idw – Informationsdienst Wissenschaft
Nachrichten, Termine, Experten
Nachrichten, Termine, Experten
idw - Informationsdienst
Wissenschaft
Scientists at the Heart Center of the University Medical Center Göttingen have for the first time found an approach for a personalised therapy option with "gene editing" for the Noonan Syndrome. Publication in the renowned journal "Circulation"
(umg/mbexc) Congenital heart diseases are the most common organ defects. They occur in about one percent of newborns. A large number of genes are involved in a heart dysfunction. For many congenital heart diseases, such as Noonan Syndrome, the link between the genetic changes (mutations) and the heart malformations have not yet been fully understood. The possibilities for treatment are limited. In most cases, they are limited to attenuate the symptoms of the disease.
Scientists at the Heart Center of the University Medical Center Göttingen (UMG) and the Cluster of Excellence “Multiscale Bioimaging” (MBExC) have for the first time been able to identify the link between the underlying gene mutations and the development of heart muscle thickening (heart hypertrophy) for the congenital heart disease Noonan Syndrome. According to their findings, mutations in one gene, the LZTR1 gene, are the cause of the development of symptoms in some previously unexplained clinical cases. The gene regulates essential signaling pathways for cell differentiation and growth. Modified variants of the gene are the starting point for a clinically transferable, personalized therapy option using "gene editing". The results were published in the renowned journal "Circulation".
The interdisciplinary research was carried out under the project lead of Dr. Lukas Cyganek, head of the Stem Cell Unit at the UMG, and Prof. Dr. Bernd Wollnik, director of the Institute for Human Genetics at the UMG. Those involved included the Department of Cardiology and Pneumology (Director: Prof. Dr. Gerd Hasenfuß), the Department of Paediatric and Adolescent Medicine - Paediatric Cardiology, Intensive Care Medicine and Pneumology (Director: Prof. Dr. Thomas Paul) and the Institute of Pharmacology and Toxicology (Director: Prof. Dr. Wolfram-Hubertus Zimmermann) of the UMG. The research was funded by the German Research Foundation (DFG), the Collaborative Research Center 1002, the German Centre for Cardiovascular Research (DZHK), and by the Cluster of Excellence “Multiscale Bioimaging” (MBExC).
Original publication: Ulrich Hanses, Mandy Kleinsorge, Lennart Roos, Gökhan Yigit, Yun Li, Boris Barbarics, Ibrahim El-Battrawy, Huan Lan, Malte Tiburcy, Robin Hindmarsh, Christof Lenz, Gabriela Salinas, Sebastian Diecke, Christian Müller, Ibrahim Adham, Janine Altmüller, Peter Nürnberg, Thomas Paul, Wolfram-Hubertus Zimmermann, Gerd Hasenfuss, Bernd Wollnik, and Lukas Cyganek. Intronic CRISPR Repair in a Preclinical Model of Noonan Syndrome-Associated Cardiomyopathy. Circulation. July 6th, 2020. doi:10.1161/CIRCULATIONAHA.119.044794.
Noonan syndrome is a genetic disease that is associated with developmental disorders. Typical symptoms include growth retardation and dwarfism, facial malfor-mations and serious heart defects. The genetic changes underlying the disease cause an overactivation of the so-called RAS-MAP kinase signaling pathway. This pathway is involved in many biological processes, e.g. cell differentiation and cell growth.
Research findings in Detail
The research group led by Dr. Cyganek and Prof. Dr. Wollnik was able to identify mutations in the LZTR1 gene (leucine zipper like transcription regulator 1) as causative in two affected brothers with severe forms of hypertrophic cardiomyopathy. To this end, skin cells of the brothers were converted into induced pluripotent stem cells (iPS cells) in the cell culture dish and these were then programmed to become heart muscle cells. Using the heart muscle cells obtained in this way, the molecular and functional features of the disease could be investigated in greater detail. The cause of the overactivation of the RAS-MAP kinase signaling pathway, the pathological enlargement of the cells and the changes in the excitation-contraction coupling of the heart could be explained and a molecular signature of the disease could be constructed.
