Physiological homology between Drosophila melanogaster and vertebrate cardiovascular systems

SUMMARY The physiology of the Drosophila melanogaster cardiovascular system remains poorly characterized compared with its vertebrate counterparts. Basic measures of physiological performance remain unknown. It also is unclear whether subtle physiological defects observed in the human cardiovascular...

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Main Authors: Michael A. Choma, Melissa J. Suter, Benjamin J. Vakoc, Brett E. Bouma, Guillermo J. Tearney
Format: Article
Language:English
Published: The Company of Biologists 2011-05-01
Series:Disease Models & Mechanisms
Online Access:http://dmm.biologists.org/content/4/3/411
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spelling doaj-6a21eb73224c45ff832bfc1fc4a687392020-11-24T21:12:24ZengThe Company of BiologistsDisease Models & Mechanisms1754-84031754-84112011-05-014341142010.1242/dmm.005231005231Physiological homology between Drosophila melanogaster and vertebrate cardiovascular systemsMichael A. ChomaMelissa J. SuterBenjamin J. VakocBrett E. BoumaGuillermo J. TearneySUMMARY The physiology of the Drosophila melanogaster cardiovascular system remains poorly characterized compared with its vertebrate counterparts. Basic measures of physiological performance remain unknown. It also is unclear whether subtle physiological defects observed in the human cardiovascular system can be reproduced in D. melanogaster. Here we characterize the cardiovascular physiology of D. melanogaster in its pre-pupal stage by using high-speed dye angiography and optical coherence tomography. The heart has vigorous pulsatile contractions that drive intracardiac, aortic and extracellular-extravascular hemolymph flow. Several physiological measures, including weight-adjusted cardiac output, body-length-adjusted aortic velocities and intracardiac shear forces, are similar to those in the closed vertebrate cardiovascular systems, including that of humans. Extracellular-extravascular flow in the pre-pupal D. melanogaster circulation drives convection-limited fluid transport. To demonstrate homology in heart dysfunction, we showed that, at the pre-pupal stage, a troponin I mutant, held-up2 (hdp2), has impaired systolic and diastolic heart wall velocities. Impaired heart wall velocities occur in the context of a non-dilated phenotype with a mildly depressed fractional shortening. We additionally derive receiver operating characteristic curves showing that heart wall velocity is a potentially powerful discriminator of systolic heart dysfunction. Our results demonstrate physiological homology and support the use of D. melanogaster as an animal model of complex cardiovascular disease.http://dmm.biologists.org/content/4/3/411
collection DOAJ
language English
format Article
sources DOAJ
author Michael A. Choma
Melissa J. Suter
Benjamin J. Vakoc
Brett E. Bouma
Guillermo J. Tearney
spellingShingle Michael A. Choma
Melissa J. Suter
Benjamin J. Vakoc
Brett E. Bouma
Guillermo J. Tearney
Physiological homology between Drosophila melanogaster and vertebrate cardiovascular systems
Disease Models & Mechanisms
author_facet Michael A. Choma
Melissa J. Suter
Benjamin J. Vakoc
Brett E. Bouma
Guillermo J. Tearney
author_sort Michael A. Choma
title Physiological homology between Drosophila melanogaster and vertebrate cardiovascular systems
title_short Physiological homology between Drosophila melanogaster and vertebrate cardiovascular systems
title_full Physiological homology between Drosophila melanogaster and vertebrate cardiovascular systems
title_fullStr Physiological homology between Drosophila melanogaster and vertebrate cardiovascular systems
title_full_unstemmed Physiological homology between Drosophila melanogaster and vertebrate cardiovascular systems
title_sort physiological homology between drosophila melanogaster and vertebrate cardiovascular systems
publisher The Company of Biologists
series Disease Models & Mechanisms
issn 1754-8403
1754-8411
publishDate 2011-05-01
description SUMMARY The physiology of the Drosophila melanogaster cardiovascular system remains poorly characterized compared with its vertebrate counterparts. Basic measures of physiological performance remain unknown. It also is unclear whether subtle physiological defects observed in the human cardiovascular system can be reproduced in D. melanogaster. Here we characterize the cardiovascular physiology of D. melanogaster in its pre-pupal stage by using high-speed dye angiography and optical coherence tomography. The heart has vigorous pulsatile contractions that drive intracardiac, aortic and extracellular-extravascular hemolymph flow. Several physiological measures, including weight-adjusted cardiac output, body-length-adjusted aortic velocities and intracardiac shear forces, are similar to those in the closed vertebrate cardiovascular systems, including that of humans. Extracellular-extravascular flow in the pre-pupal D. melanogaster circulation drives convection-limited fluid transport. To demonstrate homology in heart dysfunction, we showed that, at the pre-pupal stage, a troponin I mutant, held-up2 (hdp2), has impaired systolic and diastolic heart wall velocities. Impaired heart wall velocities occur in the context of a non-dilated phenotype with a mildly depressed fractional shortening. We additionally derive receiver operating characteristic curves showing that heart wall velocity is a potentially powerful discriminator of systolic heart dysfunction. Our results demonstrate physiological homology and support the use of D. melanogaster as an animal model of complex cardiovascular disease.
url http://dmm.biologists.org/content/4/3/411
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