Multipotent adult progenitor cell-loaded demineralized bone matrix for bone tissue engineering

被引:5
|
作者
Supronowicz, Peter [1 ]
Gill, Elise [1 ]
Trujillo, Angelica [1 ]
Thula, Taili [1 ]
Zhukauskas, Rasa [2 ]
Perry, Robert [3 ]
Cobb, Ronald R. [1 ]
机构
[1] RTI Biol, Biotechnol Dev Dept, Alachua, FL USA
[2] RTI Biol, Sports Med Grp, Alachua, FL USA
[3] Athersys Inc, Cleveland, OH USA
关键词
multipotent adult progenitor cells; tissue engineering; mineralization; bone; MARROW STROMAL CELLS; OSTEOBLAST DIFFERENTIATION; IN-VITRO; CORALLINE HYDROXYAPATITE; ISCHEMIC-INJURY; SPINAL-FUSION; ILIAC CREST; DONOR SITE; IMPLANTS; GRAFTS;
D O I
10.1002/term.1706
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Multipotent adult progenitor cells (MAPCs) from bone marrow have been shown to be capable of forming bone, cartilage and other connective tissues. In addition, MAPCs differentiate into lineages that are different from their germ layers of origin. Previous studies showed the ability of MAPCs to improve cardiac function and control allogenic-reactive responses associated with acute graft versus host disease. In the current study, we evaluated the ability of MAPCs to produce bone matrix on demineralized bone allograft substrates. Specifically, MAPCs expressed alkaline phosphatase, produced extracellular matrix proteins and deposited calcium-containing mineral on demineralized bone matrices. Furthermore, the addition of MAPCs on demineralized bone matrix (DBM) scaffolds enhanced osteoinductivity of the carrier in a rat ectopic pouch model. These results demonstrated the potential of MAPCs as a new approach for bone repair in tissue-engineering applications. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:275 / 283
页数:9
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