Tissue engineered humanized bone supports human hematopoiesis in vivo

被引:59
作者
Holzapfel, Boris M. [1 ,2 ]
Hutmacher, Dietmar W. [1 ,3 ,4 ]
Nowlan, Bianca [5 ,6 ]
Barbier, Valerie [5 ,6 ]
Thibaudeau, Laure [1 ]
Theodoropoulos, Christina [1 ]
Hooper, John D. [7 ]
Loessner, Daniela [1 ]
Clements, Judith A. [7 ]
Russell, Pamela J. [7 ,8 ]
Pettit, Allison R. [9 ]
Winkler, Ingrid G. [5 ,6 ]
Levesque, Jean-Pierre [5 ,6 ,10 ]
机构
[1] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Regenerat Med Grp, Brisbane, Qld 4049, Australia
[2] Univ Wurzburg, Orthoped Ctr Musculoskeletal Res, D-97074 Wurzburg, Germany
[3] Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
[4] Tech Univ Munich, Inst Adv Study, D-85748 Munich, Germany
[5] Univ Queensland, Stem Cell Biol Grp, Translat Res Inst, Brisbane, Qld 4102, Australia
[6] Univ Queensland, Stem Cells & Canc Grp, Translat Res Inst, Blood & Bone Dis Program,Mater Res Inst, Brisbane, Qld 4102, Australia
[7] Australian Prostate Canc Res Ctr Queensland, Translat Res Inst, Brisbane, Qld 4102, Australia
[8] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Cells & Tissue Domain, Brisbane, Qld 4049, Australia
[9] Univ Queensland, Mater Res Inst, Blood & Bone Dis Program, Translat Res Inst,Bones & Immunol Grp, Brisbane, Qld 4102, Australia
[10] Univ Queensland, Sch Med, Brisbane, Qld 4006, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
Tissue Engineering; Humanized niche; Bone organ; Hematopoietic stem cells; Engraftment; Transplantation; STEM-CELL NICHE; MARROW STROMAL FIBROBLASTS; CANCER METASTASIS; MECHANISMS; INSIGHTS; MICROENVIRONMENTS; OPPORTUNITIES; ENVIRONMENT; MODELS;
D O I
10.1016/j.biomaterials.2015.04.057
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Advances in tissue-engineering have resulted in a versatile tool-box to specifically design a tailored microenvironment for hematopoietic stem cells (HSCs) in order to study diseases that develop within this setting. However, most current in vivo models fail to recapitulate the biological processes seen in humans. Here we describe a highly reproducible method to engineer humanized bone constructs that are able to recapitulate the morphological features and biological functions of the HSC niches. Ectopic implantation of biodegradable composite scaffolds cultured for 4 weeks with human mesenchymal progenitor cells and loaded with rhBMP-7 resulted in the development of a chimeric bone organ including a large number of human mesenchymal cells which were shown to be metabolically active and capable of establishing a humanized microenvironment supportive of the homing and maintenance of human HSCs. A syngeneic mouse-to-mouse transplantation assay was used to prove the functionality of the tissue-engineered ossicles. We predict that the ability to tissue engineer a morphologically intact and functional large-volume bone organ with a humanized bone marrow compartment will help to further elucidate physiological or pathological interactions between human HSCs and their native niches. Crown Copyright (C) 2015 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:103 / 114
页数:12
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