4.5 Article

Human monocytes store and secrete preformed CCL5, independent of de novo protein synthesis

期刊

JOURNAL OF LEUKOCYTE BIOLOGY
卷 111, 期 3, 页码 573-583

出版社

OXFORD UNIV PRESS
DOI: 10.1002/JLB.3A0820-522RR

关键词

CCL5; RANTES; cytokine secretion; cytokines; chemokines; inflammation; late endosome; LPS; monocytes; recycling endosome

资金

  1. Natural Sciences and Engineering Research Council (NSERC)

向作者/读者索取更多资源

This study identifies a previously undescribed reservoir of preformed chemokine CCL5 in circulating human monocytes, allowing for immediate secretion of immune mediators upon activation, bypassing the time lag associated with de novo synthesis of cytokines. This finding implicates endosomal compartments in the intracellular storage and trafficking of CCL5 in monocytes.
Monocytes are a subset of circulating peripheral blood mononuclear cells with diverse roles in immunity, including sentinel roles in cytokine secretion. Conventionally, cytokines require an inductive stimulus for their expression and secretion, resulting in a time lag from the time of stimulation to when the proteins are packaged and secreted. Because cytokines are the main communicators in the immune system, their temporal expression is a key factor in coordinating responses to efficiently resolve infection. Herein, we identify that circulating human monocytes contain preformed cytokines that are stored intracellularly, in both resting and activated states. Having preformed cytokines bypasses the time lag associated with de novo synthesis, allowing monocytes to secrete immune mediators immediately upon activation or sensing of microbe-associated molecular patterns. We demonstrate here that, out of several cytokines evaluated, human monocytes contain a previously undescribed reservoir of the preformed chemokine CCL5. Furthermore, we showed that CCL5 could be secreted from monocytes treated with the protein synthesis inhibitor (cycloheximide) and Golgi blocker (brefeldin A). We examined the possibility for uptake of extracellular CCL5 from platelet aggregates and observed no significant levels of platelet binding to our enriched monocyte preparations, indicating that the source of preformed CCL5 was not from platelets. Preformed CCL5 was observed to be distributed throughout the cytoplasm and partially colocalized with CD63+ and Rab11A+ membranes, implicating endosomal compartments in the intracellular storage and trafficking of CCL5.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据