Less is more: New biomimetic approach to control spatial and temporal cell loading for tissue engineering. Issue 11 (28th January 2014)
- Record Type:
- Journal Article
- Title:
- Less is more: New biomimetic approach to control spatial and temporal cell loading for tissue engineering. Issue 11 (28th January 2014)
- Main Title:
- Less is more: New biomimetic approach to control spatial and temporal cell loading for tissue engineering
- Authors:
- Deng, Dan
Liu, Wei
Cheema, Umber
Mudera, Vivek
Hadjipanayi, Ektoras
Brown, Robert A. - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <p>It is increasingly recognized that use of stiff biodegradable polymers in connective tissue engineering has an inherent flaw. Although polymer stiffness has early benefit for mechanical strength of implants, such pseudoprosthetic material function inevitably stress shields embedded cells, switching off their synthetic/remodeling functions. This core conundrum represents a tension between early mechanical benefits of polymer stiffness against blocking of cell load‐dependent matrix production. In effect, an ideal system would produce a gradual, transfer of load onto resident cells and their matrix. Toward this target, our "less is more" (LiM) hypothesis proposes that less stress shielding (polymer stiffness) will lead to more cell‐dependent tissue formation. To test this we have designed a hybrid segregation solution in which the cells are segregated into a native (but weak) collagen–gel matrix while the external mechanical loading is taken by temporary, reinforcing polyglycolic acid (PGA) fibers, with gradual, load transfer as the polymer µ‐fibers fracture. Dermal fibroblasts grew predictably in the hybrid construct and the fine, parallel PGA fibers fractured and fragmented due to hydrolysis, giving a fall of construct stiffness to near collagen‐only levels, over 14 days. The same fiber fracture and fall in stiffness occurred over 14 days in constructs implanted <italic>in vivo</italic>. In this case a cell dependent,<abstract abstract-type="main"> <title>Abstract</title> <p>It is increasingly recognized that use of stiff biodegradable polymers in connective tissue engineering has an inherent flaw. Although polymer stiffness has early benefit for mechanical strength of implants, such pseudoprosthetic material function inevitably stress shields embedded cells, switching off their synthetic/remodeling functions. This core conundrum represents a tension between early mechanical benefits of polymer stiffness against blocking of cell load‐dependent matrix production. In effect, an ideal system would produce a gradual, transfer of load onto resident cells and their matrix. Toward this target, our "less is more" (LiM) hypothesis proposes that less stress shielding (polymer stiffness) will lead to more cell‐dependent tissue formation. To test this we have designed a hybrid segregation solution in which the cells are segregated into a native (but weak) collagen–gel matrix while the external mechanical loading is taken by temporary, reinforcing polyglycolic acid (PGA) fibers, with gradual, load transfer as the polymer µ‐fibers fracture. Dermal fibroblasts grew predictably in the hybrid construct and the fine, parallel PGA fibers fractured and fragmented due to hydrolysis, giving a fall of construct stiffness to near collagen‐only levels, over 14 days. The same fiber fracture and fall in stiffness occurred over 14 days in constructs implanted <italic>in vivo</italic>. In this case a cell dependent, net enhancement of connective tissue stiffness could be identified in hybrid constructs, supporting the LiM hypothesis for cytomechanical control of matrix. This is the first demonstration of spatiotemporal load transfer as a customizable tool for improved, biomimetic connective tissue engineering. © 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 102A: 4108–4117, 2014.</p> </abstract> … (more)
- Is Part Of:
- Journal of biomedical materials research. Volume 102:Issue 11(2014)
- Journal:
- Journal of biomedical materials research
- Issue:
- Volume 102:Issue 11(2014)
- Issue Display:
- Volume 102, Issue 11 (2014)
- Year:
- 2014
- Volume:
- 102
- Issue:
- 11
- Issue Sort Value:
- 2014-0102-0011-0000
- Page Start:
- 4108
- Page End:
- 4117
- Publication Date:
- 2014-01-28
- Subjects:
- Biomedical materials -- Periodicals
610.28 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1552-4965 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jbm.a.35085 ↗
- Languages:
- English
- ISSNs:
- 1549-3296
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4953.720000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4218.xml