐一起孵育,我们提高了通过激活介质释放导致中性粒细胞激活而发生细胞激活的可能性。通过比较经典的两步法右旋糖酐沉淀法,然后再用低密度Ficoll-Hypaque(1.077 / g / mL)培养基和1步高密度Ficoll-Hypaque(1.114 g)从全血中纯化的嗜中性粒细胞的活性/ mL)梯度离心,我们发现2步法得到的嗜中性粒细胞细胞表面CD11b表达和CD62L脱落显着增加,并且粘附力显着增加。还观察到随机迁移和趋化性降低,基线氧化爆发活性升高。该作用对葡聚糖不是特异的,因为使用Ficoll进行红细胞沉降可以复制嗜中性粒细胞的粘附性。通过沉淀之前单核细胞,淋巴细胞和血小板的消耗,我们推断出单核细胞是中性粒细胞活化的原因。我们的发现表明,在选择功能研究中性粒细胞纯化方法时需要谨慎。

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