The successful construction of engineered tissues requires the re-creation of a biologically active extracellular environment in which to develop the product. Ultrasound therapy is currently used clinically to promote bone healing and has been shown to enhance soft tissue repair. Some biological effects of ultrasound are known to result from the mechanical forces associated with acoustic wave propagation. In vitro studies demonstrate that mechanical stresses positively affect both extracellular matrix (ECM) organization and cell behavior. Thus, we hypothesize that acoustically-driven mechanical forces can be used to control ECM deposition and promote cell and tissue function. In this proposal, we combine our knowledge of ECM biology and biomedical ultrasound to develop ultrasound-based enabling technologies for the fabrication and monitoring of functional 3D ECM and tissue analogs. To accomplish this goal, we have developed four specific aims.
In Aim 1, we will use ultrasound fields to fabricate ECM FN and collagen analogs, and optimize ultrasound exposure conditions that enhance ECM-mediated fibroblast and epithelial cell growth.
In Aim 2, we will develop the use of acoustically-driven mechanical forces to promote fibroblast migration into 3D, collagen- based tissue constructs.
In Aim 3, we will use acoustic fields to stimulate ECM organization in order to engineer the biological and material properties of collagen-based tissue constructs.
In Aim 4, we will apply and extend our experience in ultrasound tissue characterization technologies to non-destructively quantify mechanical and biological properties of engineered tissues in real-time. We envision immense potential for the use of ultrasound technologies to provide break-through technologies for tissue fabrication and monitoring. Furthermore, the ability of ultrasound to propagate through tissue as a focused beam has the potential to provide a revolutionary approach to locally regulate and monitor tissue regeneration deep within the body. Tissue engineering is a potentially revolutionary approach for replacing or regenerating diseased or destroyed organs and tissues. The current lack of available tissue analogs reflects an inability to create 3-D scaffolds that have both biological activity and adequate mechanical strength. We will develop ultrasound- based enabling technologies with the dual capacity to (i) create biologically-active, 3-D tissue constructs for tissue engineering and (ii) non-invasively monitor the biological and mechanical properties of these constructs.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB008368-04
Application #
7880016
Study Section
Special Emphasis Panel (ZHL1-CSR-N (O1))
Program Officer
Hunziker, Rosemarie
Project Start
2007-09-24
Project End
2012-12-31
Budget Start
2010-07-01
Budget End
2012-12-31
Support Year
4
Fiscal Year
2010
Total Cost
$498,445
Indirect Cost
Name
University of Rochester
Department
Pharmacology
Type
Schools of Dentistry
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627
Mercado, Karla P; Helguera, MarĂ­a; Hocking, Denise C et al. (2014) Estimating cell concentration in three-dimensional engineered tissues using high frequency quantitative ultrasound. Ann Biomed Eng 42:1292-304
Gildner, Candace D; Roy, Daniel C; Farrar, Christopher S et al. (2014) Opposing effects of collagen I and vitronectin on fibronectin fibril structure and function. Matrix Biol 34:33-45
Garvin, Kelley A; Dalecki, Diane; Yousefhussien, Mohammed et al. (2013) Spatial patterning of endothelial cells and vascular network formation using ultrasound standing wave fields. J Acoust Soc Am 134:1483-90
Garvin, Kelley A; VanderBurgh, Jacob; Hocking, Denise C et al. (2013) Controlling collagen fiber microstructure in three-dimensional hydrogels using ultrasound. J Acoust Soc Am 134:1491-502
Sevilla, Carlos A; Dalecki, Diane; Hocking, Denise C (2013) Regional fibronectin and collagen fibril co-assembly directs cell proliferation and microtissue morphology. PLoS One 8:e77316
Lefort, Craig T; Wojciechowski, Katherine; Hocking, Denise C (2011) N-cadherin cell-cell adhesion complexes are regulated by fibronectin matrix assembly. J Biol Chem 286:3149-60
Garvin, Kelley A; Dalecki, Diane; Hocking, Denise C (2011) Vascularization of three-dimensional collagen hydrogels using ultrasound standing wave fields. Ultrasound Med Biol 37:1853-64
Carstensen, Edwin; Gracewski, Sheryl M; Dalecki, Diane (2011) Shear strain from irrotational tissue displacements near bubbles. J Acoust Soc Am 130:3467-71
McAleavey, Stephen (2011) Ultrasonic backscatter imaging by shear-wave-induced echo phase encoding of target locations. IEEE Trans Ultrason Ferroelectr Freq Control 58:102-11
Garvin, Kelley A; Hocking, Denise C; Dalecki, Diane (2010) Controlling the spatial organization of cells and extracellular matrix proteins in engineered tissues using ultrasound standing wave fields. Ultrasound Med Biol 36:1919-32

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