Mesenchymal stem cells and their use in therapy: What has been achieved?

The considerable therapeutic potential of human multipotent mesenchymal stromal cells or mesenchymal stem cells (MSCs) has generated increasing interest in a wide variety of biomedical disciplines. Nevertheless, researchers report studies on MSCs using different methods of isolation and expansion, a...

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Autor principal: Fernández Vallone, V.B
Otros Autores: Romaniuk, M.A, Choi, H., Labovsky, V., Otaegui, J., Chasseing, N.A
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2013
Acceso en línea:Registro en Scopus
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245 1 0 |a Mesenchymal stem cells and their use in therapy: What has been achieved? 
260 |c 2013 
270 1 0 |m Chasseing, N.A.2490 Vuelta de Obligado, Ciudad Autonoma de Buenos Aires (1428), Buenos Aires, Argentina; email: achasseing@ibyme.conicet.gov.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a The considerable therapeutic potential of human multipotent mesenchymal stromal cells or mesenchymal stem cells (MSCs) has generated increasing interest in a wide variety of biomedical disciplines. Nevertheless, researchers report studies on MSCs using different methods of isolation and expansion, as well as different approaches to characterize them; therefore, it is increasingly difficult to compare and contrast study outcomes. To begin to address this issue, the Mesenchymal and Tissue Stem Cell Committee of the International Society for Cellular Therapy proposed minimal criteria to define human MSCs. First, MSCs must be plastic-adherent when maintained in standard culture conditions (α minimal essential medium plus 20% fetal bovine serum). Second, MSCs must express CD105, CD73 and CD90, and MSCs must lack expression of CD45, CD34, CD14 or CD11b, CD79α or CD19 and HLA-DR surface molecules. Third, MSCs must differentiate into osteoblasts, adipocytes and chondroblasts in vitro. MSCs are isolated from many adult tissues, in particular from bone marrow and adipose tissue. Along with their capacity to differentiate and transdifferentiate into cells of different lineages, these cells have also generated great interest for their ability to display immunomodulatory capacities. Indeed, a major breakthrough was the finding that MSCs are able to induce peripheral tolerance, suggesting that they may be used as therapeutic tools in immune-mediated disorders. Although no significant adverse events have been reported in clinical trials to date, all interventional therapies have some inherent risks. Potential risks for undesirable events, such as tumor development, that might occur while using these stem cells for therapy must be taken into account and contrasted against the potential benefits to patients. © 2012 International Society of Differentiation.  |l eng 
593 |a Experimental Biology and Medicine Institute, CONICET, Buenos Aires, Argentina 
593 |a Thrombosis I Laboratory, Hematological Research Institute, National Academy of Medicine, CONICET, Buenos Aires, Argentina 
593 |a Institute for Regenerative Medicine, Texas A and M Health Sciences Center, Temple, TX, United States 
593 |a 2490 Vuelta de Obligado, Ciudad Autonoma de Buenos Aires (1428), Buenos Aires, Argentina 
593 |a 3092 Las Heras Avenue, Ciudad Autonoma de Buenos Aires (1425), Buenos Aires, Argentina 
593 |a 5701 Airport Road, Module C., Temple, TX 76502, United States 
690 1 0 |a BONE MARROW 
690 1 0 |a MESENCHYMAL STEM CELLS 
690 1 0 |a PLASTICITY 
690 1 0 |a 5' NUCLEOTIDASE 
690 1 0 |a CD11B ANTIGEN 
690 1 0 |a CD14 ANTIGEN 
690 1 0 |a CD19 ANTIGEN 
690 1 0 |a CD34 ANTIGEN 
690 1 0 |a CD45 ANTIGEN 
690 1 0 |a CD79A ANTIGEN 
690 1 0 |a ENDOGLIN 
690 1 0 |a HLA DR ANTIGEN 
690 1 0 |a INTERLEUKIN 10 
690 1 0 |a INTERLEUKIN 4 
690 1 0 |a THY 1 ANTIGEN 
690 1 0 |a TOLL LIKE RECEPTOR 3 
690 1 0 |a TOLL LIKE RECEPTOR 4 
690 1 0 |a TUMOR NECROSIS FACTOR ALPHA 
690 1 0 |a ACUTE LUNG INJURY 
690 1 0 |a ADIPOCYTE 
690 1 0 |a ADIPOSE TISSUE 
690 1 0 |a ANTIGEN EXPRESSION 
690 1 0 |a BONE MARROW 
690 1 0 |a CARTILAGE CELL 
690 1 0 |a CELL ADHESION 
690 1 0 |a CELL DIFFERENTIATION 
690 1 0 |a CELL EXPANSION 
690 1 0 |a CELL ISOLATION 
690 1 0 |a CELL LINEAGE 
690 1 0 |a CELL RENEWAL 
690 1 0 |a CELL TRANSDIFFERENTIATION 
690 1 0 |a CEREBROVASCULAR ACCIDENT 
690 1 0 |a CROHN DISEASE 
690 1 0 |a CULTURE MEDIUM 
690 1 0 |a CYTOKINE PRODUCTION 
690 1 0 |a DIABETES MELLITUS 
690 1 0 |a HEMATOPOIESIS 
690 1 0 |a HUMAN 
690 1 0 |a IMMUNOGENICITY 
690 1 0 |a IMMUNOLOGICAL TOLERANCE 
690 1 0 |a IMMUNOMODULATION 
690 1 0 |a IMMUNOSTIMULATION 
690 1 0 |a IN VITRO STUDY 
690 1 0 |a KIDNEY INJURY 
690 1 0 |a MEDICAL SOCIETY 
690 1 0 |a MESENCHYMAL STEM CELL 
690 1 0 |a MESENCHYMAL STEM CELL TRANSPLANTATION 
690 1 0 |a NONHUMAN 
690 1 0 |a OSTEOBLAST 
690 1 0 |a OSTEOGENESIS IMPERFECTA 
690 1 0 |a PARKINSON DISEASE 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a REVIEW 
690 1 0 |a RISK ASSESSMENT 
690 1 0 |a RISK BENEFIT ANALYSIS 
690 1 0 |a SPINAL CORD INJURY 
690 1 0 |a TISSUE REGENERATION 
690 1 0 |a TUMOR GROWTH 
690 1 0 |a CELL DIFFERENTIATION 
690 1 0 |a HUMANS 
690 1 0 |a MESENCHYMAL STEM CELL TRANSPLANTATION 
690 1 0 |a MESENCHYMAL STROMAL CELLS 
690 1 0 |a BOVINAE 
700 1 |a Romaniuk, M.A. 
700 1 |a Choi, H. 
700 1 |a Labovsky, V. 
700 1 |a Otaegui, J. 
700 1 |a Chasseing, N.A. 
773 0 |d 2013  |g v. 85  |h pp. 1-10  |k n. 1-2  |p Differentiation  |x 03014681  |t Differentiation 
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