Cardiac fibroblasts and mechanosensation in heart development, health and disease.

The term 'mechanosensation' describes the capacity of cells to translate mechanical stimuli into the coordinated regulation of intracellular signals, cellular function, gene expression and epigenetic programming. This capacity is related not only to the sensitivity of the cells to tissue motion, but...

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Publicado en:Nature Reviews Cardiology Vol. 20; no. 5; pp. 309 - 325
Autores principales: Pesce, Maurizio, Duda, Georg N., Forte, Giancarlo, Girao, Henrique, Raya, Angel, Roca-Cusachs, Pere, Sluijter, Joost P. G., Tschöpe, Carsten, Van Linthout, Sophie
Formato: review Journal Article
Publicado: Springer Nature May2023
Acceso en línea:Ver este registro en EBSCOhost
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        atl: Cardiac fibroblasts and mechanosensation in heart development, health and disease.
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          Pesce, Maurizio
          Duda, Georg N.
          Forte, Giancarlo
          Girao, Henrique
          Raya, Angel
          Roca-Cusachs, Pere
          Sluijter, Joost P. G.
          Tschöpe, Carsten
          Van Linthout, Sophie
        affil: Unità di Ingegneria Tissutale Cardiovascolare, Centro Cardiologico Monzino, IRCCS, Milan, Italy
      sug:
      ab: The term 'mechanosensation' describes the capacity of cells to translate mechanical stimuli into the coordinated regulation of intracellular signals, cellular function, gene expression and epigenetic programming. This capacity is related not only to the sensitivity of the cells to tissue motion, but also to the decryption of tissue geometric arrangement and mechanical properties. The cardiac stroma, composed of fibroblasts, has been historically considered a mechanically passive component of the heart. However, the latest research suggests that the mechanical functions of these cells are an active and necessary component of the developmental biology programme of the heart that is involved in myocardial growth and homeostasis, and a crucial determinant of cardiac repair and disease. In this Review, we discuss the general concept of cell mechanosensation and force generation as potent regulators in heart development and pathology, and describe the integration of mechanical and biohumoral pathways predisposing the heart to fibrosis and failure. Next, we address the use of 3D culture systems to integrate tissue mechanics to mimic cardiac remodelling. Finally, we highlight the potential of mechanotherapeutic strategies, including pharmacological treatment and device-mediated left ventricular unloading, to reverse remodelling in the failing heart.
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