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Biomechanical signaling within the developing zebrafish heart attunes endocardial growth to myocardial chamber dimensions

  • Intra-organ communication guides morphogenetic processes that are essential for an organ to carry out complex physiological functions. In the heart, the growth of the myocardium is tightly coupled to that of the endocardium, a specialized endothelial tissue that lines its interior. Several molecular pathways have been implicated in the communication between these tissues including secreted factors, components of the extracellular matrix, or proteins involved in cell-cell communication. Yet, it is unknown how the growth of the endocardium is coordinated with that of the myocardium. Here, we show that an increased expansion of the myocardial atrial chamber volume generates higher junctional forces within endocardial cells. This leads to biomechanical signaling involving VE-cadherin, triggering nuclear localization of the Hippo pathway transcriptional regulator Yap1 and endocardial proliferation. Our work suggests that the growth of the endocardium results from myocardial chamber volume expansion and ends when the tension on the tissueIntra-organ communication guides morphogenetic processes that are essential for an organ to carry out complex physiological functions. In the heart, the growth of the myocardium is tightly coupled to that of the endocardium, a specialized endothelial tissue that lines its interior. Several molecular pathways have been implicated in the communication between these tissues including secreted factors, components of the extracellular matrix, or proteins involved in cell-cell communication. Yet, it is unknown how the growth of the endocardium is coordinated with that of the myocardium. Here, we show that an increased expansion of the myocardial atrial chamber volume generates higher junctional forces within endocardial cells. This leads to biomechanical signaling involving VE-cadherin, triggering nuclear localization of the Hippo pathway transcriptional regulator Yap1 and endocardial proliferation. Our work suggests that the growth of the endocardium results from myocardial chamber volume expansion and ends when the tension on the tissue is relaxed.zeige mehrzeige weniger

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Metadaten
Verfasserangaben:Dorothee BornhorstORCiDGND, Peng XiaORCiDGND, Hiroyuki NakajimaORCiD, Chaitanya DingareORCiD, Wiebke HerzogORCiD, Virginie LecaudeyORCiDGND, Naoki MochizukiORCiD, Carl-Philipp HeisenbergORCiDGND, Deborah YelonORCiD, Salim Abdelilah-SeyfriedORCiDGND
DOI:https://doi.org/10.1038/s41467-019-12068-x
ISSN:2041-1723
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/31511517
Titel des übergeordneten Werks (Englisch):Nature Communications
Verlag:Nature Publ. Group
Verlagsort:London
Publikationstyp:Wissenschaftlicher Artikel
Sprache:Englisch
Datum der Erstveröffentlichung:11.09.2019
Erscheinungsjahr:2019
Datum der Freischaltung:24.11.2020
Band:10
Seitenanzahl:10
Fördernde Institution:Excellence cluster REBIRTH; Deutsche Forschungsgemeinschaft (DFG)German Research Foundation (DFG) [SE2016/7-2, SE2016/10-1]; DZHK; NIHUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USA [R01 HL069594, R01 HL108599]; Excellence cluster REBIRTH [SFB958]
Organisationseinheiten:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
DDC-Klassifikation:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Peer Review:Referiert
Publikationsweg:Open Access
Open Access / Gold Open-Access
DOAJ gelistet
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