The march of pluripotent stem cells in cardiovascular regenerative medicine

dc.contributor.authorAbou-Saleh, Haissam
dc.contributor.authorZouein, Fouad A.
dc.contributor.authorEl-Yazbi, Ahmed F.
dc.contributor.authorSanoudou, Despina
dc.contributor.authorRaynaud, Christophe Michel
dc.contributor.authorRao, Christopher
dc.contributor.authorPintus, Gianfranco
dc.contributor.authorDehaini, Hassan
dc.contributor.authorEid, Ali H.
dc.contributor.departmentPharmacology and Toxicology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:39:31Z
dc.date.available2025-01-24T11:39:31Z
dc.date.issued2018
dc.description.abstractCardiovascular disease (CVD) continues to be the leading cause of global morbidity and mortality. Heart failure remains a major contributor to this mortality. Despite major therapeutic advances over the past decades, a better understanding of molecular and cellular mechanisms of CVD as well as improved therapeutic strategies for the management or treatment of heart failure are increasingly needed. Loss of myocardium is a major driver of heart failure. An attractive approach that appears to provide promising results in reducing cardiac degeneration is stem cell therapy (SCT). In this review, we describe different types of stem cells, including embryonic and adult stem cells, and we provide a detailed discussion of the properties of induced pluripotent stem cells (iPSCs). We also present and critically discuss the key methods used for converting somatic cells to pluripotent cells and iPSCs to cardiomyocytes (CMs), along with their advantages and limitations. Integrating and non-integrating reprogramming methods as well as characterization of iPSCs and iPSC-derived CMs are discussed. Furthermore, we critically present various methods of differentiating iPSCs to CMs. The value of iPSC-CMs in regenerative medicine as well as myocardial disease modeling and cardiac regeneration are emphasized. © 2018 The Author(s).
dc.identifier.doihttps://doi.org/10.1186/s13287-018-0947-5
dc.identifier.eid2-s2.0-85050742962
dc.identifier.pmid30053890
dc.identifier.urihttp://hdl.handle.net/10938/29264
dc.language.isoen
dc.publisherBioMed Central Ltd.
dc.relation.ispartofStem Cell Research and Therapy
dc.sourceScopus
dc.subjectCardiomyocytes
dc.subjectCardiovascular disease
dc.subjectHeart failure
dc.subjectIpscs
dc.subjectRegenerative medicine
dc.subjectStem cell therapy
dc.subjectCardiovascular diseases
dc.subjectCell differentiation
dc.subjectCell- and tissue-based therapy
dc.subjectHumans
dc.subjectMyocytes, cardiac
dc.subjectPluripotent stem cells
dc.subjectCd34 antigen
dc.subjectCre recombinase
dc.subjectGrowth factor
dc.subjectMessenger rna
dc.subjectMinicircle dna
dc.subjectPlasmid dna
dc.subjectTranscription factor nanog
dc.subjectTransposase
dc.subjectZinc finger nuclease
dc.subjectAdipose derived stem cell
dc.subjectAdult stem cell
dc.subjectCardiac stem cell
dc.subjectCardiomyopathy
dc.subjectCell nucleus transplantation
dc.subjectCell reprogramming technique
dc.subjectCoculture
dc.subjectDrug screening
dc.subjectEmbryoid body
dc.subjectEmbryonic stem cell
dc.subjectFibroblast
dc.subjectHeart pacing
dc.subjectHuman
dc.subjectInduced pluripotent stem cell
dc.subjectKeratinocyte
dc.subjectLiquid chromatography-mass spectrometry
dc.subjectLive cell imaging
dc.subjectLong qt syndrome
dc.subjectLoxp site
dc.subjectMelanocyte
dc.subjectMultipotent stem cell
dc.subjectMyocardial disease
dc.subjectNeural stem cell
dc.subjectNonhuman
dc.subjectPluripotent stem cell
dc.subjectPriority journal
dc.subjectReview
dc.subjectStem cell transplantation
dc.subjectTissue regeneration
dc.subjectTransposon
dc.subjectUmbilical cord blood
dc.subjectVirus dna cell dna interaction
dc.subjectBiological therapy
dc.subjectCardiac muscle cell
dc.subjectGenetics
dc.subjectMetabolism
dc.subjectProcedures
dc.titleThe march of pluripotent stem cells in cardiovascular regenerative medicine
dc.typeReview

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
2018-8122.pdf
Size:
2.54 MB
Format:
Adobe Portable Document Format