Desterke Christophe, Martinaud Christophe, Guerton Bernadette, Pieri Lisa, Bogani Costanza, Clay Denis, Torossian Frederic, Lataillade Jean-Jacques, Hasselbach Hans C, Gisslinger Heinz, Demory Jean-Loup, Dupriez Brigitte, Boucheix Claude, Rubinstein Eric, Amsellem Sophie, Vannucchi Alessandro M, Le Bousse-Kerdilès Marie-Caroline
INSERM UMR-S1197, Paul Brousse Hospital, Paris-Sud University, Villejuif, France INSERM UMS33, Paul Brousse Hospital, Paris-Sud University, Villejuif, France.
INSERM UMR-S1197, Paul Brousse Hospital, Paris-Sud University, Villejuif, France CTS of Army, Percy Hospital, Clamart, France.
Haematologica. 2015 Jun;100(6):757-67. doi: 10.3324/haematol.2014.118497. Epub 2015 Apr 3.
Primary myelofibrosis is characterized by clonal myeloproliferation, dysmegakaryopoiesis, extramedullary hematopoiesis associated with myelofibrosis and altered stroma in the bone marrow and spleen. The expression of CD9, a tetraspanin known to participate in megakaryopoiesis, platelet formation, cell migration and interaction with stroma, is deregulated in patients with primary myelofibrosis and is correlated with stage of myelofibrosis. We investigated whether CD9 participates in the dysmegakaryopoiesis observed in patients and whether it is involved in the altered interplay between megakaryocytes and stromal cells. We found that CD9 expression was modulated during megakaryocyte differentiation in primary myelofibrosis and that cell surface CD9 engagement by antibody ligation improved the dysmegakaryopoiesis by restoring the balance of MAPK and PI3K signaling. When co-cultured on bone marrow mesenchymal stromal cells from patients, megakaryocytes from patients with primary myelofibrosis displayed modified behaviors in terms of adhesion, cell survival and proliferation as compared to megakaryocytes from healthy donors. These modifications were reversed after antibody ligation of cell surface CD9, suggesting the participation of CD9 in the abnormal interplay between primary myelofibrosis megakaryocytes and stroma. Furthermore, silencing of CD9 reduced CXCL12 and CXCR4 expression in primary myelofibrosis megakaryocytes as well as their CXCL12-dependent migration. Collectively, our results indicate that CD9 plays a role in the dysmegakaryopoiesis that occurs in primary myelofibrosis and affects interactions between megakaryocytes and bone marrow stromal cells. These results strengthen the "bad seed in bad soil" hypothesis that we have previously proposed, in which alterations of reciprocal interactions between hematopoietic and stromal cells participate in the pathogenesis of primary myelofibrosis.
原发性骨髓纤维化的特征为克隆性骨髓增殖、巨核细胞生成异常、与骨髓纤维化相关的髓外造血以及骨髓和脾脏中基质的改变。CD9是一种四跨膜蛋白,已知参与巨核细胞生成、血小板形成、细胞迁移以及与基质的相互作用,在原发性骨髓纤维化患者中其表达失调,且与骨髓纤维化的分期相关。我们研究了CD9是否参与患者中观察到的巨核细胞生成异常,以及它是否参与巨核细胞与基质细胞之间改变的相互作用。我们发现,在原发性骨髓纤维化中,巨核细胞分化过程中CD9表达受到调控,通过抗体连接使细胞表面CD9结合可恢复MAPK和PI3K信号平衡,从而改善巨核细胞生成异常。当与原发性骨髓纤维化患者的骨髓间充质基质细胞共培养时,与健康供体的巨核细胞相比,原发性骨髓纤维化患者的巨核细胞在黏附、细胞存活和增殖方面表现出改变的行为。细胞表面CD9抗体连接后,这些改变得以逆转,表明CD9参与原发性骨髓纤维化巨核细胞与基质之间的异常相互作用。此外,CD9沉默降低了原发性骨髓纤维化巨核细胞中CXCL12和CXCR4的表达以及它们依赖CXCL12的迁移。总体而言,我们的结果表明,CD9在原发性骨髓纤维化中发生的巨核细胞生成异常中起作用,并影响巨核细胞与骨髓基质细胞之间的相互作用。这些结果强化了我们之前提出的“坏土中的坏种子”假说,即造血细胞与基质细胞之间相互作用的改变参与了原发性骨髓纤维化的发病机制。