Literature DB >> 27995768

Substrate Stress-Relaxation Regulates Scaffold Remodeling and Bone Formation In Vivo.

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.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  biomaterials; bone regeneration; mechanotransduction; stress relaxation; tissue engineering

Mesh:

Substances:

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


  29 in total

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7.  Harnessing traction-mediated manipulation of the cell/matrix interface to control stem-cell fate.

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  27 in total

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9.  RNA-seq reveals diverse effects of substrate stiffness on mesenchymal stem cells.

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