"The deciphering of the causal LZTR1 variants in both patients using state-of-the-art sequencing technologies and variant interpretation by our unique MutationMin-ing(MM) team was the prerequisite to even consider gene correction for scientific analysis," says Prof. Dr. Bernd Wollnik. In addition, the Göttingen researchers found out that the current drug therapy (calcium channel blockers or inhibition of the RAS-MAP kinase signalling pathway) is only partially effective against the symptoms in the heart muscle cells.
The patient-specific iPS cells of both children, which were recreated in the laboratory, responded immediately to a gene correction using CRISPR/Cas9, the so-called "gene scissors": the signaling pathway activity normalized and the thickening of the heart muscles (hypertrophy) decreased. "The use of the iPS cell technology has enabled us to produce artificial heart muscle cells of the patients in the culture dish. They are the key to testing therapy options tailored to the individual patient using CRISPR/Cas9 gene scissors," says Dr. Lukas Cyganek. Further research is now being carried out to determine whether the therapeutic approach using the gene scissors could also be used in the clinic involving patients.
Further Information:
About the heart center at the University Medical Center Göttingen:
https://herzzentrum.umg.eu/
About the MBExC: www.mbexc.de
University Medical Center Göttingen, Georg-August University
Stem Cell Unit
Dr. Lukas Cyganek
phone +49 (0)551 / 39-64280
lukas.cyganek@med.uni-goettingen.de
http://stemcellunit-umg.de/en/about-us/
University Medical Center Göttingen, Georg-August University
Institute for Human Genetics
Prof. Dr. Bernd Wollnik
phone +49 (0)551 /39-67589
bernd.wollnik@med.uni-goettingen.de
https://www.humangenetik-umg.de/en/
University Medical Center Göttingen, Georg-August University
Stem Cell Unit
Dr. Lukas Cyganek
phone +49 (0)551 / 39-64280
lukas.cyganek@med.uni-goettingen.de
http://stemcellunit-umg.de/en/about-us/
University Medical Center Göttingen, Georg-August University
Institute for Human Genetics
Prof. Dr. Bernd Wollnik
phone +49 (0)551 /39-67589
bernd.wollnik@med.uni-goettingen.de
https://www.humangenetik-umg.de/en/
Original publication: Ulrich Hanses, Mandy Kleinsorge, Lennart Roos, Gökhan Yigit, Yun Li, Boris Barbarics, Ibrahim El-Battrawy, Huan Lan, Malte Tiburcy, Robin Hindmarsh, Christof Lenz, Gabriela Salinas, Sebastian Diecke, Christian Müller, Ibrahim Adham, Janine Altmüller, Peter Nürnberg, Thomas Paul, Wolfram-Hubertus Zimmermann, Gerd Hasenfuss, Bernd Wollnik, and Lukas Cyganek. Intronic CRISPR Repair in a Preclinical Model of Noonan Syndrome-Associated Cardiomyopathy. Circulation. July 6th, 2020. doi:10.1161/CIRCULATIONAHA.119.044794.
Dr. Lukas Cyganek, head of the Stem Cell Unit at the University Medical Center Göttingen and last au ...
Photo: hzg/lange
Prof. Dr. Bernd Wollnik, Director of the Institute for Human Genetics at the University Medical Cent ...
Photo: hzg/schmidt
Criteria of this press release:
Journalists
Medicine
transregional, national
Research results, Scientific Publications
English
You can combine search terms with and, or and/or not, e.g. Philo not logy.
You can use brackets to separate combinations from each other, e.g. (Philo not logy) or (Psycho and logy).
Coherent groups of words will be located as complete phrases if you put them into quotation marks, e.g. “Federal Republic of Germany”.
You can also use the advanced search without entering search terms. It will then follow the criteria you have selected (e.g. country or subject area).
If you have not selected any criteria in a given category, the entire category will be searched (e.g. all subject areas or all countries).
