-
Je něco špatně v tomto záznamu ?
Morphological, electrophysiological, and molecular alterations in foetal noncompacted cardiomyopathy induced by disruption of ROCK signalling
D. Sedmera, V. Olejnickova, B. Sankova, H. Kolesova, M. Bartos, A. Kvasilova, LC. Phillips, SD. Bamforth, HM. Phillips
Status neindexováno Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2013
Free Medical Journals
od 2013
PubMed Central
od 2013
Europe PubMed Central
od 2013
Open Access Digital Library
od 2013-01-01
Open Access Digital Library
od 2013-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2013
- Publikační typ
- časopisecké články MeSH
Left ventricular noncompaction cardiomyopathy is associated with heart failure, arrhythmia, and sudden cardiac death. The developmental mechanism underpinning noncompaction in the adult heart is still not fully understood, with lack of trabeculae compaction, hypertrabeculation, and loss of proliferation cited as possible causes. To study this, we utilised a mouse model of aberrant Rho kinase (ROCK) signalling in cardiomyocytes, which led to a noncompaction phenotype during embryogenesis, and monitored how this progressed after birth and into adulthood. The cause of the early noncompaction at E15.5 was attributed to a decrease in proliferation in the developing ventricular wall. By E18.5, the phenotype became patchy, with regions of noncompaction interspersed with thick compacted areas of ventricular wall. To study how this altered myoarchitecture of the heart influenced impulse propagation in the developing and adult heart, we used histology with immunohistochemistry for gap junction protein expression, optical mapping, and electrocardiography. At the prenatal stages, a clear reduction in left ventricular wall thickness, accompanied by abnormal conduction of the ectopically paced beat in that area, was observed in mutant hearts. This correlated with increased expression of connexin-40 and connexin-43 in noncompacted trabeculae. In postnatal stages, left ventricular noncompaction was resolved, but the right ventricular wall remained structurally abnormal through to adulthood with cardiomyocyte hypertrophy and retention of myocardial crypts. Thus, this is a novel model of self-correcting embryonic hypertrabeculation cardiomyopathy, but it highlights that remodelling potential differs between the left and right ventricles. We conclude that disruption of ROCK signalling induces both morphological and electrophysiological changes that evolve over time, highlighting the link between myocyte proliferation and noncompaction phenotypes and electrophysiological differentiation.
Biosciences Institute Newcastle University Newcastle upon Tyne United Kingdom
Institute of Anatomy 1st Faculty of Medicine Charles University Prague Czechia
Institute of Dental Medicine 1st Faculty of Medicine Charles University Prague Czechia
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25002410
- 003
- CZ-PrNML
- 005
- 20250123101925.0
- 007
- ta
- 008
- 250117e20241007sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3389/fcell.2024.1471751 $2 doi
- 035 __
- $a (PubMed)39435333
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Sedmera, David $u Institute of Anatomy, First Faculty of Medicine, Charles University, Prague, Czechia $u Laboratory of Developmental Cardiology, Institute of Physiology, Czech Academy of Sciences, Prague, Czechia
- 245 10
- $a Morphological, electrophysiological, and molecular alterations in foetal noncompacted cardiomyopathy induced by disruption of ROCK signalling / $c D. Sedmera, V. Olejnickova, B. Sankova, H. Kolesova, M. Bartos, A. Kvasilova, LC. Phillips, SD. Bamforth, HM. Phillips
- 520 9_
- $a Left ventricular noncompaction cardiomyopathy is associated with heart failure, arrhythmia, and sudden cardiac death. The developmental mechanism underpinning noncompaction in the adult heart is still not fully understood, with lack of trabeculae compaction, hypertrabeculation, and loss of proliferation cited as possible causes. To study this, we utilised a mouse model of aberrant Rho kinase (ROCK) signalling in cardiomyocytes, which led to a noncompaction phenotype during embryogenesis, and monitored how this progressed after birth and into adulthood. The cause of the early noncompaction at E15.5 was attributed to a decrease in proliferation in the developing ventricular wall. By E18.5, the phenotype became patchy, with regions of noncompaction interspersed with thick compacted areas of ventricular wall. To study how this altered myoarchitecture of the heart influenced impulse propagation in the developing and adult heart, we used histology with immunohistochemistry for gap junction protein expression, optical mapping, and electrocardiography. At the prenatal stages, a clear reduction in left ventricular wall thickness, accompanied by abnormal conduction of the ectopically paced beat in that area, was observed in mutant hearts. This correlated with increased expression of connexin-40 and connexin-43 in noncompacted trabeculae. In postnatal stages, left ventricular noncompaction was resolved, but the right ventricular wall remained structurally abnormal through to adulthood with cardiomyocyte hypertrophy and retention of myocardial crypts. Thus, this is a novel model of self-correcting embryonic hypertrabeculation cardiomyopathy, but it highlights that remodelling potential differs between the left and right ventricles. We conclude that disruption of ROCK signalling induces both morphological and electrophysiological changes that evolve over time, highlighting the link between myocyte proliferation and noncompaction phenotypes and electrophysiological differentiation.
- 590 __
- $a NEINDEXOVÁNO
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Olejnickova, Veronika $u Institute of Anatomy, First Faculty of Medicine, Charles University, Prague, Czechia
- 700 1_
- $a Sankova, Barbora $u Institute of Anatomy, First Faculty of Medicine, Charles University, Prague, Czechia
- 700 1_
- $a Kolesova, Hana $u Institute of Anatomy, First Faculty of Medicine, Charles University, Prague, Czechia
- 700 1_
- $a Bartos, Martin $u Institute of Anatomy, First Faculty of Medicine, Charles University, Prague, Czechia $u Institute of Dental Medicine, First Faculty of Medicine, Charles University, Prague, Czechia
- 700 1_
- $a Kvasilova, Alena $u Institute of Anatomy, First Faculty of Medicine, Charles University, Prague, Czechia
- 700 1_
- $a Phillips, Lauren C $u Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom
- 700 1_
- $a Bamforth, Simon D $u Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom
- 700 1_
- $a Phillips, Helen M $u Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom
- 773 0_
- $w MED00186212 $t Frontiers in cell and developmental biology. $x 2296-634X $g Roč. 12 (20241007), s. 1471751
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/39435333 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250117 $b ABA008
- 991 __
- $a 20250123101919 $b ABA008
- 999 __
- $a ok $b bmc $g 2254565 $s 1238413
- BAS __
- $a 3
- BAS __
- $a PreBMC-PubMed-not-MEDLINE
- BMC __
- $a 2024 $b 12 $c - $d 1471751 $e 20241007 $i 2296-634X $m Frontiers in cell and developmental biology. $n Front Cell Dev Biol $x MED00186212
- LZP __
- $a Pubmed-20250117