4.8 Article

Molecular stiffness cues of an interpenetrating network hydrogel for cell adhesion

期刊

MATERIALS TODAY BIO
卷 15, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.mtbio.2022.100323

关键词

IPNs; Nanomechanics; Mechanotransduction; Cell adhesion; AFM

资金

  1. Alexander von Humboldt Foundation
  2. DFG [SFB1027]

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Studying cells' response to the macroscopic and nanoscale properties of biomaterials requires model systems with different length scales. IPN design can offer insights into cell adhesion and spreading behaviors, presenting different mechanical cues at the molecular scale but similar properties at the macroscopic length scale. Cells adhered to the IPN guest network with lower molecular stiffness exhibited distinct characteristics compared to those attached to the single network.
Understanding cells' response to the macroscopic and nanoscale properties of biomaterials requires studies in model systems with the possibility to tailor their mechanical properties and different length scales. Here, we describe an interpenetrating network (IPN) design based on a stiff PEGDA host network interlaced within a soft 4arm PEG-Maleimide/thiol (guest) network. We quantify the nano- and bulk mechanical behavior of the IPN and the single network hydrogels by single-molecule force spectroscopy and rheological measurements. The IPN presents different mechanical cues at the molecular scale, depending on which network is linked to the probe, but the same mechanical properties at the macroscopic length scale as the individual host network. Cells attached to the interpenetrating (guest) network of the IPN or to the single network (SN) PEGDA hydrogel modified with RGD adhesive ligands showed comparable attachment and spreading areas, but cells attached to the guest network of the IPN, with lower molecular stiffness, showed a larger number and size of focal adhesion complexes and a higher concentration of the Hippo pathway effector Yes-associated protein (YAP) than cells linked to the PEGDA single network. The observations indicate that cell adhesion to the IPN hydrogel through the network with lower molecular stiffness proceeds effectively as if a higher ligand density is offered. We claim that IPNs can be used to decipher how changes in ECM design and connectivity at the local scale affect the fate of cells cultured on biomaterials.

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