A bio-functional polymer that prevents retinal scarring through modulation of NRF2 signalling pathway.
Bhav Harshad ParikhZengping LiuPaul BlakeleyQianyu LinMalay SinghJun Yi OngKim Han HoJoel Weijia LaiHanumakumar BogireddiKim Chi TranChen Chuan LimKun XueAbdurrahmaan Al-MubaarakBinxia YangSowmiya RKakkad ReghaDaniel Soo Lin WongQueenie Shu Woon TanZhongxing ZhangAnand D JeyasekharanVeluchamy Amutha BarathiWeimiao YuKang Hao CheongTimothy A BlenkinsopWalter HunzikerLingam GopalXian Jun LohXinyi SuPublished in: Nature communications (2022)
One 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.
Keyphrases
- epithelial mesenchymal transition
- nuclear factor
- optical coherence tomography
- diabetic retinopathy
- single cell
- genome wide
- signaling pathway
- drug delivery
- induced apoptosis
- transcription factor
- transforming growth factor
- wound healing
- toll like receptor
- optic nerve
- minimally invasive
- dna methylation
- drug release
- cell therapy
- stem cells
- human health
- coronary artery bypass
- dendritic cells
- coronary artery disease
- immune response
- regulatory t cells
- mesenchymal stem cells
- cell death
- cell proliferation
- inflammatory response
- gene expression
- mouse model
- copy number
- smooth muscle
- dna binding
- combination therapy
- bone marrow