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dc.contributor.authorLEWIS, Fen_US
dc.contributor.authorDeva Kumar, Sen_US
dc.contributor.authorEllison-Hughes, GMen_US
dc.date.accessioned2018-07-26T08:57:05Z
dc.date.available2017-08-30en_US
dc.date.issued2018-01-01en_US
dc.date.submitted2017-08-31T11:54:23.174Z
dc.identifier.issn1096-1186en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/42603
dc.description.abstractThe adult myocardium, including human, harbours a population of resident multi-potent cardiac stem cells (CSCs), which when stimulated under the right conditions can give rise to new cardiomyocytes and vasculature. Elucidation of the cellular and molecular mechanisms that govern CSC biology and their role in myocardial regeneration will allow the design and development of optimal therapeutic interventions. It is now evident that different growth factors and cytokines govern CSC survival, proliferation, migration and differentiation, as well as playing a role in activating cardiac repair mechanisms such as improving angiogenesis, cardiomyocyte survival and limiting fibrosis. This review article will summarize the evidence for a role of VEGF, NRG-1, IGF-1, HGF, EGF, FGF and TGF-β1 in modulating the repair and regeneration of cardiac tissue. It will also discuss the use of exosomes and exercise training as interventions to stimulate the endogenous repair and regenerative mechanisms in the damaged heart.en_US
dc.description.sponsorshipThis work was supported by grants from the British Heart Foundation (PG/06/045; PG 08/085), Marie Curie FP7 (PIRG02-GA-2007-224853), CARE-MI FP7-HEALTH-2009 (242038), Endostem FP7-HEALTH-2009 (241440).
dc.format.extent33 - 40en_US
dc.publisherElsevieren_US
dc.relation.ispartofPharmacological Researchen_US
dc.rights© 2017. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleNon-invasive strategies for stimulating endogenous repair and regenerative mechanisms in the damaged hearten_US
dc.typeArticle
dc.rights.holder© 2017 Elsevier Ltd. All rights reserved.
dc.identifier.doi10.1016/j.phrs.2017.08.016en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.publisher-urlhttps://doi.org/10.1016/j.phrs.2017.08.016en_US
pubs.volume127en_US
dcterms.dateAccepted2017-08-30en_US


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