The expanding family of neutrophil-derived extracellular vesicles
被引:16
|
作者:
Marki, Alex
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机构:
AstraZeneca, Gaithersburg, MD USAAstraZeneca, Gaithersburg, MD USA
Marki, Alex
[1
]
Ley, Klaus
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机构:
Univ Calif San Diego, La Jolla Inst Immunol, La Jolla, CA 92093 USA
Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
Univ Calif San Diego, Inst Engn Med, La Jolla, CA 92093 USAAstraZeneca, Gaithersburg, MD USA
Ley, Klaus
[2
,3
,4
]
机构:
[1] AstraZeneca, Gaithersburg, MD USA
[2] Univ Calif San Diego, La Jolla Inst Immunol, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Inst Engn Med, La Jolla, CA 92093 USA
Neutrophils are immune cells involved in several inflammatory and homeostatic processes. Their capacity to release cargo can be classified based on whether the cargo is released on its own, or in conjunction with plasma membrane structures. Examples of plasma membrane-free secretion modes are degranulation, neutrophil extracellular trap (NET) release, and cytokine release through inflammasome formation. The most studied membrane-covered neutrophil-derived structures are exosomes and ectosomes that are collectively called extracellular vesicles (EV). Apoptotic vesicles are another recognized EV subtype. Over the last decade, additional membrane-covered neutrophil-derived structures were characterized: migratory cytoplasts, migrasomes, and elongated neutrophil-derived structures (ENDS). All these structures are smaller than the neutrophils, cannot reproduce themselves, and thus meet the latest consensus definition of EVs. In this review, we focus on the less well-studied neutrophil EVs: apoptotic vesicles, cytoplasts, migrasomes, and ENDS.