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Therapeutic Validation of GEF-H1 Using a De Novo Designed Inhibitor in Models of Retinal Disease

Title: Therapeutic Validation of GEF-H1 Using a De Novo Designed Inhibitor in Models of Retinal Disease
Authors: Mills, Clare; Hemkemeyer, Sandra A; Alimajstorovic, Zerin; Bowers, Chantelle; Eskandarpour, Malihe; Greenwood, John; Calder, Virginia; Chan, AW Edith; Gane, Paul J; Selwood, David L; Matter, Karl; Balda, Maria S
Source: Cells , 11 (11) , Article 1733. (2022)
Publisher Information: MDPI AG
Publication Year: 2022
Collection: University College London: UCL Discovery
Subject Terms: RhoA; tight junctions; inflammation; retinal pigment epithelium; endothelium
Description: Inflammation and fibrosis are important components of diseases that contribute to the malfunction of epithelia and endothelia. The Rho guanine nucleotide exchange factor (GEF) GEF-H1/ARHGEF-2 is induced in disease and stimulates inflammatory and fibrotic processes, cell migration, and metastasis. Here, we have generated peptide inhibitors to block the function of GEF-H1. Inhibitors were designed using a structural in silico approach or by isolating an inhibitory sequence from the autoregulatory C-terminal domain. Candidate inhibitors were tested for their ability to block RhoA/GEF-H1 binding in vitro, and their potency and specificity in cell-based assays. Successful inhibitors were then evaluated in models of TGFβ-induced fibrosis, LPS-stimulated endothelial cell-cell junction disruption, and cell migration. Finally, the most potent inhibitor was successfully tested in an experimental retinal disease mouse model, in which it inhibited blood vessel leakage and ameliorated retinal inflammation when treatment was initiated after disease diagnosis. Thus, an antagonist that blocks GEF-H1 signaling effectively inhibits disease features in in vitro and in vivo disease models, demonstrating that GEF-H1 is an effective therapeutic target and establishing a new therapeutic approach.
Document Type: article in journal/newspaper
File Description: text
Language: English
Relation: https://discovery.ucl.ac.uk/id/eprint/10149818/
Availability: https://discovery.ucl.ac.uk/id/eprint/10149818/1/Greenwood_Therapeutic%20Validation%20of%20GEF-H1%20Using%20a%20De%20Novo%20Designed%20Inhibitor%20in%20Models%20of%20Retinal%20Disease_VoR.pdf; https://discovery.ucl.ac.uk/id/eprint/10149818/
Rights: open
Accession Number: edsbas.4DA658F
Database: BASE