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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Autores principales: Fernández Vallone, V.B., Romaniuk, M.A., Choi, H., Labovsky, V., Otaegui, J., Chasseing, N.A.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_03014681_v85_n1-2_p1_FernandezVallone
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spelling todo:paper_03014681_v85_n1-2_p1_FernandezVallone2023-10-03T15:18:22Z Mesenchymal stem cells and their use in therapy: What has been achieved? Fernández Vallone, V.B. Romaniuk, M.A. Choi, H. Labovsky, V. Otaegui, J. Chasseing, N.A. Bone marrow Mesenchymal stem cells Plasticity 5' nucleotidase CD11b antigen CD14 antigen CD19 antigen CD34 antigen CD45 antigen CD79a antigen endoglin HLA DR antigen interleukin 10 interleukin 4 Thy 1 antigen toll like receptor 3 toll like receptor 4 tumor necrosis factor alpha acute lung injury adipocyte adipose tissue antigen expression bone marrow cartilage cell cell adhesion cell differentiation cell expansion cell isolation cell lineage cell renewal cell transdifferentiation cerebrovascular accident Crohn disease culture medium cytokine production diabetes mellitus hematopoiesis human immunogenicity immunological tolerance immunomodulation immunostimulation in vitro study kidney injury medical society mesenchymal stem cell mesenchymal stem cell transplantation nonhuman osteoblast osteogenesis imperfecta Parkinson disease priority journal review risk assessment risk benefit analysis spinal cord injury tissue regeneration tumor growth Cell Differentiation Humans Mesenchymal Stem Cell Transplantation Mesenchymal Stromal Cells Bovinae 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. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03014681_v85_n1-2_p1_FernandezVallone
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Bone marrow
Mesenchymal stem cells
Plasticity
5' nucleotidase
CD11b antigen
CD14 antigen
CD19 antigen
CD34 antigen
CD45 antigen
CD79a antigen
endoglin
HLA DR antigen
interleukin 10
interleukin 4
Thy 1 antigen
toll like receptor 3
toll like receptor 4
tumor necrosis factor alpha
acute lung injury
adipocyte
adipose tissue
antigen expression
bone marrow
cartilage cell
cell adhesion
cell differentiation
cell expansion
cell isolation
cell lineage
cell renewal
cell transdifferentiation
cerebrovascular accident
Crohn disease
culture medium
cytokine production
diabetes mellitus
hematopoiesis
human
immunogenicity
immunological tolerance
immunomodulation
immunostimulation
in vitro study
kidney injury
medical society
mesenchymal stem cell
mesenchymal stem cell transplantation
nonhuman
osteoblast
osteogenesis imperfecta
Parkinson disease
priority journal
review
risk assessment
risk benefit analysis
spinal cord injury
tissue regeneration
tumor growth
Cell Differentiation
Humans
Mesenchymal Stem Cell Transplantation
Mesenchymal Stromal Cells
Bovinae
spellingShingle Bone marrow
Mesenchymal stem cells
Plasticity
5' nucleotidase
CD11b antigen
CD14 antigen
CD19 antigen
CD34 antigen
CD45 antigen
CD79a antigen
endoglin
HLA DR antigen
interleukin 10
interleukin 4
Thy 1 antigen
toll like receptor 3
toll like receptor 4
tumor necrosis factor alpha
acute lung injury
adipocyte
adipose tissue
antigen expression
bone marrow
cartilage cell
cell adhesion
cell differentiation
cell expansion
cell isolation
cell lineage
cell renewal
cell transdifferentiation
cerebrovascular accident
Crohn disease
culture medium
cytokine production
diabetes mellitus
hematopoiesis
human
immunogenicity
immunological tolerance
immunomodulation
immunostimulation
in vitro study
kidney injury
medical society
mesenchymal stem cell
mesenchymal stem cell transplantation
nonhuman
osteoblast
osteogenesis imperfecta
Parkinson disease
priority journal
review
risk assessment
risk benefit analysis
spinal cord injury
tissue regeneration
tumor growth
Cell Differentiation
Humans
Mesenchymal Stem Cell Transplantation
Mesenchymal Stromal Cells
Bovinae
Fernández Vallone, V.B.
Romaniuk, M.A.
Choi, H.
Labovsky, V.
Otaegui, J.
Chasseing, N.A.
Mesenchymal stem cells and their use in therapy: What has been achieved?
topic_facet Bone marrow
Mesenchymal stem cells
Plasticity
5' nucleotidase
CD11b antigen
CD14 antigen
CD19 antigen
CD34 antigen
CD45 antigen
CD79a antigen
endoglin
HLA DR antigen
interleukin 10
interleukin 4
Thy 1 antigen
toll like receptor 3
toll like receptor 4
tumor necrosis factor alpha
acute lung injury
adipocyte
adipose tissue
antigen expression
bone marrow
cartilage cell
cell adhesion
cell differentiation
cell expansion
cell isolation
cell lineage
cell renewal
cell transdifferentiation
cerebrovascular accident
Crohn disease
culture medium
cytokine production
diabetes mellitus
hematopoiesis
human
immunogenicity
immunological tolerance
immunomodulation
immunostimulation
in vitro study
kidney injury
medical society
mesenchymal stem cell
mesenchymal stem cell transplantation
nonhuman
osteoblast
osteogenesis imperfecta
Parkinson disease
priority journal
review
risk assessment
risk benefit analysis
spinal cord injury
tissue regeneration
tumor growth
Cell Differentiation
Humans
Mesenchymal Stem Cell Transplantation
Mesenchymal Stromal Cells
Bovinae
description 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.
format JOUR
author Fernández Vallone, V.B.
Romaniuk, M.A.
Choi, H.
Labovsky, V.
Otaegui, J.
Chasseing, N.A.
author_facet Fernández Vallone, V.B.
Romaniuk, M.A.
Choi, H.
Labovsky, V.
Otaegui, J.
Chasseing, N.A.
author_sort Fernández Vallone, V.B.
title Mesenchymal stem cells and their use in therapy: What has been achieved?
title_short Mesenchymal stem cells and their use in therapy: What has been achieved?
title_full Mesenchymal stem cells and their use in therapy: What has been achieved?
title_fullStr Mesenchymal stem cells and their use in therapy: What has been achieved?
title_full_unstemmed Mesenchymal stem cells and their use in therapy: What has been achieved?
title_sort mesenchymal stem cells and their use in therapy: what has been achieved?
url http://hdl.handle.net/20.500.12110/paper_03014681_v85_n1-2_p1_FernandezVallone
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AT choih mesenchymalstemcellsandtheiruseintherapywhathasbeenachieved
AT labovskyv mesenchymalstemcellsandtheiruseintherapywhathasbeenachieved
AT otaeguij mesenchymalstemcellsandtheiruseintherapywhathasbeenachieved
AT chasseingna mesenchymalstemcellsandtheiruseintherapywhathasbeenachieved
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