Tissue engineering and regenerative medicine (TE/RM) is an evolving interdisciplinary field that integrates engineering with biology and medicine for the development of functional tissues and organs. Monitoring of tissues in vitro prior to implantation and assessment of tissues in vivo during development are both essential in order to optimize the regeneration of tissue and the restoration of organ function. Since direct visualization of developing tissues, i.e., tissue sampling via sacrifice or biopsy, is invasive and wasteful, one challenge in TE/RM is establishing non-invasive tools to monitor the development of the constructs in vitro and in vivo. In addition, visualization of the transitional region between the tissue implant and the surrounding tissues is critical to the establishment of the overall success of the procedure. MRI is increasingly being used in TE/RM to monitor the remodeling and regeneration of engineered tissues. Bioengineers can now generate spatial maps of MR relaxation times, diffusion coefficients, magnetization transfer ratios, and the shear modulus to monitor, for example, new bone growth for prosthetic therapy in TE/RM. We hypothesize that MR can be extended to monitor quantitatively the growth of engineered tissues including bone, fat, and cartilage. By its periodic application in vitro and in vivo MR can enable the much anticipated successes in TE/RM. Our preliminary data demonstrate that quantitative MR methods can be applied to characterize non-invasively the changes associated with adipogenesis, osteogenesis, and chondrogenesis in tissue-engineered MSC-based constructs. This in vitro work established that MR acquired data can be directly correlated with the underlying tissue composition and structure as measured by biochemical and histological techniques. Our long term goal is to extend these methods to assess the structure and function of developing, engineered tissues in vivo. In order to achieve this goal we have assembled an interdisciplinary team of imaging scientists, tissue engineers and clinicians. The proposed work forms a 5-year plan to establish useful clinical MR tools for the optimization of TE/RM specifically for chondrogenic tissues. Public Health Relevance Statement (provided by applicant): The objective of this study is to develop new techniques for monitoring engineered chondrogenic tissues using magnetic resonance imaging and magnetic resonance elastography. Magnetic resonance imaging provides three dimensional views of developing tissue at all stages of growth without the need to sacrifice the animal or to biopsy the tissue. Magnetic resonance elastography gives a direct measure of the strength and stiffness of regenerating tissue: critical information needed to guide the design of new methods of tissue engineering and to assess the success of tissue implants for restoring tissue damaged by disease, injury or cancer treatment.

Public Health Relevance

The objective of this study is to develop new techniques for monitoring engineered chondrogenic tissues using magnetic resonance imaging and magnetic resonance elastography. Magnetic resonance imaging provides three dimensional views of developing tissue at all stages of growth without the need to sacrifice the animal or to biopsy the tissue. Magnetic resonance elastography gives a direct measure of the strength and stiffness of regenerating tissue: critical information needed to guide the design of new methods of tissue engineering and to assess the success of tissue implants for restoring tissue damaged by disease, injury or cancer treatment.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
3R01EB007537-02S1
Application #
8122856
Study Section
Special Emphasis Panel (ZEB1-OSR-D (J1))
Program Officer
Hunziker, Rosemarie
Project Start
2009-05-01
Project End
2013-02-28
Budget Start
2010-03-01
Budget End
2011-02-28
Support Year
2
Fiscal Year
2010
Total Cost
$103,188
Indirect Cost
Name
University of Illinois at Chicago
Department
Biomedical Engineering
Type
Schools of Engineering
DUNS #
098987217
City
Chicago
State
IL
Country
United States
Zip Code
60612
Magin, Richard L; Karaman, M Muge; Hall, Matt G et al. (2018) Capturing complexity of the diffusion-weighted MR signal decay. Magn Reson Imaging :
Schwartz, Benjamin L; Yin, Ziying; Magin, Richard L (2016) Mechanical analysis of an axially symmetric cylindrical phantom with a spherical heterogeneity for MR elastography. Phys Med Biol 61:6821-6832
Reiter, David A; Magin, Richard L; Li, Weiguo et al. (2016) Anomalous T2 relaxation in normal and degraded cartilage. Magn Reson Med 76:953-62
Duan, Bin; Yin, Ziying; Hockaday Kang, Laura et al. (2016) Active tissue stiffness modulation controls valve interstitial cell phenotype and osteogenic potential in 3D culture. Acta Biomater 36:42-54
Schwartz, Benjamin L; Yin, Ziying; Yasar, Temel K et al. (2016) Scattering and Diffraction of Elastodynamic Waves in a Concentric Cylindrical Phantom for MR Elastography. IEEE Trans Biomed Eng 63:2308-2316
Majumdar, Shreyan; Pothirajan, Padmabharathi; Dorcemus, Deborah et al. (2016) High Field Sodium MRI Assessment of Stem Cell Chondrogenesis in a Tissue-Engineered Matrix. Ann Biomed Eng 44:1120-7
Klatt, Dieter; Johnson, Curtis L; Magin, Richard L (2015) Simultaneous, multidirectional acquisition of displacement fields in magnetic resonance elastography of the in vivo human brain. J Magn Reson Imaging 42:297-304
Ravindran, Sriram; Kotecha, Mrignayani; Huang, Chun-Chieh et al. (2015) Biological and MRI characterization of biomimetic ECM scaffolds for cartilage tissue regeneration. Biomaterials 71:58-70
Wang, Vincent M; Karas, Vasili; Lee, Andrew S et al. (2015) Assessment of glenoid chondral healing: comparison of microfracture to autologous matrix-induced chondrogenesis in a novel rabbit shoulder model. J Shoulder Elbow Surg 24:1789-800
Ye, Allen Q; Hubbard Cristinacce, Penny L; Zhou, Feng-Lei et al. (2014) Diffusion tensor MRI phantom exhibits anomalous diffusion. Conf Proc IEEE Eng Med Biol Soc 2014:746-9

Showing the most recent 10 out of 33 publications