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人嗜酸性粒细胞表达功能性 CCR7。

Human eosinophils express functional CCR7.

机构信息

Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

出版信息

Am J Respir Cell Mol Biol. 2013 Jun;48(6):758-64. doi: 10.1165/rcmb.2012-0499OC.

Abstract

Human eosinophils display directed chemotactic activity toward an array of soluble chemokines. Eosinophils have been observed to migrate to draining lymph nodes in experimental models of allergic inflammation, yet it is unknown whether eosinophils express CCR7, a key chemokine receptor in coordinating leukocyte trafficking to lymph nodes. The purpose of this study is to demonstrate expression of CCR7 by human eosinophils and functional responses to CCL19 and CCL21, the known ligands of CCR7. Human eosinophils were purified by negative selection from healthy donors. CCR7 expression of freshly purified, unstimulated eosinophils and of IL-5-primed eosinophils was determined by flow cytometry and Western blot. Chemotaxis to CCL19 and CCL21 was measured in transwell assays. Shape changes to CCL19 and CCL21 were analyzed by flow cytometry and microscopy. Calcium fluxes of fluo-4 AM-loaded eosinophils were recorded by flow cytometry after chemokine stimulation. ERK phosphorylation of CCL19- and CCL21-stimulated eosinophils was measured by Western blot and Luminex assay. Human eosinophils expressed CCR7 as demonstrated by flow cytometry and Western blots. Eosinophils exhibited detectable cell surface expression of CCR7. IL-5-primed eosinophils exhibited chemotaxis toward CCL19 and CCL21 in a dose-dependent fashion. Upon stimulation with CCL19 or CCL21, IL-5-primed eosinophils demonstrated dose-dependent shape changes with polarization of F-actin and exhibited calcium influxes. Finally, primed eosinophils stimulated with CCL19 or CCL21 exhibited increased phosphorylation of ERK in response to both CCR7 ligands. We demonstrate that human eosinophils express CCR7 and have multipotent responses to the known ligands of CCR7.

摘要

人类嗜酸性粒细胞对一系列可溶性趋化因子表现出定向趋化活性。在过敏炎症的实验模型中,观察到嗜酸性粒细胞迁移到引流淋巴结,但尚不清楚嗜酸性粒细胞是否表达 CCR7,CCR7 是协调白细胞向淋巴结迁移的关键趋化因子受体。本研究旨在证明人类嗜酸性粒细胞表达 CCR7 及其对 CCL19 和 CCL21 的功能反应,CCL19 和 CCL21 是 CCR7 的已知配体。通过阴性选择从健康供体中纯化人嗜酸性粒细胞。通过流式细胞术和 Western blot 测定新鲜纯化、未刺激的嗜酸性粒细胞和 IL-5 预刺激的嗜酸性粒细胞中 CCR7 的表达。通过 Transwell 测定法测定对 CCL19 和 CCL21 的趋化作用。通过流式细胞术和显微镜分析 CCL19 和 CCL21 的形状变化。用趋化因子刺激后,通过流式细胞术记录负载 fluo-4 AM 的嗜酸性粒细胞的钙通量。通过 Western blot 和 Luminex 测定法测定 CCL19 和 CCL21 刺激的嗜酸性粒细胞的 ERK 磷酸化。流式细胞术和 Western blot 证明人嗜酸性粒细胞表达 CCR7。嗜酸性粒细胞表现出可检测的细胞表面 CCR7 表达。IL-5 预刺激的嗜酸性粒细胞以剂量依赖性方式对 CCL19 和 CCL21 表现出趋化性。用 CCL19 或 CCL21 刺激后,IL-5 预刺激的嗜酸性粒细胞表现出剂量依赖性的形状变化,肌动蛋白呈极化,并表现出钙内流。最后,用 CCL19 或 CCL21 刺激的预刺激嗜酸性粒细胞对两种 CCR7 配体均表现出 ERK 磷酸化增加。我们证明人类嗜酸性粒细胞表达 CCR7 并对 CCR7 的已知配体具有多能反应。

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本文引用的文献

1
Isolation of human eosinophils.人嗜酸性粒细胞的分离
Curr Protoc Immunol. 2012 Aug;Chapter 7:7.31.1-7.31.8. doi: 10.1002/0471142735.im0731s98.
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CCR7 is involved in the migration of neutrophils to lymph nodes.CCR7 参与中性粒细胞向淋巴结的迁移。
Blood. 2011 Jan 27;117(4):1196-204. doi: 10.1182/blood-2009-11-254490. Epub 2010 Nov 4.

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