Abstract

Neutrophils play a crucial role in host defence. In response to a variety of inflammatory stimulation, they form neutrophil extracellular traps (NETs). NETs are extracellular structures composed of chromatin fibers decorated with antimicrobial proteins and developing studies indicate that NETs contribute to extracellular microbial killing. While the intracellular signaling pathways that regulate NET formation remain largely unknown, there is growing evidence that generation of reactive oxygen species (ROS) is a key event for NET formation. The Rab family small GTPase Rab27a is an important component of the secretory machinery of azurophilic granules in neutrophils. However, the precise mechanism of NET formation and whether or not Rab27a contributes to this process are unknown. Using neutrophil-like differentiated HL60 cells, we show here that Rab27a plays an essential role in both phorbol myristate acetate (PMA)- and Candida albicans-induced NET formation by regulating ROS production. Rab27a-knockdown inhibited ROS-positive phagosome formation during complement-mediated phagocytosis. To investigate the role of Rab27a in neutrophil function in detail, both primary human neutrophils and neutrophil-like differentiated HL60 cells were treated with PMA, and NET formation process was assessed by measurement of release of histone H3 into the medium, citrullination of the arginine in position 3 of histone H4 and chase of the nuclear change of the living cells in the co-existence of both cell-permeable and -impermeable nuclear indicators. PMA-induced NET formation occured sequentially in both neutrophil-like differentiated HL60 cells and primary neutrophils, and Rab27a-knockdown clearly inhibited NET formation in association with reduced ROS production. We also found that serum-treated Candida albicans triggers NET formation in a ROS-dependent manner, and that Rab27a-knockdown inhibits this process as well. Our findings demonstrate that Rab27a plays an important role in NET formation induced by both Candida albicans infection and PMA treatment by regulating ROS production.

Highlights

  • Rab27a is a member of the Rab family of small GTPase proteins

  • We investigated the role of Rab27a in neutrophil function using primary human neutrophils and neutrophil-like differentiated HL60 cells and found that this protein is essential for both phorbol myristate acetate (PMA)- and Candida albicans (C. albicans)-induced neutrophil extracellular traps (NETs) formation by up-regulating reactive oxygen species (ROS) producton mediated by NADPH oxidase

  • To elucidate the role of Rab27a in neutrophil function, HL60 cells, Rab27a-knockdown cells transfected with shRNA-Rab27a using a lentiviral system, and control-shRNA transferred HL60 cells were treated with all-trans retinoic acid (ATRA) and allowed to differentiate into neutrophil-like cells for 3 days [6,20]

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Summary

Introduction

Rab27a is a member of the Rab family of small GTPase proteins. Rab27a is involved in the exocytosis of secretory granules in melanocytes and cytotoxic T lymphocytes. Mutations in Rab27a cause type-2 Griscelli syndrome, which is characterized by pigment dilution and defects in cytotoxic granule transport, and aslo cause macrophage activation syndrome (known as hemophagocytic syndrome, HS) [3,4,5]. Rab27a plays a critical role in innate immune defenses against invading microorganisms. We previously demonstrated that Rab27a negatively regulates complementmediated phagocytic activity in association with F-actin remodeling in macrophages [6]. Catz and colleagues intensively studied the important role of Rab27a in myeloperoxidase (MPO) secretion in neutrophil azurophilic granules [8]

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