Message in a Bottle: Upgrading Cardiac Repair into Rejuvenation
Ischaemic cardiac disease is associated with a loss of cardiomyocytes and an intrinsic lack of myocardial renewal. Recent work has shown that the heart retains limited cardiomyocyte proliferation, which remains inefficient when facing pathological conditions. While broadly active in the neonatal mam...
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doaj-7781b49e8e014e61ad7d392c74ec44202020-11-25T02:28:41ZengMDPI AGCells2073-44092020-03-019372410.3390/cells9030724cells9030724Message in a Bottle: Upgrading Cardiac Repair into RejuvenationCarolina Balbi0Ambra Costa1Lucio Barile2Sveva Bollini3Laboratory of Cellular and Molecular Cardiology, Cardiocentro Ticino Foundation, 6900 Lugano, SwitzerlandRegenerative Medicine Laboratory, Dept. of Experimental Medicine (DIMES), University of Genova, 16132 Genova, ItalyLaboratory for Cardiovascular Theranostics, Cardiocentro Ticino Foundation, 6900 Lugano, SwitzerlandRegenerative Medicine Laboratory, Dept. of Experimental Medicine (DIMES), University of Genova, 16132 Genova, ItalyIschaemic cardiac disease is associated with a loss of cardiomyocytes and an intrinsic lack of myocardial renewal. Recent work has shown that the heart retains limited cardiomyocyte proliferation, which remains inefficient when facing pathological conditions. While broadly active in the neonatal mammalian heart, this mechanism becomes quiescent soon after birth, suggesting loss of regenerative potential with maturation into adulthood. A key question is whether this temporary regenerative window can be enhanced via appropriate stimulation and further extended. Recently the search for novel therapeutic approaches for heart disease has centred on stem cell biology. The “paracrine effect” has been proposed as a promising strategy to boost endogenous reparative and regenerative mechanisms from within the cardiac tissue by exploiting the modulatory potential of soluble stem cell-secreted factors. As such, growing interest has been specifically addressed towards stem/progenitor cell-secreted extracellular vesicles (EVs), which can be easily isolated in vitro from cell-conditioned medium. This review will provide a comprehensive overview of the current paradigm on cardiac repair and regeneration, with a specific focus on the role and mechanism(s) of paracrine action of EVs from cardiac stromal progenitors as compared to exogenous stem cells in order to discuss the optimal choice for future therapy. In addition, the challenges to overcoming translational EV biology from bench to bedside for future cardiac regenerative medicine will be discussed.https://www.mdpi.com/2073-4409/9/3/724paracrine effectextracellular vesiclesexosomescardiac repairangiogenesismyocardial renewalregeneration |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Carolina Balbi Ambra Costa Lucio Barile Sveva Bollini |
spellingShingle |
Carolina Balbi Ambra Costa Lucio Barile Sveva Bollini Message in a Bottle: Upgrading Cardiac Repair into Rejuvenation Cells paracrine effect extracellular vesicles exosomes cardiac repair angiogenesis myocardial renewal regeneration |
author_facet |
Carolina Balbi Ambra Costa Lucio Barile Sveva Bollini |
author_sort |
Carolina Balbi |
title |
Message in a Bottle: Upgrading Cardiac Repair into Rejuvenation |
title_short |
Message in a Bottle: Upgrading Cardiac Repair into Rejuvenation |
title_full |
Message in a Bottle: Upgrading Cardiac Repair into Rejuvenation |
title_fullStr |
Message in a Bottle: Upgrading Cardiac Repair into Rejuvenation |
title_full_unstemmed |
Message in a Bottle: Upgrading Cardiac Repair into Rejuvenation |
title_sort |
message in a bottle: upgrading cardiac repair into rejuvenation |
publisher |
MDPI AG |
series |
Cells |
issn |
2073-4409 |
publishDate |
2020-03-01 |
description |
Ischaemic cardiac disease is associated with a loss of cardiomyocytes and an intrinsic lack of myocardial renewal. Recent work has shown that the heart retains limited cardiomyocyte proliferation, which remains inefficient when facing pathological conditions. While broadly active in the neonatal mammalian heart, this mechanism becomes quiescent soon after birth, suggesting loss of regenerative potential with maturation into adulthood. A key question is whether this temporary regenerative window can be enhanced via appropriate stimulation and further extended. Recently the search for novel therapeutic approaches for heart disease has centred on stem cell biology. The “paracrine effect” has been proposed as a promising strategy to boost endogenous reparative and regenerative mechanisms from within the cardiac tissue by exploiting the modulatory potential of soluble stem cell-secreted factors. As such, growing interest has been specifically addressed towards stem/progenitor cell-secreted extracellular vesicles (EVs), which can be easily isolated in vitro from cell-conditioned medium. This review will provide a comprehensive overview of the current paradigm on cardiac repair and regeneration, with a specific focus on the role and mechanism(s) of paracrine action of EVs from cardiac stromal progenitors as compared to exogenous stem cells in order to discuss the optimal choice for future therapy. In addition, the challenges to overcoming translational EV biology from bench to bedside for future cardiac regenerative medicine will be discussed. |
topic |
paracrine effect extracellular vesicles exosomes cardiac repair angiogenesis myocardial renewal regeneration |
url |
https://www.mdpi.com/2073-4409/9/3/724 |
work_keys_str_mv |
AT carolinabalbi messageinabottleupgradingcardiacrepairintorejuvenation AT ambracosta messageinabottleupgradingcardiacrepairintorejuvenation AT luciobarile messageinabottleupgradingcardiacrepairintorejuvenation AT svevabollini messageinabottleupgradingcardiacrepairintorejuvenation |
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