Literature DB >> 34696883

Endothelial mechanotransduction in cardiovascular development and regeneration: emerging approaches and animal models.

Susana Cavallero1, Ana M Blázquez-Medela1, Sandro Satta1, Tzung K Hsiai2.   

Abstract

Living cells are exposed to multiple mechanical stimuli from the extracellular matrix or from surrounding cells. Mechanoreceptors are molecules that display status changes in response to mechanical stimulation, transforming physical cues into biological responses to help the cells adapt to dynamic changes of the microenvironment. Mechanical stimuli are responsible for shaping the tridimensional development and patterning of the organs in early embryonic stages. The development of the heart is one of the first morphogenetic events that occur in embryos. As the circulation is established, the vascular system is exposed to constant shear stress, which is the force created by the movement of blood. Both spatial and temporal variations in shear stress differentially modulate critical steps in heart development, such as trabeculation and compaction of the ventricular wall and the formation of the heart valves. Zebrafish embryos are small, transparent, have a short developmental period and allow for real-time visualization of a variety of fluorescently labeled proteins to recapitulate developmental dynamics. In this review, we will highlight the application of zebrafish models as a genetically tractable model for investigating cardiovascular development and regeneration. We will introduce our approaches to manipulate mechanical forces during critical stages of zebrafish heart development and in a model of vascular regeneration, as well as advances in imaging technologies to capture these processes at high resolution. Finally, we will discuss the role of molecules of the Plexin family and Piezo cation channels as major mechanosensors recently implicated in cardiac morphogenesis.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Light sheet microscopy; Mechanotransduction; Notch; Shear stress; Trabeculation; Zebrafish

Mesh:

Year:  2021        PMID: 34696883      PMCID: PMC9113082          DOI: 10.1016/bs.ctm.2021.07.002

Source DB:  PubMed          Journal:  Curr Top Membr        ISSN: 1063-5823            Impact factor:   2.025


  90 in total

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Journal:  Cell       Date:  2013-08-01       Impact factor: 41.582

2.  Contractile and hemodynamic forces coordinate Notch1b-mediated outflow tract valve formation.

Authors:  Jeffrey J Hsu; Vijay Vedula; Kyung In Baek; Cynthia Chen; Junjie Chen; Man In Chou; Jeffrey Lam; Shivani Subhedar; Jennifer Wang; Yichen Ding; Chih-Chiang Chang; Juhyun Lee; Linda L Demer; Yin Tintut; Alison L Marsden; Tzung K Hsiai
Journal:  JCI Insight       Date:  2019-04-11

3.  Piezo1 is required for outflow tract and aortic valve development.

Authors:  Adèle Faucherre; Hamid Moha Ou Maati; Nathalie Nasr; Amélie Pinard; Alexis Theron; Gaëlle Odelin; Jean-Pierre Desvignes; David Salgado; Gwenaëlle Collod-Béroud; Jean-François Avierinos; Guillaume Lebon; Stéphane Zaffran; Chris Jopling
Journal:  J Mol Cell Cardiol       Date:  2020-04-03       Impact factor: 5.000

4.  A comparative map of the zebrafish genome.

Authors:  I G Woods; P D Kelly; F Chu; P Ngo-Hazelett; Y L Yan; H Huang; J H Postlethwait; W S Talbot
Journal:  Genome Res       Date:  2000-12       Impact factor: 9.043

5.  Shear stress-induced changes in atherosclerotic plaque composition are modulated by chemokines.

Authors:  Caroline Cheng; Dennie Tempel; Rien van Haperen; Hetty C de Boer; Dolf Segers; Martin Huisman; Anton Jan van Zonneveld; Pieter J M Leenen; Anton van der Steen; Patrick W Serruys; Rini de Crom; Rob Krams
Journal:  J Clin Invest       Date:  2007-02-15       Impact factor: 14.808

Review 6.  Heart valve development: regulatory networks in development and disease.

Authors:  Michelle D Combs; Katherine E Yutzey
Journal:  Circ Res       Date:  2009-08-28       Impact factor: 17.367

7.  Repulsive and attractive semaphorins cooperate to direct the navigation of cardiac neural crest cells.

Authors:  Toshihiko Toyofuku; Junko Yoshida; Tamiko Sugimoto; Midori Yamamoto; Nobuhiko Makino; Hyota Takamatsu; Noriko Takegahara; Fumikazu Suto; Masatsugu Hori; Hajime Fujisawa; Atsushi Kumanogoh; Hitoshi Kikutani
Journal:  Dev Biol       Date:  2008-06-30       Impact factor: 3.582

8.  Clonally dominant cardiomyocytes direct heart morphogenesis.

Authors:  Vikas Gupta; Kenneth D Poss
Journal:  Nature       Date:  2012-04-25       Impact factor: 49.962

9.  Moving domain computational fluid dynamics to interface with an embryonic model of cardiac morphogenesis.

Authors:  Juhyun Lee; Mahdi Esmaily Moghadam; Ethan Kung; Hung Cao; Tyler Beebe; Yury Miller; Beth L Roman; Ching-Ling Lien; Neil C Chi; Alison L Marsden; Tzung K Hsiai
Journal:  PLoS One       Date:  2013-08-23       Impact factor: 3.240

10.  Piezo1 and Gq/G11 promote endothelial inflammation depending on flow pattern and integrin activation.

Authors:  Julián Albarrán-Juárez; Andras Iring; ShengPeng Wang; Sayali Joseph; Myriam Grimm; Boris Strilic; Nina Wettschureck; Till F Althoff; Stefan Offermanns
Journal:  J Exp Med       Date:  2018-09-07       Impact factor: 14.307

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