炎症
骨髓
造血
纤维化
癌症研究
免疫学
生物
医学
病理
干细胞
遗传学
作者
Hélène F.E. Gleitz,Aurélien Dugourd,Nils B. Leimkühler,Inge Snoeren,Stijn N.R. Fuchs,Sylvia Menzel,Susanne Ziegler,Nicolaus Kröger,Ioanna Triviai,Guntram Büsche,Hans Kreipe,Bella Banjanin,Jessica E. Pritchard,Remco M. Hoogenboezem,Eric M. Bindels,Neele Schumacher,Stefan Rose‐John,Shannon Elf,Julio Sáez-Rodríguez,Rafael Kramann,Rebekka K. Schneider
出处
期刊:Blood
[American Society of Hematology]
日期:2020-07-29
卷期号:136 (18): 2051-2064
被引量:73
标识
DOI:10.1182/blood.2019004095
摘要
Primary myelofibrosis (PMF) is a myeloproliferative neoplasm (MPN) that leads to progressive bone marrow (BM) fibrosis. Although the cellular mutations involved in the pathogenesis of PMF have been extensively investigated, the sequential events that drive stromal activation and fibrosis by hematopoietic-stromal cross-talk remain elusive. Using an unbiased approach and validation in patients with MPN, we determined that the differential spatial expression of the chemokine CXCL4/platelet factor-4 marks the progression of fibrosis. We show that the absence of hematopoietic CXCL4 ameliorates the MPN phenotype, reduces stromal cell activation and BM fibrosis, and decreases the activation of profibrotic pathways in megakaryocytes, inflammation in fibrosis-driving cells, and JAK/STAT activation in both megakaryocytes and stromal cells in 3 murine PMF models. Our data indicate that higher CXCL4 expression in MPN has profibrotic effects and is a mediator of the characteristic inflammation. Therefore, targeting CXCL4 might be a promising strategy to reduce inflammation in PMF.
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