Jacob, Fabian, Yonis, Amina Y., Cuello, Friederike, Luther, Pradeep ORCID: 0000-0002-8841-4368, Schulze, Thomas, Eder, Alexandra, Streichert, Thomas, Mannhardt, Ingra, Hirt, Marc N., Schaaf, Sebastian, Stenzig, Justus, Force, Thomas ORCID: 0000-0002-0450-8659, Eschenhagen, Thomas and Hansen, Arne (2016). Analysis of Tyrosine Kinase Inhibitor-Mediated Decline in Contractile Force in Rat Engineered Heart Tissue. PLoS One, 11 (2). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203

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Abstract

Introduction Left ventricular dysfunction is a frequent and potentially severe side effect of many tyrosine kinase inhibitors (TKI). The mode of toxicity is not identified, but may include impairment of mitochondrial or sarcomeric function, autophagy or angiogenesis, either as an on-target or off-target mechanism. Methods and Results We studied concentration-response curves and time courses for nine TKIs in three-dimensional, force generating engineered heart tissue (EHT) from neonatal rat heart cells. We detected a concentration-and time-dependent decline in contractile force for gefitinib, lapatinib, sunitinib, imatinib, sorafenib, vandetanib and lestaurtinib and no decline in contractile force for erlotinib and dasatinib after 96 hours of incubation. The decline in contractile force was associated with an impairment of autophagy (LC3 Western blot) and appearance of autophagolysosomes (transmission electron microscopy). Conclusion This study demonstrates the feasibility to study TKI-mediated force effects in EHTs and identifies an association between a decline in contractility and inhibition of autophagic flux.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Jacob, FabianUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Yonis, Amina Y.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Cuello, FriederikeUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Luther, PradeepUNSPECIFIEDorcid.org/0000-0002-8841-4368UNSPECIFIED
Schulze, ThomasUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Eder, AlexandraUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Streichert, ThomasUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Mannhardt, IngraUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hirt, Marc N.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Schaaf, SebastianUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Stenzig, JustusUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Force, ThomasUNSPECIFIEDorcid.org/0000-0002-0450-8659UNSPECIFIED
Eschenhagen, ThomasUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hansen, ArneUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-284788
DOI: 10.1371/journal.pone.0145937
Journal or Publication Title: PLoS One
Volume: 11
Number: 2
Date: 2016
Publisher: PUBLIC LIBRARY SCIENCE
Place of Publication: SAN FRANCISCO
ISSN: 1932-6203
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
INDUCED CARDIOTOXICITY; CELL-DEATH; IN-VITRO; IMATINIB; MITOCHONDRIA; MECHANISMS; SUNITINIB; AUTOPHAGY; CARDIOMYOCYTES; SORAFENIBMultiple languages
Multidisciplinary SciencesMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/28478

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