| Literature DB >> 26895780 |
Adam B Nover1, Brian K Jones2, William T Yu3, Daniel S Donovan4, Jeremy D Podolnick5, James L Cook6, Gerard A Ateshian7, Clark T Hung8.
Abstract
Engineering of large articular cartilage tissue constructs remains a challenge as tissue growth is limited by nutrient diffusion. Here, a novel strategy is investigated, generating large constructs through the assembly of individually cultured, interlocking, smaller puzzle-shaped subunits. These constructs can be engineered consistently with more desirable mechanical and biochemical properties than larger constructs (~4-fold greater Young׳s modulus). A failure testing technique was developed to evaluate the physiologic functionality of constructs, which were cultured as individual subunits for 28 days, then assembled and cultured for an additional 21-35 days. Assembled puzzle constructs withstood large deformations (40-50% compressive strain) prior to failure. Their ability to withstand physiologic loads may be enhanced by increases in subunit strength and assembled culture time. A nude mouse model was utilized to show biocompatibility and fusion of assembled puzzle pieces in vivo. Overall, the technique offers a novel, effective approach to scaling up engineered tissues and may be combined with other techniques and/or applied to the engineering of other tissues. Future studies will aim to optimize this system in an effort to engineer and integrate robust subunits to fill large defects.Entities:
Keywords: Articular cartilage; Nutrient limitations; Puzzle; Scaling up; Tissue engineering
Mesh:
Year: 2016 PMID: 26895780 PMCID: PMC4907770 DOI: 10.1016/j.jbiomech.2016.01.023
Source DB: PubMed Journal: J Biomech ISSN: 0021-9290 Impact factor: 2.712