New gene identified in arrhythmogenic cardiomyopathy

New gene identified in arrhythmogenic cardiomyopathy
A section of a normal healthy heart (left) and three locations in a heart from a patient with arrhythmogenic cardiomyopathy. There are a lot more fat cells (large while spheres) in the diseased heart. Cardiomyocytes in the composite region often show signs of degeneration, as well as enhanced ZBTB11 expression. Credit: GPA Lacraz / Hubrecht Institute

Researchers from the group of Eva van Rooij at the Hubrecht Institute have used advanced sequencing technology to better understand the heart disease arrhythmogenic cardiomyopathy, in which heart muscle tissue is replaced by fat cells. Using explanted human hearts, they found regions in which heart muscle was actively degenerated and identified a new gene, ZBTB11, that drives heart muscle cell degradation. The results were published in Cardiovascular Research on 17 May 2022.

Arrhythmogenic cardiomyopathy (ACM) is a familial in which is replaced by fat cells. It can lead to life-threatening, irregular heartbeats. Currently, no therapy exists to cure arrhythmogenic cardiomyopathy and patients may ultimately need a heart transplantation. Therefore, the group of Eva van Rooij at the Hubrecht Institute collaborated with the UMC Utrecht to better understand the process of degeneration in ACM, to ultimately contribute to the identification of new therapeutic targets to treat the disease.

Local differences

Previous studies on ACM used methods that take a snapshot of the gene expression in diseased tissue to aim at understanding what happens in the disease, but lacked the that is required to identify local differences within the heart. Therefore, the Eva van Rooij and her team collaborated with the group of Alexander van Oudenaarden to use a technique called Tomo-Seq, which enabled the researchers to study within different areas of the heart. It turned out that knowing the location of the cells with changed gene activity was key to the discovery of novel areas of heart muscle degeneration.

Human hearts

The researchers used explanted hearts from ACM patients who received a heart transplantation. Heart disease is often studied in cultured cells or animal models, since the use of patient heart tissue is usually not possible. However, due to a collaboration with Aryan Vink from the Pathology Department of UMC Utrecht, the researchers had access to one of the largest and best documented heart tissue biobanks of the world. This gave them the unique opportunity to study the disease process in patient material. The researchers were able to closely look at the patient heart muscle cells that are degenerating, and identified new genes that may play an important role in this process. Among these genes is the transcription factor ZBTB11, a gene that was not previously known to be involved in arrhythmogenic cardiomyopathy.

New gene identified in arrhythmogenic cardiomyopathy
ZBTB11 (red) overexpression in human iPS-derived cardiomyocytes (green: Alpha-actinin), which resulted in degeneration and enhanced cell death. Credit: CJ Boogerd / Hubrecht Institute

Fat cells

The gene ZBTB11 is specifically expressed in the heart muscle cells that are close to the fat cells. The researchers showed that the activity of ZBTB11 induced degeneration of heart muscle cells, a process that is key in arrhythmogenic cardiomyopathy. This indicates that the fatty regions in the heart induce damage to the neighboring heart muscle cells. In the future, the researchers aim to study if heart muscle damage can be slowed down or even reversed in arrhythmogenic cardiomyopathy.

More information: Cornelis J. Boogerd et al, Spatial transcriptomics unveils ZBTB11 as a regulator of cardiomyocyte degeneration in arrhythmogenic cardiomyopathy, Cardiovascular Research (2022). DOI: 10.1093/cvr/cvac072

Journal information: Cardiovascular Research

Provided by Hubrecht Institute
Citation: New gene identified in arrhythmogenic cardiomyopathy (2022, May 24) retrieved 29 November 2023 from
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Explore further

Patient-derived heart cells mimic disease in vitro


Feedback to editors