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Kuster, G. M.

Publications and source records attributed to Kuster, G. M..

2 recordsLinked to original sources

Screening for pro-adhesive compounds and their relevance as therapeutic approach in Arrhythmogenic Cardiomyopathy

BackgroundArrhythmogenic Cardiomyopathy (ACM) is one of the major causes of sudden cardiac death in young adults. With the underlying patho-mechanisms not well understood, current therapeutic approaches for this genetic disease are solely symptomatic. A recent study demonstrates that loss of cell-cell adhesion is an important initial step leading to ACM. Because loss of cell-cell adhesion is considered a key initial step, we aim to identify new compounds from a drug library, which can restore intercellular adhesion and potentially serve as therapeutics for ACM. MethodsWe established a 2D cell adhesion-based high-throughput platform and screened an FDA-approved drug library. To model loss of intercellular adhesion, human cell lines deficient for the desmosomal adhesion molecule desmoglein-2 (DSG2) were employed and the revealed top candidates were validated in cells expressing different ACM patient mutations. The therapeutic potential of the top hit dexamethasone was evaluated in an inducible ACM disease mouse model using ECG, echocardiography and histology. Phospho-proteomic analysis was applied to investigate protective drug mechanisms. ResultsWe established a set-up to sensitively detect changes in cell-cell adhesion via a high-throughput platform and applied this approach to identify a large pool of adhesion-strengthening compounds in DSG2 deficient cells. The pro-adhesive effect of selected candidates was validated for different ACM patient mutations inducing defective cell cohesion. Importantly, in vivo administration of the selected top pro-adhesive drug dexamethasone rescued impaired right ventricular function in an ACM mouse model. Phospho-proteome analysis suggests modulation of AKT1/AMPK1 signaling and changes in cardiac contractility and junctional components as factors contributing to this protective effect. ConclusionsWe developed an adhesion-based high-throughput screening platform capable of identifying adhesion modulators. We revealed and validated several pro-adhesive compounds and showed a protective effect for the top candidate dexamethasone in an ACM mouse model. This indicates the potential of adhesion-strengthening compounds as therapeutic strategy in ACM and lays the basis for detailed follow-up studies. Moreover, these results and methods can be translated to other diseases with defective desmosomal adhesion. Clinical PerspectiveO_ST_ABSWhat is new?C_ST_ABSO_LIWe developed a novel high-throughput in vitro screening platform to identify compounds that strengthen cell-cell adhesion under conditions of disrupted adhesion, which is a central pathogenetic step in Arrhythmogenic Cardiomyopathy (ACM). C_LIO_LIWith aid of this screen, we identified and validated different compounds from an FDA-approved drug library, which restore disrupted cell-cell adhesion induced by ACM patient mutations including glucocorticoids such as dexamethasone. C_LIO_LIDexamethasone rescued impaired right ventricular function in a novel inducible ACM mouse model and reverted altered AKT1/AMPK1 signaling as well as changes in the phosphorylation state of components of the contractile and junctional apparatus. C_LI What are clinical implications?O_LIWe established a high-throughput cell-cell adhesion screening method as a viable tool for identifying drugs to combat ACM and other diseases featuring impaired desmosomal adhesion. C_LIO_LIWe identified the glucocorticoid dexamethasone as a promising compound to therapeutically approach ACM. C_LIO_LIThis study highlights strengthening of disrupted cell-cell adhesion as a novel therapeutic strategy to treat ACM. C_LI

pathology↗

Defective Desmosomal Adhesion Causes Arrhythmogenic Cardiomyopathy by involving an Integrin-αVβ6/TGF-β Signaling Cascade

BackgroundArrhythmogenic Cardiomyopathy (ACM) is characterized by progressive loss of cardiomyocytes with fibrofatty replacement, systolic dysfunction and life-threatening arrhythmias. A substantial proportion of ACM is caused by mutations in genes of the desmosomal cell-cell adhesion complex, but the underlying mechanisms are not well understood. So far, treatment options are only symptomatic. Here, we investigate the relevance of defective desmosomal adhesion for ACM development and progression. MethodsWe mutated the binding site of desmoglein-2 (DSG2), a crucial desmosomal adhesion molecule in cardiomyocytes. This DSG2-W2A mutation abrogates the tryptophan swap, a central interaction mechanism of DSG2 based on structural data. Impaired adhesive function of DSG2-W2A was confirmed by cell-cell dissociation assays and force spectroscopy measurements by atomic force microscopy. We next generated a DSG2-W2A knock-in mouse model, which was analyzed by echocardiography and histological and bio-molecular techniques including RNA sequencing, transmission electron and super-resolution microscopy. The results were compared to ACM patient samples and their relevance was confirmed in cardiac slice cultures. ResultsThe DSG2-W2A mutation induced impaired binding and desmosomal adhesion dysfunction on cellular and molecular level. Mice bearing this mutation develop a severe cardiac phenotype recalling the characteristics of ACM, including cardiac fibrosis, impaired systolic function and arrhythmia. A comparison of the transcriptome of mutant mice with ACM patient data suggested deregulated integrin-V{beta}6 and subsequent TGF-{beta} signaling as driver of cardiac fibrosis. Accordingly, blocking antibodies targeting integrin-V{beta}6 or inhibition of TGF-{beta} receptor signaling both led to reduced expression of pro-fibrotic markers in cardiac slice cultures. ConclusionsHere, we show that disruption of desmosomal adhesion is sufficient to induce ACM, which confirms the dysfunctional adhesion hypothesis. Mechanistically, deregulation of integrin-V{beta}6 signaling was identified as a central step towards fibrosis. This highlights the value of this model to discern mechanisms of cardiac fibrosis and to identify and test novel treatment options for ACM.

cell biology↗