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High glucose treatment promotes extracellular matrix proteome remodeling in Muller glial cells.

PeerJ 9:e11316 (2021)
Publ. Version/Full Text DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Background. The underlying pathomechanisms in diabetic retinopathy (DR) remain incompletely understood. The aim of this study was to add to the current knowledge about the particular role of retinal Muller glial cells (RMG) in the initial processes of DR.Methods. Applying a quantitative proteomic workflow, we investigated changes of primary porcine RMG under short term high glucose treatment as well as glycolysis inhibition treatment.Results. We revealed significant changes in RMG proteome primarily in proteins building the extracellular matrix (ECM) indicating fundamental remodeling processes of ECM as novel rapid response to high glucose treatment. Among others, Osteopontin (SPP1) as well as its interacting integrins were significantly downregulated and organotypic retinal explant culture confirmed the selective loss of SPP1 in RMG upon treatment. Since SPP1 in the retina has been described neuroprotective for photoreceptors and functions against experimentally induced cell swelling, it's rapid loss under diabetic conditions may point to a direct involvement of RMG to the early neurodegenerative processes driving DR. Data are available via ProteomeXchange with identifier PXDO15879.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Diabetic Retinopathy ; Secreted Phosphoprotein 1 (spp1) ; Osteopontin ; Neurodegeneration ; Organotypic Explant Cultures ; Translational Large Animal Model ; Pig; Data-independent Acquisition; Diabetic-retinopathy; Identification; Proteins; Survival; Cultures; Retina; Edema; Model
Language english
Publication Year 2021
HGF-reported in Year 2021
ISSN (print) / ISBN 2167-8359
e-ISSN 2167-8359
Journal PeerJ
Quellenangaben Volume: 9, Issue: , Pages: , Article Number: e11316 Supplement: ,
Publisher PeerJ
Publishing Place 341-345 Old St, Third Flr, London, Ec1v 9ll, England
Reviewing status Peer reviewed
POF-Topic(s) 30203 - Molecular Targets and Therapies
Research field(s) Enabling and Novel Technologies
PSP Element(s) G-505700-001
A-630700-001
Grants Deutsche Forschungsgemeinschaft
Scopus ID 85106482290
PubMed ID 34046254
Erfassungsdatum 2021-06-23