Sedgwick J B, Shikama Y, Nagata M, Brener K, Busse W W
Department of Medicine, University of Wisconsin, Madison, USA.
J Immunol Methods. 1996 Oct 30;198(1):15-24. doi: 10.1016/0022-1759(96)00139-1.
Studies of in vitro eosinophil function are dependent on efficient and reliable methods of cell isolation. Protocols using Percoll or metrizamide density gradients have been of limited use in isolating peripheral blood eosinophils in sufficient numbers and purity from subjects with normal or only slightly elevated eosinophil counts, thereby restricting comparative studies to preparations from hypereosinophilic subjects. Recently, a method utilizing negative selection by anti-CD16 coated magnetic beads has greatly improved eosinophil isolation by dramatically increased yields and purity. However, little is known as to the differential effect of various isolation methods on the functional activity of eosinophils. In this study, eosinophils were isolated by either discontinuous multiple density Percoll gradients or anti-CD16-coated magnetic beads: several functional activities were then compared using cells obtained by the two methods of isolation. Compared with Percoll isolated eosinophils, anti-CD16 bead separated eosinophils had significantly increased baseline and stimulated LTC4 production, spontaneous O2- generation, and expression of specific cell surface markers. No significant difference was observed in the cells' in vitro survival and adhesion. Such differences may be due to the isolation of eosinophils of all densities by anti-CD16 beads, or the effect of neutrophils interacting with the beads to release eosinophil agonists or primers. Alternatively, the Percoll gradient method with the eosinophils' exposure to dextran and Ficoll-Hypaque may affect subsequent cell function. Therefore, comparison of eosinophil function between cells isolated by different protocols must be considered before concluding which is the true measure of in vivo cell function.
体外嗜酸性粒细胞功能的研究依赖于高效且可靠的细胞分离方法。使用Percoll或甲泛葡胺密度梯度的方案在从嗜酸性粒细胞计数正常或仅略有升高的受试者中分离出足够数量和纯度的外周血嗜酸性粒细胞方面用途有限,从而将比较研究限制在来自嗜酸性粒细胞增多症受试者的制剂上。最近,一种利用抗CD16包被磁珠进行阴性选择的方法通过显著提高产量和纯度极大地改善了嗜酸性粒细胞的分离。然而,对于各种分离方法对嗜酸性粒细胞功能活性的差异影响知之甚少。在本研究中,通过不连续多重密度Percoll梯度或抗CD16包被磁珠分离嗜酸性粒细胞:然后使用通过两种分离方法获得的细胞比较几种功能活性。与Percoll分离的嗜酸性粒细胞相比,抗CD16磁珠分离的嗜酸性粒细胞的基线和刺激后的LTC4产生、自发O2-生成以及特定细胞表面标志物的表达显著增加。在细胞的体外存活和黏附方面未观察到显著差异。这些差异可能是由于抗CD16磁珠分离了所有密度的嗜酸性粒细胞,或者是中性粒细胞与磁珠相互作用释放嗜酸性粒细胞激动剂或引物的作用。或者,Percoll梯度方法以及嗜酸性粒细胞暴露于葡聚糖和聚蔗糖-泛影葡胺可能会影响随后的细胞功能。因此,在确定哪种方法是体内细胞功能的真正衡量标准之前,必须考虑比较不同方案分离的细胞之间的嗜酸性粒细胞功能。