Guiding Stem Cell Tenogenesis by Modulation of Growth Factor Signaling and Cell‐Scale Biophysical Cues in Bioengineered Constructs

Author:

Teixeira Simão P. B.12ORCID,Pardo Alberto123ORCID,Bakht Syeda M.12ORCID,Gomez‐Florit Manuel124ORCID,Reis Rui L.12ORCID,Gomes Manuela E.12ORCID,Domingues Rui M. A.12ORCID

Affiliation:

1. 3B's Research Group I3Bs – Research Institute on Biomaterials Biodegradables and Biomimetics of University of Minho Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine AvePark – Parque de Ciência e Tecnologia, Zona Industrial da Gandra Barco GMR 4805‐017 Portugal

2. ICVS/3B's–PT Government Associate Laboratory Braga/Guimarães Portugal

3. Colloids and Polymers Physics Group Particle Physics Department and Materials Institute (iMATUS) University of Santiago de Compostela Santiago de Compostela 15782 Spain

4. Health Research Institute of the Balearic Islands (IdISBa) Palma 07010 Spain

Abstract

AbstractTendon injuries and tendinopathies are increasingly prevalent health problems currently lacking effective treatments. Tissue engineering offers promising strategies to boost the low innate regenerative ability of tendons. Within this context, the simultaneous leveraging of both physical and biochemical cues by engineered scaffolding systems can be explored to promote a stronger tenogenic response from stem cells. Here, molecularly imprinted polymeric nanoparticles (MINPs) against transforming growth factor (TGF)‐β3 are combined with bioinspired anisotropic hydrogels to produce tenogenesis‐inductive constructs. MINPs are first solid phase‐imprinted against a TGF‐β3 epitope, achieving an affinity comparable to monoclonal antibodies. MINPs and magnetically‐responsive microfibers are then encapsulated together with adipose‐derived stem cells within gelatin‐based hydrogels, applying a magnetostatic field during gelation to align the microfibers. The created anisotropic microstructure guides cell growth and elongation unidirectionally, while MINPs act as artificial receptors for TGF‐β3, potentiating its paracrine action in the cellular microenvironment. The combination of both stimuli proves effective at increasing TGF‐β signaling, which promotes the expression of tendon‐associated genes and corresponding protein synthesis, suggesting that microstructural cues and biomolecule sequestration act in tandem to direct cell fate commitment. Overall, this system recapitulates several elements of tendon development, constituting a promising strategy for the regeneration of this tissue.

Funder

European Social Fund

Instituto de Salud Carlos III

Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia

H2020 European Research Council

HORIZON EUROPE European Research Council

Fundação para a Ciência e a Tecnologia

Comissão de Coordenação e Desenvolvimento Regional do Norte

European Regional Development Fund

Publisher

Wiley

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