Morphogenetic control of zebrafish cardiac looping by Bmp signaling
- Autores
- Lombardo, Veronica Andrea; Heise, Melina; Moghtadaei, Motahareh; Bornhorst, Dorothee; Männer, Jörg; Abdelilah Seyfried, Salim
- Año de publicación
- 2019
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Cardiac looping is an essential and highly conserved morphogenetic process that places the different regions of the developing vertebrate heart tube into proximity of their final topographical positions. Highresolution 4D live imaging of mosaically labelled cardiomyocytes reveals distinct cardiomyocyte behaviors that contribute to the deformation of the entire heart tube. Cardiomyocytes acquire a conical cell shape, which is most pronounced at the superior wall of the atrioventricular canal and contributes to S-shaped bending. Torsional deformation close to the outflow tract contributes to a torque-like winding of the entire heart tube between its two poles. Anisotropic growth of cardiomyocytes based on their positions reinforces Sshaping of the heart. During cardiac looping, bone morphogenetic protein pathway signaling is strongest at the future superior wall of the atrioventricular canal. Upon pharmacological or genetic inhibition of bone morphogenetic protein signaling, myocardial cells at the superior wall of the atrioventricular canal maintain cuboidal cell shapes and S-shaped bending is impaired. This description of cellular rearrangements and cardiac looping regulation may also be relevant for understanding the etiology of human congenital heart defects.
Fil: Lombardo, Veronica Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Biología Molecular y Celular de Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Biología Molecular y Celular de Rosario; Argentina. Universidad Nacional de Rosario. Centro de Estudios Interdisciplinarios; Argentina
Fil: Heise, Melina. Institute of Molecular Biology; Alemania
Fil: Moghtadaei, Motahareh. Institute of Molecular Biology; Alemania. Universitat Potsdam; Alemania
Fil: Bornhorst, Dorothee. Institute of Molecular Biology; Alemania. Universitat Potsdam; Alemania
Fil: Männer, Jörg. Göttingen University; Alemania
Fil: Abdelilah Seyfried, Salim. Institute of Molecular Biology; Alemania. Universitat Potsdam; Alemania - Materia
-
BMP
CARDIAC LOOPING
HEMODYNAMICS
WNT
ZEBRAFISH - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/151835
Ver los metadatos del registro completo
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Morphogenetic control of zebrafish cardiac looping by Bmp signalingLombardo, Veronica AndreaHeise, MelinaMoghtadaei, MotaharehBornhorst, DorotheeMänner, JörgAbdelilah Seyfried, SalimBMPCARDIAC LOOPINGHEMODYNAMICSWNTZEBRAFISHhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Cardiac looping is an essential and highly conserved morphogenetic process that places the different regions of the developing vertebrate heart tube into proximity of their final topographical positions. Highresolution 4D live imaging of mosaically labelled cardiomyocytes reveals distinct cardiomyocyte behaviors that contribute to the deformation of the entire heart tube. Cardiomyocytes acquire a conical cell shape, which is most pronounced at the superior wall of the atrioventricular canal and contributes to S-shaped bending. Torsional deformation close to the outflow tract contributes to a torque-like winding of the entire heart tube between its two poles. Anisotropic growth of cardiomyocytes based on their positions reinforces Sshaping of the heart. During cardiac looping, bone morphogenetic protein pathway signaling is strongest at the future superior wall of the atrioventricular canal. Upon pharmacological or genetic inhibition of bone morphogenetic protein signaling, myocardial cells at the superior wall of the atrioventricular canal maintain cuboidal cell shapes and S-shaped bending is impaired. This description of cellular rearrangements and cardiac looping regulation may also be relevant for understanding the etiology of human congenital heart defects.Fil: Lombardo, Veronica Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Biología Molecular y Celular de Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Biología Molecular y Celular de Rosario; Argentina. Universidad Nacional de Rosario. Centro de Estudios Interdisciplinarios; ArgentinaFil: Heise, Melina. Institute of Molecular Biology; AlemaniaFil: Moghtadaei, Motahareh. Institute of Molecular Biology; Alemania. Universitat Potsdam; AlemaniaFil: Bornhorst, Dorothee. Institute of Molecular Biology; Alemania. Universitat Potsdam; AlemaniaFil: Männer, Jörg. Göttingen University; AlemaniaFil: Abdelilah Seyfried, Salim. Institute of Molecular Biology; Alemania. Universitat Potsdam; AlemaniaCompany of Biologists2019-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/151835Lombardo, Veronica Andrea; Heise, Melina; Moghtadaei, Motahareh; Bornhorst, Dorothee; Männer, Jörg; et al.; Morphogenetic control of zebrafish cardiac looping by Bmp signaling; Company of Biologists; Development; 146; 22; 11-2019; 1-130950-1991CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://dev.biologists.org/lookup/doi/10.1242/dev.180091info:eu-repo/semantics/altIdentifier/doi/10.1242/dev.180091info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:53:21Zoai:ri.conicet.gov.ar:11336/151835instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:53:21.972CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Morphogenetic control of zebrafish cardiac looping by Bmp signaling |
title |
Morphogenetic control of zebrafish cardiac looping by Bmp signaling |
spellingShingle |
