Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/115246
Title: RNA binding protein IGF2BP2 expression is induced by stress in the heart and mediates dilated cardiomyopathy
Author(s): Krumbein, Miriam
Oberman, Froma
Cinnamon, Yuval
Golomb, Mordechai
May, Dalit
Vainer, Gilad
Belzer, Vitali
Meir, Karen
Fridman, Irina
Haybäck, JohannesLook up in the Integrated Authority File of the German National Library
Poelzl, Gerhard
Kehat, Izhak
Beeri, Ronen
Keßler, Sonja M.Look up in the Integrated Authority File of the German National Library
Yisraeli, Joel K.
Issue Date: 2023
Type: Article
Language: English
Abstract: The IGF2BP family of RNA binding proteins consists of three paralogs that regulate intracellular RNA localization, RNA stability, and translational control. Although IGF2BP1 and 3 are oncofetal proteins, IGF2BP2 expression is maintained in many tissues, including the heart, into adulthood. IGF2BP2 is upregulated in cardiomyocytes during cardiac stress and remodeling and returns to normal levels in recovering hearts. We wondered whether IGF2BP2 might play an adaptive role during cardiac stress and recovery. Enhanced expression of an IGF2BP2 transgene in a conditional, inducible mouse line leads to dilated cardiomyopathy (DCM) and death within 3-4 weeks in newborn or adult hearts. Downregulation of the transgene after 2 weeks, however, rescues these mice, with complete recovery by 12 weeks. Hearts overexpressing IGF2BP2 downregulate sarcomeric and mitochondrial proteins and have fragmented mitochondria and elongated, thinner sarcomeres. IGF2BP2 is also upregulated in DCM or myocardial infarction patients. These results suggest that IGF2BP2 may be an attractive target for therapeutic intervention in cardiomyopathies.
URI: https://opendata.uni-halle.de//handle/1981185920/117201
http://dx.doi.org/10.25673/115246
Open Access: Open access publication
License: (CC BY 4.0) Creative Commons Attribution 4.0(CC BY 4.0) Creative Commons Attribution 4.0
Journal Title: Communications biology
Publisher: Springer Nature
Publisher Place: London
Volume: 6
Original Publication: 10.1038/s42003-023-05547-x
Appears in Collections:Open Access Publikationen der MLU

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