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血小板生成素/TGF-β1循环调节巨核细胞细胞外基质成分的合成。

Thrombopoietin/TGF-β1 Loop Regulates Megakaryocyte Extracellular Matrix Component Synthesis.

作者信息

Abbonante Vittorio, Di Buduo Christian A, Gruppi Cristian, Malara Alessandro, Gianelli Umberto, Celesti Giuseppe, Anselmo Achille, Laghi Luigi, Vercellino Marco, Visai Livia, Iurlo Alessandra, Moratti Remigio, Barosi Giovanni, Rosti Vittorio, Balduini Alessandra

机构信息

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

Laboratory of Biotechnology, IRCCS San Matteo Foundation, Pavia, Italy.

出版信息

Stem Cells. 2016 Apr;34(4):1123-33. doi: 10.1002/stem.2285. Epub 2016 Jan 29.

Abstract

Extracellular matrix (ECM) components initiate crucial biochemical and biomechanical cues that are required for bone marrow homeostasis. In our research, we prove that a peri-cellular matrix composed primarily of type III and type IV collagens, and fibronectin surrounds human megakaryocytes in the bone marrow. The data we collected support the hypothesis that bone marrow megakaryocytes possess a complete mechanism to synthesize the ECM components, and that thrombopoietin is a pivotal regulator of this new function inducing transforming growth factor-β1 (TGF-β1) release and consequent activation of the downstream pathways, both in vitro and in vivo. This activation results in a dose dependent increase of ECM component synthesis by megakaryocytes, which is reverted upon incubation with JAK and TGF-β1 receptor specific inhibitors. These data are pivotal for understanding the central role of megakaryocytes in creating their own regulatory niche within the bone marrow environment.

摘要

细胞外基质(ECM)成分引发维持骨髓内环境稳定所需的关键生化和生物力学信号。在我们的研究中,我们证明了一种主要由III型和IV型胶原蛋白以及纤连蛋白组成的细胞周基质包围着骨髓中的人类巨核细胞。我们收集的数据支持以下假设:骨髓巨核细胞拥有合成ECM成分的完整机制,并且血小板生成素是这一新功能的关键调节因子,它在体外和体内均可诱导转化生长因子-β1(TGF-β1)释放并随后激活下游通路。这种激活导致巨核细胞合成ECM成分的量呈剂量依赖性增加,而与JAK和TGF-β1受体特异性抑制剂孵育后这种增加会逆转。这些数据对于理解巨核细胞在骨髓环境中创建自身调节微环境的核心作用至关重要。

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