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Article: A bio-functional polymer that prevents retinal scarring through modulation of NRF2 signalling pathway

TitleA bio-functional polymer that prevents retinal scarring through modulation of NRF2 signalling pathway
Authors
Issue Date2022
Citation
Nature Communications, 2022, v. 13, n. 1, article no. 2796 How to Cite?
AbstractOne common cause of vision loss after retinal detachment surgery is the formation of proliferative and contractile fibrocellular membranes. This aberrant wound healing process is mediated by epithelial-mesenchymal transition (EMT) and hyper-proliferation of retinal pigment epithelial (RPE) cells. Current treatment relies primarily on surgical removal of these membranes. Here, we demonstrate that a bio-functional polymer by itself is able to prevent retinal scarring in an experimental rabbit model of proliferative vitreoretinopathy. This is mediated primarily via clathrin-dependent internalisation of polymeric micelles, downstream suppression of canonical EMT transcription factors, reduction of RPE cell hyper-proliferation and migration. Nuclear factor erythroid 2–related factor 2 signalling pathway was identified in a genome-wide transcriptomic profiling as a key sensor and effector. This study highlights the potential of using synthetic bio-functional polymer to modulate RPE cellular behaviour and offers a potential therapy for retinal scarring prevention.
Persistent Identifierhttp://hdl.handle.net/10722/335883
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorParikh, Bhav Harshad-
dc.contributor.authorLiu, Zengping-
dc.contributor.authorBlakeley, Paul-
dc.contributor.authorLin, Qianyu-
dc.contributor.authorSingh, Malay-
dc.contributor.authorOng, Jun Yi-
dc.contributor.authorHo, Kim Han-
dc.contributor.authorLai, Joel Weijia-
dc.contributor.authorBogireddi, Hanumakumar-
dc.contributor.authorTran, Kim Chi-
dc.contributor.authorLim, Jason Y.C.-
dc.contributor.authorXue, Kun-
dc.contributor.authorAl-Mubaarak, Abdurrahmaan-
dc.contributor.authorYang, Binxia-
dc.contributor.authorSowmiya, R.-
dc.contributor.authorRegha, Kakkad-
dc.contributor.authorWong, Daniel Soo Lin-
dc.contributor.authorTan, Queenie Shu Woon-
dc.contributor.authorZhang, Zhongxing-
dc.contributor.authorJeyasekharan, Anand D.-
dc.contributor.authorBarathi, Veluchamy Amutha-
dc.contributor.authorYu, Weimiao-
dc.contributor.authorCheong, Kang Hao-
dc.contributor.authorBlenkinsop, Timothy A.-
dc.contributor.authorHunziker, Walter-
dc.contributor.authorLingam, Gopal-
dc.contributor.authorLoh, Xian Jun-
dc.contributor.authorSu, Xinyi-
dc.date.accessioned2023-12-28T08:49:27Z-
dc.date.available2023-12-28T08:49:27Z-
dc.date.issued2022-
dc.identifier.citationNature Communications, 2022, v. 13, n. 1, article no. 2796-
dc.identifier.urihttp://hdl.handle.net/10722/335883-
dc.description.abstractOne common cause of vision loss after retinal detachment surgery is the formation of proliferative and contractile fibrocellular membranes. This aberrant wound healing process is mediated by epithelial-mesenchymal transition (EMT) and hyper-proliferation of retinal pigment epithelial (RPE) cells. Current treatment relies primarily on surgical removal of these membranes. Here, we demonstrate that a bio-functional polymer by itself is able to prevent retinal scarring in an experimental rabbit model of proliferative vitreoretinopathy. This is mediated primarily via clathrin-dependent internalisation of polymeric micelles, downstream suppression of canonical EMT transcription factors, reduction of RPE cell hyper-proliferation and migration. Nuclear factor erythroid 2–related factor 2 signalling pathway was identified in a genome-wide transcriptomic profiling as a key sensor and effector. This study highlights the potential of using synthetic bio-functional polymer to modulate RPE cellular behaviour and offers a potential therapy for retinal scarring prevention.-
dc.languageeng-
dc.relation.ispartofNature Communications-
dc.titleA bio-functional polymer that prevents retinal scarring through modulation of NRF2 signalling pathway-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/s41467-022-30474-6-
dc.identifier.pmid35589753-
dc.identifier.scopuseid_2-s2.0-85130317759-
dc.identifier.volume13-
dc.identifier.issue1-
dc.identifier.spagearticle no. 2796-
dc.identifier.epagearticle no. 2796-
dc.identifier.eissn2041-1723-
dc.identifier.isiWOS:000798347800019-

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