Adult articular cartilage has biomechanical, compositional, structural, and biological properties that can provide effective load-bearing function for decades. Developmental mechanisms create such mature articular cartilage, of a particular size and shape, through growth and remodeling of immature tissue under biochemical and biomechanical regulation. The fabrication of cartilaginous tissue grafts, of an analogously stable function and form, underlies a number of existing surgical treatments for restoring damaged joints as well as emerging tissue engineering therapies. The long-term goal of this project is to establish integrative scientific principles that allow the bioengineering fabrication of articular cartilage grafts of increasingly precise properties (maturity, size, shape), effective for surgical treatment of damaged diarthrodial joints. In the initial funding period, we established (1) the baseline mechanical and compositional properties of articular cartilage at various stages of growth, and their correlative relationships, (2) the ability of biological and biomechanical stimuli to modulate cell functions and in vitro growth during up to six weeks of culture, (3) the effects of targeted matrix manipulations on in vitro growth, implicating a critical role for matrix remodeling and in particular a balance between swelling mediated by fixed charge and restraint by the collagen network, and (4) methods to determine chondrocyte organization in three dimensions within cartilage tissue. These results evoked the current working hypothesis, that the maturity, size, and shape of live articular cartilage grafts can be prescribed by a combination of biological and biomechanical stimuli and chemical manipulations that modulate the remodeling of selected components of the tissue matrix. To test this hypothesis, studies are proposed to determine if in vitro remodeling of articular cartilage tissue can be manipulated to achieve (1) adult-like maturity, i.e., to undergo functional maturation of the load-bearing tissue matrix, (2) increased size, i.e., to undergo axial and radial expansion, and (3) desired shapes, i.e., to become convex or concave. Experiments will manipulate (a) matrix composition and assembly, (b) cell metabolism, and (c) the internal growth stress, and analyze kinematic growth. Relevance to Public Health. The proposed research will establish new scientific concepts and engineering methods to create a next generation of therapeutic cartilage tissue. The resultant tissue grafts would be especially useful for replacement of articular cartilage for large and advanced defects.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR044058-15
Application #
7902136
Study Section
Skeletal Biology Structure and Regeneration Study Section (SBSR)
Program Officer
Wang, Fei
Project Start
1996-04-01
Project End
2011-08-31
Budget Start
2010-09-01
Budget End
2011-08-31
Support Year
15
Fiscal Year
2010
Total Cost
$316,363
Indirect Cost
Name
University of California San Diego
Department
Engineering (All Types)
Type
Schools of Arts and Sciences
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Su, Alvin W; Chen, Yunchan; Dong, Yao et al. (2018) Biomechanics of osteochondral impact with cushioning and graft Insertion: Cartilage damage is correlated with delivered energy. J Biomech 73:127-136
Su, Alvin W; Chen, Yunchan; Wailes, Dustin H et al. (2018) Impact insertion of osteochondral grafts: Interference fit and central graft reduction affect biomechanics and cartilage damage. J Orthop Res 36:377-386
Caffrey, Jason P; Cory, Esther; Wong, Van W et al. (2016) Ex vivo loading of trussed implants for spine fusion induces heterogeneous strains consistent with homeostatic bone mechanobiology. J Biomech 49:4090-4097
Goodrich, Laurie R; Chen, Albert C; Werpy, Natasha M et al. (2016) Addition of Mesenchymal Stem Cells to Autologous Platelet-Enhanced Fibrin Scaffolds in Chondral Defects: Does It Enhance Repair? J Bone Joint Surg Am 98:23-34
Watson, Deborah; Reuther, Marsha S; Wong, Van W et al. (2016) Effect of hyaluronidase on tissue-engineered human septal cartilage. Laryngoscope 126:1984-9
Hollenstein, Jérôme; Terrier, Alexandre; Cory, Esther et al. (2015) Mechanical evaluation of a tissue-engineered zone of calcification in a bone-hydrogel osteochondral construct. Comput Methods Biomech Biomed Engin 18:332-7
Reuther, Marsha S; Briggs, Kristen K; Neuman, Monica K et al. (2014) Volume Expansion of Tissue Engineered Human Nasal Septal Cartilage. J Otol Rhinol 3:
Mologne, Timothy S; Cory, Esther; Hansen, Bradley C et al. (2014) Osteochondral allograft transplant to the medial femoral condyle using a medial or lateral femoral condyle allograft: is there a difference in graft sources? Am J Sports Med 42:2205-13
Kushnaryov, Anton; Yamaguchi, Tomonoro; Briggs, Kristen K et al. (2014) Evaluation of Autogenous Engineered Septal Cartilage Grafts in Rabbits- A Minimally Invasive Preclinical Model. Adv Otolaryngol 2014:415821
Twu, Chih-Wen; Reuther, Marsha S; Briggs, Kristen K et al. (2014) Effect of oxygen tension on tissue-engineered human nasal septal chondrocytes. Allergy Rhinol (Providence) 5:125-31

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