Identifying the evolutionary building blocks of the cardiac conduction system.

The endothermic state of mammals and birds requires high heart rates to accommodate the high rates of oxygen consumption. These high heart rates are driven by very similar conduction systems consisting of an atrioventricular node that slows the electrical impulse and a His-Purkinje system that effic...

Full description

Saved in:
Bibliographic Details
Main Authors: Bjarke Jensen, Bastiaan J D Boukens, Alex V Postma, Quinn D Gunst, Maurice J B van den Hoff, Antoon F M Moorman, Tobias Wang, Vincent M Christoffels
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0044231&type=printable
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850025476361289728
author Bjarke Jensen
Bastiaan J D Boukens
Alex V Postma
Quinn D Gunst
Maurice J B van den Hoff
Antoon F M Moorman
Tobias Wang
Vincent M Christoffels
author_facet Bjarke Jensen
Bastiaan J D Boukens
Alex V Postma
Quinn D Gunst
Maurice J B van den Hoff
Antoon F M Moorman
Tobias Wang
Vincent M Christoffels
author_sort Bjarke Jensen
collection DOAJ
description The endothermic state of mammals and birds requires high heart rates to accommodate the high rates of oxygen consumption. These high heart rates are driven by very similar conduction systems consisting of an atrioventricular node that slows the electrical impulse and a His-Purkinje system that efficiently activates the ventricular chambers. While ectothermic vertebrates have similar contraction patterns, they do not possess anatomical evidence for a conduction system. This lack amongst extant ectotherms is surprising because mammals and birds evolved independently from reptile-like ancestors. Using conserved genetic markers, we found that the conduction system design of lizard (Anolis carolinensis and A. sagrei), frog (Xenopus laevis) and zebrafish (Danio rerio) adults is strikingly similar to that of embryos of mammals (mouse Mus musculus, and man) and chicken (Gallus gallus). Thus, in ectothermic adults, the slow conducting atrioventricular canal muscle is present, no fibrous insulating plane is formed, and the spongy ventricle serves the dual purpose of conduction and contraction. Optical mapping showed base-to-apex activation of the ventricles of the ectothermic animals, similar to the activation pattern of mammalian and avian embryonic ventricles and to the His-Purkinje systems of the formed hearts. Mammalian and avian ventricles uniquely develop thick compact walls and septum and, hence, form a discrete ventricular conduction system from the embryonic spongy ventricle. Our study uncovers the evolutionary building plan of heart and indicates that the building blocks of the conduction system of adult ectothermic vertebrates and embryos of endotherms are similar.
format Article
id doaj-art-ecdb97e5aae04551b378dd3edab57a63
institution DOAJ
issn 1932-6203
language English
publishDate 2012-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj-art-ecdb97e5aae04551b378dd3edab57a632025-08-20T03:00:50ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0179e4423110.1371/journal.pone.0044231Identifying the evolutionary building blocks of the cardiac conduction system.Bjarke JensenBastiaan J D BoukensAlex V PostmaQuinn D GunstMaurice J B van den HoffAntoon F M MoormanTobias WangVincent M ChristoffelsThe endothermic state of mammals and birds requires high heart rates to accommodate the high rates of oxygen consumption. These high heart rates are driven by very similar conduction systems consisting of an atrioventricular node that slows the electrical impulse and a His-Purkinje system that efficiently activates the ventricular chambers. While ectothermic vertebrates have similar contraction patterns, they do not possess anatomical evidence for a conduction system. This lack amongst extant ectotherms is surprising because mammals and birds evolved independently from reptile-like ancestors. Using conserved genetic markers, we found that the conduction system design of lizard (Anolis carolinensis and A. sagrei), frog (Xenopus laevis) and zebrafish (Danio rerio) adults is strikingly similar to that of embryos of mammals (mouse Mus musculus, and man) and chicken (Gallus gallus). Thus, in ectothermic adults, the slow conducting atrioventricular canal muscle is present, no fibrous insulating plane is formed, and the spongy ventricle serves the dual purpose of conduction and contraction. Optical mapping showed base-to-apex activation of the ventricles of the ectothermic animals, similar to the activation pattern of mammalian and avian embryonic ventricles and to the His-Purkinje systems of the formed hearts. Mammalian and avian ventricles uniquely develop thick compact walls and septum and, hence, form a discrete ventricular conduction system from the embryonic spongy ventricle. Our study uncovers the evolutionary building plan of heart and indicates that the building blocks of the conduction system of adult ectothermic vertebrates and embryos of endotherms are similar.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0044231&type=printable
spellingShingle Bjarke Jensen
Bastiaan J D Boukens
Alex V Postma
Quinn D Gunst
Maurice J B van den Hoff
Antoon F M Moorman
Tobias Wang
Vincent M Christoffels
Identifying the evolutionary building blocks of the cardiac conduction system.
PLoS ONE
title Identifying the evolutionary building blocks of the cardiac conduction system.
title_full Identifying the evolutionary building blocks of the cardiac conduction system.
title_fullStr Identifying the evolutionary building blocks of the cardiac conduction system.
title_full_unstemmed Identifying the evolutionary building blocks of the cardiac conduction system.
title_short Identifying the evolutionary building blocks of the cardiac conduction system.
title_sort identifying the evolutionary building blocks of the cardiac conduction system
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0044231&type=printable
work_keys_str_mv AT bjarkejensen identifyingtheevolutionarybuildingblocksofthecardiacconductionsystem
AT bastiaanjdboukens identifyingtheevolutionarybuildingblocksofthecardiacconductionsystem
AT alexvpostma identifyingtheevolutionarybuildingblocksofthecardiacconductionsystem
AT quinndgunst identifyingtheevolutionarybuildingblocksofthecardiacconductionsystem
AT mauricejbvandenhoff identifyingtheevolutionarybuildingblocksofthecardiacconductionsystem
AT antoonfmmoorman identifyingtheevolutionarybuildingblocksofthecardiacconductionsystem
AT tobiaswang identifyingtheevolutionarybuildingblocksofthecardiacconductionsystem
AT vincentmchristoffels identifyingtheevolutionarybuildingblocksofthecardiacconductionsystem