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骨髓纤维化患者的脾脏中存在缺陷的间充质基质细胞。

The spleen of patients with myelofibrosis harbors defective mesenchymal stromal cells.

机构信息

Pediatric Onco-Hematology/Cell Factory, IRCCS Policlinico San Matteo Foundation, Pavia, Italy.

Department of Molecular Medicine, University of Pavia, Pavia, Italy.

出版信息

Am J Hematol. 2018 May;93(5):615-622. doi: 10.1002/ajh.25047. Epub 2018 Feb 8.

Abstract

Splenic hematopoiesis is a major feature in the course of myelofibrosis (MF). In fact, the spleen of patients with MF contains malignant hematopoietic stem cells retaining a complete differentiation program, suggesting both a pivotal role of the spleen in maintaining the disease and a tight regulation of hematopoiesis by the splenic microenvironment, in particular by mesenchymal stromal cells (MSCs). Little is known about splenic MSCs (Sp-MSCs), both in normal and in pathological context. In this work, we have in vitro expanded and characterized Sp-MSCs from 25 patients with MF and 13 healthy subjects (HS). They shared similar phenotype, growth kinetics, and differentiation capacity. However, MF Sp-MSCs expressed significant lower levels of nestin, and favored megakaryocyte (Mk) differentiation in vitro at a larger extent than their normal counterpart. Moreover, they showed a significant upregulation of matrix metalloprotease 2 (MMP2) and fibronectin 1 (FN1) genes both at mRNA expression and at protein level, and, finally, developed genetic abnormalities which were never detected in HS-derived Sp-MSCs. Our data point toward the existence of a defective splenic niche in patients with MF that could be responsible of some pathological features of the disease, including the increased trafficking of CD34+ cells and the expansion of the megakaryocytic lineage.

摘要

脾造血是骨髓纤维化 (MF) 病程中的一个主要特征。事实上,MF 患者的脾脏中含有保留完整分化程序的恶性造血干细胞,这表明脾脏在维持疾病方面起着关键作用,并且脾脏微环境(特别是间质基质细胞 [MSCs])对造血有严格的调控作用。在正常和病理情况下,人们对脾 MSCs(Sp-MSCs)知之甚少。在这项工作中,我们从 25 名 MF 患者和 13 名健康受试者 (HS) 中体外扩增和鉴定了 Sp-MSCs。它们具有相似的表型、生长动力学和分化能力。然而,MF Sp-MSCs 表达的巢蛋白水平明显较低,并且在体外比其正常对应物更倾向于巨核细胞 (Mk) 分化。此外,它们在 mRNA 表达和蛋白水平上均显著上调基质金属蛋白酶 2 (MMP2) 和纤维连接蛋白 1 (FN1) 基因,最终发展出在 HS 衍生的 Sp-MSCs 中从未检测到的遗传异常。我们的数据表明,MF 患者存在脾脏龛位缺陷,这可能是该疾病一些病理特征的原因,包括 CD34+细胞的增加转移和巨核细胞系的扩增。

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