Literature DB >> 27639425

Sarcomeric lesions and remodeling proximal to intercalated disks in overload-induced cardiac hypertrophy.

Sied Kebir1, Zacharias Orfanos2, Julia Schuld3, Markus Linhart4, Christian Lamberz5, Peter F M van der Ven6, Jan Schrickel7, Gregor Kirfel8, Dieter O Fürst9, Rainer Meyer10.   

Abstract

Pressure overload induces cardiac remodeling involving both the contractile machinery and intercalated disks (IDs). Filamin C (FlnC) and Xin actin-binding repeat-containing proteins (XIRPs) are multi-adapters localizing in IDs of higher vertebrates. Knockout of the gene encoding Xin (Xirp1) in mice leads to a mild cardiac phenotype with ID mislocalization. In order to amplify this phenotype, we performed transverse aortic constriction (TAC) on control and Xirp1-deficient mice. TAC induced similar left ventricular hypertrophy in both genotypes, suggesting that the lack of Xin does not lead to higher susceptibility to cardiac overload. However, in both genotypes, FlnC appeared in "streaming" localizations across multiple sarcomeres proximal to the IDs, suggesting a remodeling response. Furthermore, FlnC-positive areas of remodeling, reminiscent of sarcomeric lesions previously described for skeletal muscles (but so far unreported in the heart), were also observed. These adaptations reflect a similarly strong effect of the pressure induced by TAC in both genotypes. However, 2 weeks post-operation TAC-treated knockout hearts had reduced levels of connexin43 and slightly increased incidents of ventricular tachycardia compared to their wild-type (WT) counterparts. Our findings highlight the FlnC-positive sarcomeric lesions and ID-proximal streaming as general remodeling responses in cardiac overload-induced hypertrophy.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Connexin43; Cross-striated muscle cells; Filamin C; XIRP2; Xin actin-binding repeat-containing proteins; Xirp1

Mesh:

Substances:

Year:  2016        PMID: 27639425     DOI: 10.1016/j.yexcr.2016.09.008

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  4 in total

1.  The p.Ala2430Val mutation in filamin C causes a "hypertrophic myofibrillar cardiomyopathy".

Authors:  Julia Schuld; Peter F M van der Ven; Anne Schänzer; Elisabeth Schumann; Diana Zengeler; Lisann Gulatz; Giovanni Maroli; Uwe Ahting; Anke Sprengel; Sabine Gräf; Andreas Hahn; Christian Jux; Till Acker; Dieter O Fürst; Stefan Rupp
Journal:  J Muscle Res Cell Motil       Date:  2021-03-12       Impact factor: 2.698

2.  Transcriptome Analysis of Cardiac Hypertrophic Growth in MYBPC3-Null Mice Suggests Early Responders in Hypertrophic Remodeling.

Authors:  Emily Farrell; Annie E Armstrong; Adrian C Grimes; Francisco J Naya; Willem J de Lange; J Carter Ralphe
Journal:  Front Physiol       Date:  2018-10-25       Impact factor: 4.566

3.  Homozygous expression of the myofibrillar myopathy-associated p.W2710X filamin C variant reveals major pathomechanisms of sarcomeric lesion formation.

Authors:  Julia Schuld; Zacharias Orfanos; Frédéric Chevessier; Britta Eggers; Lorena Heil; Julian Uszkoreit; Andreas Unger; Gregor Kirfel; Peter F M van der Ven; Katrin Marcus; Wolfgang A Linke; Christoph S Clemen; Rolf Schröder; Dieter O Fürst
Journal:  Acta Neuropathol Commun       Date:  2020-09-04       Impact factor: 7.801

4.  miR-125 family regulates XIRP1 and FIH in response to myocardial infarction.

Authors:  Allison Lesher Williams; Vedbar S Khadka; Ma C T Anagaran; Katie Lee; Abigail Avelar; Youping Deng; Ralph V Shohet
Journal:  Physiol Genomics       Date:  2020-07-27       Impact factor: 3.107

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.