TY - JOUR
T1 - Materials-driven fibronectin assembly on nanoscale topography enhances mesenchymal stem cell adhesion, protecting cells from bacterial virulence factors and preventing biofilm formation
AU - Damiati, Laila A.
AU - Tsimbouri, Monica P.
AU - Hernandez, Virginia Llopis
AU - Jayawarna, Vineetha
AU - Ginty, Mark
AU - Childs, Peter
AU - Xiao, Yinbo
AU - Burgess, Karl
AU - Wells, Julia
AU - Sprott, Mark R.
AU - Meek, R. M.Dominic
AU - Li, Peifeng
AU - Oreffo, Richard O.C.
AU - Nobbs, Angela
AU - Ramage, Gordon
AU - Su, Bo
AU - Salmeron-Sanchez, Manuel
AU - Dalby, Matthew J.
N1 - Funding Information:
L.A.D. was supported by a scholarship from Jeddah University and the Saudi Arabian Government . The work was also supported by grants from EPSRC ( EP/K034898/1 ) and MRC ( MR/S010343/1 ). We thank Carol-Anne Smith and Marcus Eales for laboratory support and Margaret Mullin for help with microscopy.
Publisher Copyright:
© 2021
PY - 2022/1/1
Y1 - 2022/1/1
N2 - Post-operative infection is a major complication in patients recovering from orthopaedic surgery. As such, there is a clinical need to develop biomaterials for use in regenerative surgery that can promote mesenchymal stem cell (MSC) osteospecific differentiation and that can prevent infection caused by biofilm-forming pathogens. Nanotopographical approaches to pathogen control are being identified, including in orthopaedic materials such as titanium and its alloys. These topographies use high aspect ratio nanospikes or nanowires to prevent bacterial adhesion but these features also significantly reduce MSC adhesion and activity. Here, we use a poly (ethyl acrylate) (PEA) polymer coating on titanium nanowires to spontaneously organise fibronectin (FN) and to deliver bone morphogenetic protein 2 (BMP2) to enhance MSC adhesion and osteospecific signalling. Using a novel MSC–Pseudomonas aeruginosa co-culture, we show that the coated nanotopographies protect MSCs from cytotoxic quorum sensing and signalling molecules, enhance MSC adhesion and osteoblast differentiation and reduce biofilm formation. We conclude that the PEA polymer-coated nanotopography can both support MSCs and prevent pathogens from adhering to a biomaterial surface, thus protecting from biofilm formation and bacterial infection, and supporting osteogenic repair.
AB - Post-operative infection is a major complication in patients recovering from orthopaedic surgery. As such, there is a clinical need to develop biomaterials for use in regenerative surgery that can promote mesenchymal stem cell (MSC) osteospecific differentiation and that can prevent infection caused by biofilm-forming pathogens. Nanotopographical approaches to pathogen control are being identified, including in orthopaedic materials such as titanium and its alloys. These topographies use high aspect ratio nanospikes or nanowires to prevent bacterial adhesion but these features also significantly reduce MSC adhesion and activity. Here, we use a poly (ethyl acrylate) (PEA) polymer coating on titanium nanowires to spontaneously organise fibronectin (FN) and to deliver bone morphogenetic protein 2 (BMP2) to enhance MSC adhesion and osteospecific signalling. Using a novel MSC–Pseudomonas aeruginosa co-culture, we show that the coated nanotopographies protect MSCs from cytotoxic quorum sensing and signalling molecules, enhance MSC adhesion and osteoblast differentiation and reduce biofilm formation. We conclude that the PEA polymer-coated nanotopography can both support MSCs and prevent pathogens from adhering to a biomaterial surface, thus protecting from biofilm formation and bacterial infection, and supporting osteogenic repair.
KW - anti-bacterial
KW - mesenchymal stem cells
KW - multifunctional materials
KW - nanoscale coatings
KW - nanotopography
U2 - 10.1016/j.biomaterials.2021.121263
DO - 10.1016/j.biomaterials.2021.121263
M3 - Article
C2 - 34810036
AN - SCOPUS:85119420996
SN - 0142-9612
VL - 280
JO - Biomaterials
JF - Biomaterials
M1 - 121263
ER -