细胞外基质
路径(计算)
医学
计算机科学
计算生物学
生物
细胞生物学
程序设计语言
作者
Laura Bianchi,Annalisa Altera,Virginia Barone,Denise Bonente,Tommaso Bacci,Elena De Benedetto,Luca Bini,Gian Marco Tosi,Federico Galvagni,Eugenio Bertelli
出处
期刊:Cells
[MDPI AG]
日期:2022-08-15
卷期号:11 (16): 2531-2531
被引量:13
标识
DOI:10.3390/cells11162531
摘要
Idiopathic epiretinal membranes (iERMs) are fibrocellular sheets of tissue that develop at the vitreoretinal interface. The iERMs consist of cells and an extracellular matrix (ECM) formed by a complex array of structural proteins and a large number of proteins that regulate cell-matrix interaction, matrix deposition and remodelling. Many components of the ECM tend to produce a layered pattern that can influence the tractional properties of the membranes. We applied a bioinformatics approach on a list of proteins previously identified with an MS-based proteomic analysis on samples of iERM to report the interactome of some key proteins. The performed pathway analysis highlights interactions occurring among ECM molecules, their cell receptors and intra- or extracellular proteins that may play a role in matrix biology in this special context. In particular, integrin β1, cathepsin B, epidermal growth factor receptor, protein-glutamine gamma-glutamyltransferase 2 and prolow-density lipoprotein receptor-related protein 1 are key hubs in the outlined protein-protein cross-talks. A section on the biomarkers that can be found in the vitreous humor of patients affected by iERM and that can modulate matrix deposition is also presented. Finally, translational medicine in iERM treatment has been summed up taking stock of the techniques that have been proposed for pharmacologic vitreolysis.
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