诺金
骨形态发生蛋白2
细胞生物学
骨形态发生蛋白
体内
化学
祖细胞
脚手架
体外
生物医学工程
干细胞
生物
生物化学
医学
基因
生物技术
作者
Gregory M. Cooper,Eric D. Miller,Gary E. DeCesare,Arvydas Ūsas,Emily L. Lensie,Michael R. Bykowski,Johnny Huard,Lee E. Weiss,Joseph E. Losee,Phil G. Campbell
出处
期刊:Tissue Engineering Part A
[Mary Ann Liebert, Inc.]
日期:2009-12-22
卷期号:16 (5): 1749-1759
被引量:125
标识
DOI:10.1089/ten.tea.2009.0650
摘要
The purpose of this study was to demonstrate spatial control of osteoblast differentiation in vitro and bone formation in vivo using inkjet bioprinting technology and to create three-dimensional persistent bio-ink patterns of bone morphogenetic protein-2 (BMP-2) and its modifiers immobilized within microporous scaffolds. Semicircular patterns of BMP-2 were printed within circular DermaMatrix human allograft scaffold constructs. The contralateral halves of the constructs were unprinted or printed with BMP-2 modifiers, including the BMP-2 inhibitor, noggin. Printed bio-ink pattern retention was validated using fluorescent or (125)I-labeled bio-inks. Mouse C2C12 progenitor cells cultured on patterned constructs differentiated in a dose-dependent fashion toward an osteoblastic fate in register to BMP-2 patterns. The fidelity of spatial restriction of osteoblastic differentiation at the boundary between neighboring BMP-2 and noggin patterns improved in comparison with patterns without noggin. Acellular DermaMatrix constructs similarly patterned with BMP-2 and noggin were then implanted into a mouse calvarial defect model. Patterns of bone formation in vivo were comparable with patterned responses of osteoblastic differentiation in vitro. These results demonstrate that three-dimensional biopatterning of a growth factor and growth factor modifier within a construct can direct cell differentiation in vitro and tissue formation in vivo in register to printed patterns.
科研通智能强力驱动
Strongly Powered by AbleSci AI