| http://purl.uniprot.org/citations/34951542 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/34951542 | http://www.w3.org/2000/01/rdf-schema#comment | "Heart failure is often preceded by pathological cardiac hypertrophy, a thickening of the heart musculature driven by complex gene regulatory and signaling processes. The Drosophila heart has great potential as a genetic model for deciphering the underlying mechanisms of cardiac hypertrophy. However, current methods for evaluating hypertrophy of the Drosophila heart are laborious and difficult to carry out reproducibly. Here, we demonstrate that microcomputerized tomography (microCT) is an accessible, highly reproducible method for nondestructive, quantitative analysis of Drosophila heart morphology and size. To validate our microCT approach for analyzing Drosophila cardiac hypertrophy, we show that expression of constitutively active Ras (Ras85DV12), previously shown to cause hypertrophy of the fly heart, results in significant thickening of both adult and larval heart walls when measured from microCT images. We then show using microCT analysis that genetic upregulation of store-operated Ca2+ entry (SOCE) driven by expression of constitutively active Stim (StimCA) or Orai (OraiCA) proteins also results in significant hypertrophy of the Drosophila heart, through a process that specifically depends on Orai Ca2+ influx channels. Intravital imaging of heart contractility revealed significantly reduced end-diastolic and end-systolic dimensions in StimCA- and OraiCA-expressing hearts, consistent with the hypertrophic phenotype. These results demonstrate that increased SOCE activity is an important driver of hypertrophic cardiomyocyte growth, and demonstrate how microCT analysis combined with tractable genetic tools in Drosophila can be used to delineate molecular signaling processes that underlie cardiac hypertrophy and heart failure.NEW & NOTEWORTHY Genetic analysis of Drosophila cardiac hypertrophy holds immense potential for the discovery of new therapeutic targets to prevent and treat heart failure. This potential has been hindered by a lack of rapid and effective methods for analyzing heart size in flies. Here, we demonstrate that analysis of the Drosophila heart with microcomputerized tomography yields accurate and highly reproducible heart size measurements that can be used to analyze heart growth and cardiac hypertrophy in Drosophila."xsd:string |
| http://purl.uniprot.org/citations/34951542 | http://purl.org/dc/terms/identifier | "doi:10.1152/ajpheart.00387.2021"xsd:string |
| http://purl.uniprot.org/citations/34951542 | http://purl.uniprot.org/core/author | "Smyth J.T."xsd:string |
| http://purl.uniprot.org/citations/34951542 | http://purl.uniprot.org/core/author | "Petersen C.E."xsd:string |
| http://purl.uniprot.org/citations/34951542 | http://purl.uniprot.org/core/author | "Tripoli B.A."xsd:string |
| http://purl.uniprot.org/citations/34951542 | http://purl.uniprot.org/core/author | "Schoborg T.A."xsd:string |
| http://purl.uniprot.org/citations/34951542 | http://purl.uniprot.org/core/date | "2022"xsd:gYear |
| http://purl.uniprot.org/citations/34951542 | http://purl.uniprot.org/core/name | "Am J Physiol Heart Circ Physiol"xsd:string |
| http://purl.uniprot.org/citations/34951542 | http://purl.uniprot.org/core/pages | "H296-H309"xsd:string |
| http://purl.uniprot.org/citations/34951542 | http://purl.uniprot.org/core/title | "Analysis of Drosophila cardiac hypertrophy by microcomputerized tomography for genetic dissection of heart growth mechanisms."xsd:string |
| http://purl.uniprot.org/citations/34951542 | http://purl.uniprot.org/core/volume | "322"xsd:string |
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