Publication: Reduced PU.1 expression underlies aberrant neutrophil maturation and function in b-Thalassemia mice and patients
Issued Date
2017-06-08
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ISSN
15280020
00064971
00064971
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2-s2.0-85020704965
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Mahidol University
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SCOPUS
Bibliographic Citation
Blood. Vol.129, No.23 (2017), 3087-3099
Suggested Citation
Panjaree Siwaponanan, Jurre Ynze Siegers, Razi Ghazali, Thian Ng, Bradley Mccoll, Garrett Zhen Wei Ng, Philip Sutton, Nancy Wang, Isabelle Ooi, Chayada Thiengtavor, Suthat Fucharoen, Pornthip Chaichompoo, Saovaros Svasti, Odilia Wijburg, Jim Vadolas Reduced PU.1 expression underlies aberrant neutrophil maturation and function in b-Thalassemia mice and patients. Blood. Vol.129, No.23 (2017), 3087-3099. doi:10.1182/blood-2016-07-730135 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/41843
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Title
Reduced PU.1 expression underlies aberrant neutrophil maturation and function in b-Thalassemia mice and patients
Abstract
© 2017 by The American Society of Hematology. β-Thalassemia is associated with several abnormalities of the innate immune system. Neutrophils in particular are defective, predisposing patients to life-Threatening bacterial infections. The molecular and cellular mechanisms involved in impaired neutrophil function remain incompletely defined. We used the Hbbth3/+ β-Thalassemia mouse and hemoglobin E (HbE)/β-Thalassemia patients to investigate dysregulated neutrophil activity. Mature neutrophils from Hbbth3/1 mice displayed a significant reduction in chemotaxis, opsonophagocytosis, and production of reactive oxygen species, closely mimicking the defective immune functions observed in β-Thalassemia patients. In Hbbth3/1 mice, the expression of neutrophil CXCR2, CD11b, and reduced NAD phosphate oxidase components (p22phox, p67phox, and gp91phox) were significantly reduced.Morphological analysis of Hbbth3/1 neutrophils showed that a large percentage of mature phenotype neutrophils (Ly6GhiLy6Clow) appeared as band form cells, and a striking expansion of immature (Ly6GlowLy6Clow) hyposegmented neutrophils, consisting mainly of myelocytes and metamyelocytes, was noted. Intriguingly, expression of an essential mediator of neutrophil terminal differentiation, the ets transcription factor PU.1, was significantly decreased in Hbbth3/1 neutrophils. In addition, in vivo infection with Streptococcus pneumoniae failed to induce PU.1 expression or upregulate neutrophil effector functions in Hbbth3/1 mice. Similar changes to neutrophil morphology and PU.1 expression were observed in splenectomized and nonsplenectomized HbE/β-Thalassemia patients. This study provides amechanistic insight into defective neutrophil maturation in β-Thalassemia patients, which contributes to deficiencies in neutrophil effector functions.