

Hydrogels are widely used as provisional matrices for tissue engineering and regenerative medicine, showing also great promise as platforms for 3D cell culture. Different bio-functionalization strategies have been proposed to enhance the biological performance of hydrogels, particularly when they lack intrinsic bioactivity. In this context, the design of artificial materials that mimic structural and functional features of the natural extracellular matrix (ECM) has been pursued. This review presents an overview on bioengineering approaches of integrating protease-sensitive motifs into hydrogels, for the creation of cell-responsive biomimetic scaffolding materials that degrade in response to their proteolytic microenvironment. The successful incorporation of protease-sensitive motifs in several synthetic and natural polymers, which has been achieved using various chemical routes, is described. In each case, the selected peptide sequences and their target proteases are highlighted, along with the main achievements of the study. A critical analysis of current limitations and recent advances is also provided, along with suggestions for further improvements. © 2014 Elsevier Ltd.
| Engineering controlled terms: | Biomimetic materialsBiomimeticsCell cultureEnzyme activityHydrogelsScaffolds (biology) |
|---|---|
| Engineering uncontrolled terms | Artificial materialBiofunctionalizationBiological performanceEnzymatic cleavageExtracellular matricesProtease sensitiveProteolytic degradationScaffolding materials |
| Engineering main heading: | Cell engineering |
| Funding sponsor | Funding number | Acronym |
|---|---|---|
| Programa Operacional Temático Factores de Competitividade | ||
| Programa Operacional Temático Factores de Competitividade | ||
| Fundação para a Ciência e a Tecnologia See opportunities | FCOMP-01-0124-FEDER-010915,Pest-C/SAU/LA0002/2013,PTDC/SAU-BEB/101235/2008 | |
| Fundação para a Ciência e a Tecnologia See opportunities |
This work was financed by FEDER funds through the Programa Operacional Factores de Competitividade–COMPETE) and by Portuguese funds through FCT —Fundação para a Ciência e a Tecnologia, in the framework of the projects Pest-C/SAU/LA0002/2013 and BIOMATRIX (PTDC/SAU-BEB/101235/2008 and FCOMP-01-0124-FEDER-010915). CB and KF acknowledge, respectively, FCT Investigator program and CAPES “Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (BEX 5559-10-3)”. The authors are grateful to Anabela Nunes (Office for Science Communication of IBMC.INEB) for the image design. The funding source(s) had neither involvement in the collection, analysis and interpretation of data, in the writing of the report, nor in the decision to submit the article for publication.
Barrias, C.C.; INEB - Instituto de Engenharia Biomédica, Universidade Do Porto, Porto, Portugal
© Copyright 2018 Elsevier B.V., All rights reserved.