A magnetic resonance-compatible perfusion bioreactor system for three-dimensional human mesenchymal stem cell construct development

被引:11
作者
Crowe, Jason J. [2 ,3 ]
Grant, Samuel C. [1 ,2 ,3 ]
Logan, Timothy M. [1 ,3 ,4 ]
Ma, Teng [2 ,3 ]
机构
[1] Florida State Univ, Natl High Magnet Field Lab, Tallahassee, FL 32310 USA
[2] Florida State Univ, Dept Chem & Biomed Engn, Tallahassee, FL 32310 USA
[3] Florida State Univ, Inst Mol Biophys, Tallahassee, FL 32310 USA
[4] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32310 USA
关键词
Human mesenchymal stem cells; Nuclear magnetic resonance; Perfusion bioreactor; Microenvironment; 3D constructs; Tissue engineering; ENGINEERED MENISCAL CARTILAGE; KEY METABOLIC FUNCTIONS; IN-VIVO; NMR-SPECTROSCOPY; TISSUE; GROWTH; MICROSCOPY; CULTURE; VITRO;
D O I
10.1016/j.ces.2011.05.046
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Human mesenchymal stem cells (hMSCs) have significant potential for therapeutic tissue regeneration and repair. The creation of functional 3D constructs from hMSCs depends on the innate ability of MSCs to proliferate and differentiate, and is strongly influenced by the culture conditions. An inherent challenge in investigating 3D cellular construct development is the dynamic monitoring of the cellular and physiological environment over the course of construct formation. In this project, a novel 3D MR-compatible perfusion bioreactor using 3D poly(ethylene terephthalate) scaffolds was developed to provide such monitoring. The bioreactor system integrates cell seeding and growth, supports high density 3D tissue construct growth and facilitates repeated nuclear magnetic resonance (MR) signal acquisitions under both static and perfusion conditions. The reactor system also has the capacity to modulate macroscopic flow modes that simulates various tissue growth environments with repeated MR signal acquisition, providing the ability to gain insight into the dynamic interplay between the stem cells in the developing constructs and their microenvironment. Using H-1 MR spectroscopy and MR imaging, localized spectroscopic data as well as imaging-based T-2 and diffusion quantification were acquired from the hMSC growth construct for up to 40 days. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4138 / 4147
页数:10
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