| Literature DB >> 27995768 |
Max Darnell1,2, Simon Young1,2, Luo Gu1,2, Nisarg Shah1,2, Evi Lippens3,4, James Weaver2, Georg Duda2,3,4, David Mooney1,2.
Abstract
The rate of stress relaxation of adhesion substrates potently regulates cell fate and function in vitro, and in this study the authors test whether it can regulate bone formation in vivo by implanting alginate gels with differing rates of stress-relaxation carrying human mesenchymal stem cells into rat calvarial defects. After three months, the rats that received fast-relaxing hydrogels (t1/2 ≈ 50 s) show significantly more new bone growth than those that received slow-relaxing, stiffness-matched hydrogels. Strikingly, substantial bone regeneration results from rapidly relaxing hydrogels even in the absence of transplanted cells. Histological analysis reveals that the new bone formed with rapidly relaxing hydrogels is mature and accompanied by extensive matrix remodeling and hydrogel disappearance. This tissue invasion is found to be prominent after just two weeks and the ability of stress relaxation to modulate cell invasion is confirmed with in vitro analysis. These results suggest that substrate stress relaxation can mediate scaffold remodeling and thus tissue formation, giving tissue engineers a new parameter for optimizing bone regeneration.Entities:
Keywords: biomaterials; bone regeneration; mechanotransduction; stress relaxation; tissue engineering
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Year: 2016 PMID: 27995768 PMCID: PMC5440842 DOI: 10.1002/adhm.201601185
Source DB: PubMed Journal: Adv Healthc Mater ISSN: 2192-2640 Impact factor: 9.933