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Immunologic properties of differentiated and undifferentiated mesenchymal stem cells derived from umbilical cord blood

The expression of immunogenic markers after differentiation of umbilical cord blood (UCB)-derived mesenchymal stem cells (MSC) has been poorly investigated and requires extensive in vitro and in vivo testing for clinical application. The expression of human leukocyte antigen (HLA) classes on UCB-der...

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Autores principales: Lee, Hyo-Jong, Kang, Kyung-Sun, Kang, Sun-Young, Kim, Hyung-Sik, Park, Se-Jin, Lee, Seung-Yong, Kim, Kwang-Dong, Lee, Hee-Chun, Park, Ji-Kwon, Paik, Won-Young, Lee, Lyon, Yeon, Seong-Chan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Veterinary Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037295/
https://www.ncbi.nlm.nih.gov/pubmed/26726028
http://dx.doi.org/10.4142/jvs.2016.17.3.289
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author Lee, Hyo-Jong
Kang, Kyung-Sun
Kang, Sun-Young
Kim, Hyung-Sik
Park, Se-Jin
Lee, Seung-Yong
Kim, Kwang-Dong
Lee, Hee-Chun
Park, Ji-Kwon
Paik, Won-Young
Lee, Lyon
Yeon, Seong-Chan
author_facet Lee, Hyo-Jong
Kang, Kyung-Sun
Kang, Sun-Young
Kim, Hyung-Sik
Park, Se-Jin
Lee, Seung-Yong
Kim, Kwang-Dong
Lee, Hee-Chun
Park, Ji-Kwon
Paik, Won-Young
Lee, Lyon
Yeon, Seong-Chan
author_sort Lee, Hyo-Jong
collection PubMed
description The expression of immunogenic markers after differentiation of umbilical cord blood (UCB)-derived mesenchymal stem cells (MSC) has been poorly investigated and requires extensive in vitro and in vivo testing for clinical application. The expression of human leukocyte antigen (HLA) classes on UCB-derived MSC was tested by Fluorescence-activated cell sorting analysis and immunocytochemical staining. The undifferentiated MSC were moderately positive for HLA-ABC, but almost completely negative for HLA-DR. The MSC differentiated to chondrocytes expressed neither HLA-ABC nor HLA-DR. The proliferation of MSC was not significantly affected by the allogeneic lymphocytes stimulated with concanavalin A. The responder lymphocytes showed no significant decrease in proliferation in the presence of the MSC, but the apoptosis rate of the lymphocytes was increased in the presence of MSC. Taken together, these findings indicate that UCB-derived MSC differentiated to chondrocytes expressed less HLA class I and no class II antigens. The MSC showed an immunomodulatory effect on the proliferation and apoptosis of allogeneic lymphocytes. These data suggest that the differentiated and undifferentiated allogeneic MSC derived from umbilical cord blood can be a useful candidate for allogeneic cell therapy and transplantation without a major risk of rejection.
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spelling pubmed-50372952016-09-29 Immunologic properties of differentiated and undifferentiated mesenchymal stem cells derived from umbilical cord blood Lee, Hyo-Jong Kang, Kyung-Sun Kang, Sun-Young Kim, Hyung-Sik Park, Se-Jin Lee, Seung-Yong Kim, Kwang-Dong Lee, Hee-Chun Park, Ji-Kwon Paik, Won-Young Lee, Lyon Yeon, Seong-Chan J Vet Sci Original Article The expression of immunogenic markers after differentiation of umbilical cord blood (UCB)-derived mesenchymal stem cells (MSC) has been poorly investigated and requires extensive in vitro and in vivo testing for clinical application. The expression of human leukocyte antigen (HLA) classes on UCB-derived MSC was tested by Fluorescence-activated cell sorting analysis and immunocytochemical staining. The undifferentiated MSC were moderately positive for HLA-ABC, but almost completely negative for HLA-DR. The MSC differentiated to chondrocytes expressed neither HLA-ABC nor HLA-DR. The proliferation of MSC was not significantly affected by the allogeneic lymphocytes stimulated with concanavalin A. The responder lymphocytes showed no significant decrease in proliferation in the presence of the MSC, but the apoptosis rate of the lymphocytes was increased in the presence of MSC. Taken together, these findings indicate that UCB-derived MSC differentiated to chondrocytes expressed less HLA class I and no class II antigens. The MSC showed an immunomodulatory effect on the proliferation and apoptosis of allogeneic lymphocytes. These data suggest that the differentiated and undifferentiated allogeneic MSC derived from umbilical cord blood can be a useful candidate for allogeneic cell therapy and transplantation without a major risk of rejection. The Korean Society of Veterinary Science 2016-09 2016-09-20 /pmc/articles/PMC5037295/ /pubmed/26726028 http://dx.doi.org/10.4142/jvs.2016.17.3.289 Text en © 2016 The Korean Society of Veterinary Science. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Hyo-Jong
Kang, Kyung-Sun
Kang, Sun-Young
Kim, Hyung-Sik
Park, Se-Jin
Lee, Seung-Yong
Kim, Kwang-Dong
Lee, Hee-Chun
Park, Ji-Kwon
Paik, Won-Young
Lee, Lyon
Yeon, Seong-Chan
Immunologic properties of differentiated and undifferentiated mesenchymal stem cells derived from umbilical cord blood
title Immunologic properties of differentiated and undifferentiated mesenchymal stem cells derived from umbilical cord blood
title_full Immunologic properties of differentiated and undifferentiated mesenchymal stem cells derived from umbilical cord blood
title_fullStr Immunologic properties of differentiated and undifferentiated mesenchymal stem cells derived from umbilical cord blood
title_full_unstemmed Immunologic properties of differentiated and undifferentiated mesenchymal stem cells derived from umbilical cord blood
title_short Immunologic properties of differentiated and undifferentiated mesenchymal stem cells derived from umbilical cord blood
title_sort immunologic properties of differentiated and undifferentiated mesenchymal stem cells derived from umbilical cord blood
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037295/
https://www.ncbi.nlm.nih.gov/pubmed/26726028
http://dx.doi.org/10.4142/jvs.2016.17.3.289
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