dc.contributor.author | Simpson, Fiona | |
dc.contributor.author | McTiernan, Christopher D. | |
dc.contributor.author | Mirazul Islam, Mohammad | |
dc.contributor.author | Buznyk, Oleksiy | |
dc.contributor.author | Lewis, Philip N. | |
dc.contributor.author | Meek, Keith M. | |
dc.contributor.author | Haagdorens, Michel | |
dc.contributor.author | Audiger, Cindy | |
dc.contributor.author | Lesage, Sylvie | |
dc.contributor.author | Gueriot, François-Xavier | |
dc.contributor.author | Brunette, Isabelle | |
dc.contributor.author | Robert, Marie-Claude | |
dc.contributor.author | Olsen, David | |
dc.contributor.author | Koivusalo, Laura | |
dc.contributor.author | Liszka, Aneta | |
dc.contributor.author | Fagerholm, Per | |
dc.contributor.author | Gonzalez-Andrades, Miguel | |
dc.contributor.author | Griffith, May | |
dc.date.accessioned | 2023-01-24T17:34:52Z | |
dc.date.available | NO_RESTRICTION | fr |
dc.date.available | 2023-01-24T17:34:52Z | |
dc.date.issued | 2021-05-21 | |
dc.identifier.uri | http://hdl.handle.net/1866/27344 | |
dc.publisher | Nature Research | fr |
dc.rights | Ce document est mis à disposition selon les termes de la Licence Creative Commons Paternité 4.0 International. / This work is licensed under a Creative Commons Attribution 4.0 International License. | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/deed.fr | |
dc.subject | Implants | fr |
dc.subject | Translational research | fr |
dc.title | Collagen analogs with phosphorylcholine are inflammation-suppressing scaffolds for corneal regeneration from alkali burns in mini-pigs | fr |
dc.type | Article | fr |
dc.contributor.affiliation | Université de Montréal. Faculté de médecine. Département de microbiologie, infectiologie et immunologie | fr |
dc.identifier.doi | 10.1038/s42003-021-02108-y | |
dcterms.abstract | The long-term survival of biomaterial implants is often hampered by surgery-induced inflammation that can lead to graft failure. Considering that most corneas receiving grafts are either pathological or inflamed before implantation, the risk of rejection is heightened. Here, we show that bioengineered, fully synthetic, and robust corneal implants can be manufactured from a collagen analog (collagen-like peptide-polyethylene glycol hybrid, CLP-PEG) and inflammation-suppressing polymeric 2-methacryloyloxyethyl phosphorylcholine (MPC) when stabilized with the triazine-based crosslinker 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride. The resulting CLP-PEG-MPC implants led to reduced corneal swelling, haze, and neovascularization in comparison to CLP-PEG only implants when grafted into a mini-pig cornea alkali burn model of inflammation over 12 months. Implants incorporating MPC allowed for faster nerve regeneration and recovery of corneal sensation. CLP-PEG-MPC implants appear to be at a more advanced stage of regeneration than the CLP-PEG only implants, as evidenced by the presence of higher amounts of cornea-specific type V collagen, and a corresponding decrease in the presence of extracellular vesicles and exosomes in the corneal stroma, in keeping with the amounts present in healthy, unoperated corneas. | fr |
dcterms.isPartOf | urn:ISSN:2399-3642 | fr |
dcterms.language | eng | fr |
UdeM.ReferenceFournieParDeposant | 10.1038/s42003-021-02108-y | fr |
UdeM.VersionRioxx | Version publiée / Version of Record | fr |
oaire.citationTitle | Communications biology | fr |
oaire.citationVolume | 4 | fr |