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dc.contributor.author
Simerman, Ariel A.
dc.contributor.author
Perone, Marcelo Javier
dc.contributor.author
Gimeno, Maria Laura
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Dumesic, Daniel A.
dc.contributor.author
Chazenblak, Gregorio D.
dc.date.available
2017-02-01T20:09:10Z
dc.date.issued
2014-03
dc.identifier.citation
Simerman, Ariel A.; Perone, Marcelo Javier; Gimeno, Maria Laura; Dumesic, Daniel A.; Chazenblak, Gregorio D.; A Mystery Unraveled: Non-tumorigenic pluripotent stem cells in human adult tissues; Informa Healthcare; Expert Opinion On Biological Therapy; 14; 7; 3-2014; 917-929
dc.identifier.issn
1471-2598
dc.identifier.uri
http://hdl.handle.net/11336/12308
dc.description.abstract
Embryonic stem cells and induced pluripotent stem cells have emerged as the gold standard of pluripotent stem cells and the class of 10 stem cell with the highest potential for contribution to regenerative and therapeutic application; however, their translational use is often impeded by teratoma formation, commonly associated with pluripotency. We discuss a population of nontumorigenic pluripotent stem cells, termed Multilineage Differentiating Stress Enduring (Muse) cells, which offer an innovative and 15 exciting avenue of exploration for the potential treatment of various human diseases. Areas covered: This review discusses the origin of Muse cells, describes in detail their various unique characteristics, and considers future avenues of their application and investigation with respect to what is currently known 20 of adult pluripotent stem cells in scientific literature. We begin by defining cell potency, then discussing both mesenchymal and various reported populations of pluripotent stem cells, and finally, delving into Muse cells and what sets them apart from their contemporaries. Expert opinion: Muse cells derived from adipose tissue (Muse-AT) are 25 efficiently, routinely and painlessly isolated from human lipoaspirate material, exhibit tripoblastic differentiation both spontaneously and under media-specific induction, and do not form teratomas. We describe qualities specific to Muse-ATcells and their potential impact on the field of regenerative medicine and cell therapy.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Informa Healthcare
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Human Pluripotent Stem Cells
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Muse Cells
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Nontumorigenic
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Regenerative Medicine
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Fisiología
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Medicina Básica
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CIENCIAS MÉDICAS Y DE LA SALUD
dc.title
A Mystery Unraveled: Non-tumorigenic pluripotent stem cells in human adult tissues
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2016-12-12T20:46:58Z
dc.journal.volume
14
dc.journal.number
7
dc.journal.pagination
917-929
dc.journal.pais
Reino Unido
dc.journal.ciudad
London
dc.description.fil
Fil: Simerman, Ariel A.. University of California; Estados Unidos
dc.description.fil
Fil: Perone, Marcelo Javier. University of California; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigación en Biomedicina de Buenos Aires; Argentina
dc.description.fil
Fil: Gimeno, Maria Laura. University of California; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigación en Biomedicina de Buenos Aires; Argentina
dc.description.fil
Fil: Dumesic, Daniel A.. University of California; Estados Unidos
dc.description.fil
Fil: Chazenblak, Gregorio D.. University of California; Estados Unidos
dc.journal.title
Expert Opinion On Biological Therapy
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.tandfonline.com/doi/abs/10.1517/14712598.2014.900538?journalCode=iebt20
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1517/14712598.2014.900538
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4100978/
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