Partouche Shirly, Goldberg Idan, Halperin Erez, Atamna Bahaa, Shacham-Abulafia Adi, Shapira Saar, Samara Aladin, Gover-Proaktor Ayala, Leader Avi, Spectre Galia, Raanani Pia, Granot Galit, Wolach Ofir
Felsenstein Medical Research Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva 4941492, Israel.
Institute of Hematology, Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva 4941492, Israel.
Int J Mol Sci. 2024 Dec 16;25(24):13473. doi: 10.3390/ijms252413473.
Neutrophils and neutrophil extracellular traps (NETs) contribute to thrombosis and hyperinflammation in myeloproliferative neoplasms (MPN). High-density neutrophils (HDNs) and low-density neutrophils (LDNs) have recently been characterized as distinct neutrophil sub-populations with distinct morphological and functional properties. We aim to study the kinetics of NET formation and inhibition with interferon-α (IFNα) in neutrophils derived from patients with MPN as compared to matched healthy controls. Ex vivo NET formation was assessed by neutrophil-elastase activity, neutrophil-associated nucleosomes, myeloperoxidase (MPO), and citrullinated histone H3 content. IFNα significantly inhibited NET formation in neutrophils derived from MPN patients. Neutrophil sub-population analysis demonstrated that HDNs drive the increase in NET formation as compared to LDNs in patients and in healthy controls and are effectively inhibited by IFNα, an effect that is lost in LDNs. In conclusion, we demonstrate that in MPN, HDNs drive excess NET formation and are more sensitive to IFNα inhibition. These observations uncover unique neutrophil sub-population biology and dynamics in MPN.
中性粒细胞和中性粒细胞胞外诱捕网(NETs)在骨髓增殖性肿瘤(MPN)中促成血栓形成和过度炎症反应。高密度中性粒细胞(HDNs)和低密度中性粒细胞(LDNs)最近被鉴定为具有不同形态和功能特性的独特中性粒细胞亚群。我们旨在研究与匹配的健康对照相比,MPN患者来源的中性粒细胞中NET形成的动力学以及干扰素-α(IFNα)对其的抑制作用。通过中性粒细胞弹性蛋白酶活性、中性粒细胞相关核小体、髓过氧化物酶(MPO)和瓜氨酸化组蛋白H3含量评估体外NET形成。IFNα显著抑制MPN患者来源的中性粒细胞中的NET形成。中性粒细胞亚群分析表明,与患者和健康对照中的LDNs相比,HDNs驱动NET形成增加,并且被IFNα有效抑制,而LDNs则无此效应。总之,我们证明在MPN中,HDNs驱动过量的NET形成并且对IFNα抑制更敏感。这些观察结果揭示了MPN中独特的中性粒细胞亚群生物学和动力学。