4.8 Review

Biomaterials for Sequestration of Growth Factors and Modulation of Cell Behavior

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 30, Issue 44, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201909011

Keywords

affinity binding; biomaterials; growth factors; molecular recognition; stem cells

Funding

  1. Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF) [NORTE-01-0145-FEDER-000021]
  2. European Union Framework Programme for Research and Innovation HORIZON 2020, under the TEAMING Grant [739572]
  3. Twinning Grant [810850-Achilles]
  4. European Research Council [772817]
  5. FCT/MCTES (Fundacao para a Ciencia e a Tecnologia/Ministerio da Ciencia, Tecnologia, e Ensino Superior)
  6. Fundo Social Europeu atraves do Programa Operacional do Capital Humano (FSE/POCH) [PD/169/2013-PD/BD/143039/2018, PTDC/NAN-MAT/30595/2017]
  7. Fundação para a Ciência e a Tecnologia [PTDC/NAN-MAT/30595/2017] Funding Source: FCT

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Growth factors (GFs) are proteins secreted by cells that regulate a variety of biological processes. Although they have long been proposed as potent therapeutic agents, their administration in a soluble form has proven costly and ineffective due to their short half-lives in biological environments. Biomaterial-based approaches are increasingly sought as alternatives to improve the efficacy or, ideally, replace the need for exogenous administration of GFs in regenerative medicine strategies. The means by which these systems evolve from biomaterials for conventional controlled release of GFs to the recent extracellular matrix (ECM)-inspired approaches for sequestering these labile molecules and regulating their spatiotemporal activity and presentation are reviewed. Focus is placed on biomaterials functionalized either with ECM components, which show promiscuous GF binding, or with targeted GF ligands (antibodies, aptamers, or peptides). The potential of synthetic platforms with abiotic affinity as cost-effective alternatives to the current biological ligands is also discussed. Overall, the various GF sequestering systems developed so far have remarkably improved the activity of GFs at reduced doses and, in some cases, completely avoided the need for their exogenous administration to guide cell fates. These bioinspired concepts thus enable the rational exploration of the full therapeutic potential of GFs in regenerative medicine.

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