Morphogenetic control of zebrafish cardiac looping by Bmp signaling Lombardo, Veronica Andrea BMP CARDIAC LOOPING HEMODYNAMICS WNT ZEBRAFISH |
title_short |
Morphogenetic control of zebrafish cardiac looping by Bmp signaling |
title_full |
Morphogenetic control of zebrafish cardiac looping by Bmp signaling |
title_fullStr |
Morphogenetic control of zebrafish cardiac looping by Bmp signaling |
title_full_unstemmed |
Morphogenetic control of zebrafish cardiac looping by Bmp signaling |
title_sort |
Morphogenetic control of zebrafish cardiac looping by Bmp signaling |
dc.creator.none.fl_str_mv |
Lombardo, Veronica Andrea Heise, Melina Moghtadaei, Motahareh Bornhorst, Dorothee Männer, Jörg Abdelilah Seyfried, Salim |
author |
Lombardo, Veronica Andrea |
author_facet |
Lombardo, Veronica Andrea Heise, Melina Moghtadaei, Motahareh Bornhorst, Dorothee Männer, Jörg Abdelilah Seyfried, Salim |
author_role |
author |
author2 |
Heise, Melina Moghtadaei, Motahareh Bornhorst, Dorothee Männer, Jörg Abdelilah Seyfried, Salim |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
BMP CARDIAC LOOPING HEMODYNAMICS WNT ZEBRAFISH |
topic |
BMP CARDIAC LOOPING HEMODYNAMICS WNT ZEBRAFISH |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Cardiac looping is an essential and highly conserved morphogenetic process that places the different regions of the developing vertebrate heart tube into proximity of their final topographical positions. Highresolution 4D live imaging of mosaically labelled cardiomyocytes reveals distinct cardiomyocyte behaviors that contribute to the deformation of the entire heart tube. Cardiomyocytes acquire a conical cell shape, which is most pronounced at the superior wall of the atrioventricular canal and contributes to S-shaped bending. Torsional deformation close to the outflow tract contributes to a torque-like winding of the entire heart tube between its two poles. Anisotropic growth of cardiomyocytes based on their positions reinforces Sshaping of the heart. During cardiac looping, bone morphogenetic protein pathway signaling is strongest at the future superior wall of the atrioventricular canal. Upon pharmacological or genetic inhibition of bone morphogenetic protein signaling, myocardial cells at the superior wall of the atrioventricular canal maintain cuboidal cell shapes and S-shaped bending is impaired. This description of cellular rearrangements and cardiac looping regulation may also be relevant for understanding the etiology of human congenital heart defects. Fil: Lombardo, Veronica Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Biología Molecular y Celular de Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Biología Molecular y Celular de Rosario; Argentina. Universidad Nacional de Rosario. Centro de Estudios Interdisciplinarios; Argentina Fil: Heise, Melina. Institute of Molecular Biology; Alemania Fil: Moghtadaei, Motahareh. Institute of Molecular Biology; Alemania. Universitat Potsdam; Alemania Fil: Bornhorst, Dorothee. Institute of Molecular Biology; Alemania. Universitat Potsdam; Alemania Fil: Männer, Jörg. Göttingen University; Alemania Fil: Abdelilah Seyfried, Salim. Institute of Molecular Biology; Alemania. Universitat Potsdam; Alemania |
description |
Cardiac looping is an essential and highly conserved morphogenetic process that places the different regions of the developing vertebrate heart tube into proximity of their final topographical positions. Highresolution 4D live imaging of mosaically labelled cardiomyocytes reveals distinct cardiomyocyte behaviors that contribute to the deformation of the entire heart tube. Cardiomyocytes acquire a conical cell shape, which is most pronounced at the superior wall of the atrioventricular canal and contributes to S-shaped bending. Torsional deformation close to the outflow tract contributes to a torque-like winding of the entire heart tube between its two poles. Anisotropic growth of cardiomyocytes based on their positions reinforces Sshaping of the heart. During cardiac looping, bone morphogenetic protein pathway signaling is strongest at the future superior wall of the atrioventricular canal. Upon pharmacological or genetic inhibition of bone morphogenetic protein signaling, myocardial cells at the superior wall of the atrioventricular canal maintain cuboidal cell shapes and S-shaped bending is impaired. This description of cellular rearrangements and cardiac looping regulation may also be relevant for understanding the etiology of human congenital heart defects. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-11 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/151835 Lombardo, Veronica Andrea; Heise, Melina; Moghtadaei, Motahareh; Bornhorst, Dorothee; Männer, Jörg; et al.; Morphogenetic control of zebrafish cardiac looping by Bmp signaling; Company of Biologists; Development; 146; 22; 11-2019; 1-13 0950-1991 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/151835 |
identifier_str_mv |
Lombardo, Veronica Andrea; Heise, Melina; Moghtadaei, Motahareh; Bornhorst, Dorothee; Männer, Jörg; et al.; Morphogenetic control of zebrafish cardiac looping by Bmp signaling; Company of Biologists; Development; 146; 22; 11-2019; 1-13 0950-1991 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://dev.biologists.org/lookup/doi/10.1242/dev.180091 info:eu-repo/semantics/altIdentifier/doi/10.1242/dev.180091 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Company of Biologists |
publisher.none.fl_str_mv |
Company of Biologists |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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collection |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842269219067002880 |
score |
13.13397 |