TY - JOUR
T1 - Programmable 3D silk bone marrow niche for platelet generation ex vivo and modeling of megakaryopoiesis pathologies
AU - Di Buduo, Christian A.
AU - Wray, Lindsay S.
AU - Tozzi, Lorenzo
AU - Malara, Alessandro
AU - Chen, Ying
AU - Ghezzi, Chiara E.
AU - Smoot, Daniel
AU - Sfara, Carla
AU - Antonelli, Antonella
AU - Spedden, Elise
AU - Bruni, Giovanna
AU - Staii, Cristian
AU - De Marco, Luigi
AU - Magnani, Mauro
AU - Kaplan, David L.
AU - Balduini, Alessandra
PY - 2015/4/2
Y1 - 2015/4/2
N2 - Wepresent a programmable bioengineered 3-dimensional silk-based bone marrow niche tissue system that successfully mimics the physiology of human bone marrow environment allowing us to manufacture functional human platelets ex vivo. Using stem/progenitor cells, megakaryocyte function and platelet generation were recorded in response to variations in extracellular matrix components, surface topography, stiffness, coculture with endothelial cells, and shear forces. Millions of human platelets were produced and showed to be functional based on multiple activation tests. Using adult hematopoietic progenitor cells our system demonstrated the ability to reproduce key steps of thrombopoiesis, including alterations observed in diseased states. A critical feature of the system is the use of natural silk protein biomaterial allowing us to leverage its biocompatibility, nonthrombogenic features, programmable mechanical properties, and surface binding of cytokines, extracellular matrix components, and endothelial-derived proteins. This in turn offers new opportunities for the study of blood component production ex vivo and provides a superior tissue system for the study of pathologic mechanisms of human platelet production.
AB - Wepresent a programmable bioengineered 3-dimensional silk-based bone marrow niche tissue system that successfully mimics the physiology of human bone marrow environment allowing us to manufacture functional human platelets ex vivo. Using stem/progenitor cells, megakaryocyte function and platelet generation were recorded in response to variations in extracellular matrix components, surface topography, stiffness, coculture with endothelial cells, and shear forces. Millions of human platelets were produced and showed to be functional based on multiple activation tests. Using adult hematopoietic progenitor cells our system demonstrated the ability to reproduce key steps of thrombopoiesis, including alterations observed in diseased states. A critical feature of the system is the use of natural silk protein biomaterial allowing us to leverage its biocompatibility, nonthrombogenic features, programmable mechanical properties, and surface binding of cytokines, extracellular matrix components, and endothelial-derived proteins. This in turn offers new opportunities for the study of blood component production ex vivo and provides a superior tissue system for the study of pathologic mechanisms of human platelet production.
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U2 - 10.1182/blood-2014-08-595561
DO - 10.1182/blood-2014-08-595561
M3 - Article
C2 - 25575540
AN - SCOPUS:84926616230
VL - 125
SP - 2254
EP - 2264
JO - Blood
JF - Blood
SN - 0006-4971
IS - 14
ER -