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

Author:

Abbonante Vittorio12,Di Buduo Christian A.12,Gruppi Cristian12,Malara Alessandro12,Gianelli Umberto3,Celesti Giuseppe4,Anselmo Achille4,Laghi Luigi4,Vercellino Marco56,Visai Livia56,Iurlo Alessandra7,Moratti Remigio2,Barosi Giovanni2,Rosti Vittorio2,Balduini Alessandra128

Affiliation:

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

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

3. Hematopathology Service, Division of Pathology, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy

4. Laboratory of Molecular Gastroenterology, Humanitas Clinical and Research Center, Rozzano, Milan, Italy

5. Center for Tissue Engineering (CIT), INSTM UdR of Pavia, University of Pavia, Pavia, Italy

6. Department of Occupational Medicine, Ergonomics and Disability, Salvatore Maugeri Foundation (FSM), Laboratory of Nanotechnology, Pavia, Italy

7. Oncohematology of the Elderly Unit, Oncohematology Division, IRCCS Ca' Granda–Maggiore Policlinico Hospital Foundation, Milan, Italy

8. Department of Biomedical Engineering, Tufts University, Medford, Massachusetts, USA

Abstract

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.

Funder

Cariplo Foundation

US National Institutes of Health

Italian Ministry of Health

Italian Ministry of University and Research, FIRB

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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