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Megakaryocytes contribute to the bone marrow-matrix environment by expressing fibronectin type IV collagen and laminin

机译:巨核细胞通过表达纤连蛋白IV型胶原和层粘连蛋白来促进骨髓基质环境

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摘要

Megakaryocytes associate with the bone marrow vasculature where they convert their cytoplasm into proplatelets that protrude through the vascular endothelium into the lumen and release platelets. The extracellular matrix (ECM) microenvironment plays a critical role in regulating these processes. In this work we demonstrate that, among bone marrow ECM components, fibronectin, type IV collagen and laminin are the most abundant around bone marrow sinusoids and constitute a peri-cellular matrix surrounding megakaryocytes. Most importantly, we report, for the first time, that megakaryocytes express components of the basement membrane and that these molecules contribute to the regulation of megakaryocyte development and bone marrow ECM homeostasis both in vitro and in vivo. In vitro, fibronectin induced a three-fold increase in the proliferation rate of mouse hematopoietic stem cells leading to higher megakaryocyte output with respect to cells treated only with thrombopoietin or other matrices. However, megakaryocyte ploidy level in fibronectin-treated cultures was significantly reduced. Stimulation with type IV collagen resulted in a 1.4-fold increase in megakaryocyte output, while all tested matrices supported proplatelet formation to a similar extent in megakaryocytes derived from fetal liver progenitor cells. In vivo, megakaryocyte expression of fibronectin and basement membrane components was up-regulated during bone marrow reconstitution upon 5-fluorouracil induced myelosuppression, while only type IV collagen resulted up-regulated upon induced thrombocytopenia. In conclusion, this work demonstrates that ECM components impact megakaryocyte behavior differently during their differentiation and highlights a new role for megakaryocyte as ECM-producing cells for the establishment of cell niches during bone marrow regeneration.
机译:巨核细胞与骨髓脉管系统相关联,在那里它们将其细胞质转化为前血小板,该前血小板通过血管内皮突出进入内腔并释放血小板。细胞外基质(ECM)微环境在调节这些过程中起着至关重要的作用。在这项工作中,我们证明,在骨髓ECM成分中,纤连蛋白,IV型胶原和层粘连蛋白在骨髓正弦曲线周围最丰富,并构成巨核细胞周围的细胞周围基质。最重要的是,我们首次报道了巨核细胞表达基底膜的成分,并且这些分子在体外和体内均有助于巨核细胞的发育和骨髓ECM稳态的调节。在体外,与仅用血小板生成素或其他基质处理的细胞相比,纤连蛋白诱导小鼠造血干细胞的增殖速率增加了三倍,从而导致更高的巨核细胞输出。但是,纤连蛋白处理的培养物中巨核细胞倍性水平显着降低。 IV型胶原蛋白的刺激导致巨核细胞输出增加1.4倍,而所有测试基质在源自胎儿肝祖细胞的巨核细胞中均支持血小板原形成。在体内,在5-氟尿嘧啶诱导的骨髓抑制后的骨髓重建过程中,纤连蛋白和基底膜成分的巨核细胞表达被上调,而诱导的血小板减少症则仅IV型胶原被上调。总之,这项工作表明,ECM组分在分化过程中对巨核细胞行为的影响不同,并突出了巨核细胞作为产生ECM的细胞在骨髓再生过程中建立细胞壁的新作用。

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