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Mesenchymal stroma cells in peritoneal dialysis effluents from patients

Mesenchymal stroma cells (MSCs) have potential as an emerging cell therapy for treating many different diseases, but discovery of the practical sources of MSCs is needed for the large-scale clinical application of this therapy. This study was to identify MSCs in peritoneal dialysis (PD) effluents th...

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Autores principales: Liu, Bin, Guan, Qiunong, Li, Jing, da Roza, Gerald, Wang, Hao, Du, Caigan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357254/
https://www.ncbi.nlm.nih.gov/pubmed/28058621
http://dx.doi.org/10.1007/s13577-016-0155-5
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author Liu, Bin
Guan, Qiunong
Li, Jing
da Roza, Gerald
Wang, Hao
Du, Caigan
author_facet Liu, Bin
Guan, Qiunong
Li, Jing
da Roza, Gerald
Wang, Hao
Du, Caigan
author_sort Liu, Bin
collection PubMed
description Mesenchymal stroma cells (MSCs) have potential as an emerging cell therapy for treating many different diseases, but discovery of the practical sources of MSCs is needed for the large-scale clinical application of this therapy. This study was to identify MSCs in peritoneal dialysis (PD) effluents that were discarded after PD. The effluents were collected from patients who were on the dialysis for less than 1 month. Adherent cells from the effluents were isolated by incubation in serum-containing medium in plastic culture dishes. Cell surface markers were determined by a flow cytometric analysis, and the in vitro differentiation to chondrocytes, osteocytes or adipocytes was confirmed by staining with a specific dye. After four passages, these isolated cells displayed the typical morphology of mesenchymal cells in traditional 2-D cultures, and were grown to form spherical colonies in 3-D collagen cultures. Flow cytometric analysis revealed that the unsorted cells from all of seven patient samples showed robust expression of typical mesenchymal marker CD29, CD44, CD73, CD90 and CD166, and the absence of CD34, CD79a, CD105, CD271, SSEA-4, Stro-1 and HLA-DR. In differentiation assays, these cells were induced in vitro to chondrocytes, osteocytes or adipocytes. In conclusion, this preliminary study suggests the presence of MSCs in the “discarded” PD effluents. Further characterization of the phenotypes of these MSCs and evaluation of their therapeutic potential, particularly for the prevention of PD failure, are needed.
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spelling pubmed-53572542017-03-30 Mesenchymal stroma cells in peritoneal dialysis effluents from patients Liu, Bin Guan, Qiunong Li, Jing da Roza, Gerald Wang, Hao Du, Caigan Hum Cell Rapid Communication Mesenchymal stroma cells (MSCs) have potential as an emerging cell therapy for treating many different diseases, but discovery of the practical sources of MSCs is needed for the large-scale clinical application of this therapy. This study was to identify MSCs in peritoneal dialysis (PD) effluents that were discarded after PD. The effluents were collected from patients who were on the dialysis for less than 1 month. Adherent cells from the effluents were isolated by incubation in serum-containing medium in plastic culture dishes. Cell surface markers were determined by a flow cytometric analysis, and the in vitro differentiation to chondrocytes, osteocytes or adipocytes was confirmed by staining with a specific dye. After four passages, these isolated cells displayed the typical morphology of mesenchymal cells in traditional 2-D cultures, and were grown to form spherical colonies in 3-D collagen cultures. Flow cytometric analysis revealed that the unsorted cells from all of seven patient samples showed robust expression of typical mesenchymal marker CD29, CD44, CD73, CD90 and CD166, and the absence of CD34, CD79a, CD105, CD271, SSEA-4, Stro-1 and HLA-DR. In differentiation assays, these cells were induced in vitro to chondrocytes, osteocytes or adipocytes. In conclusion, this preliminary study suggests the presence of MSCs in the “discarded” PD effluents. Further characterization of the phenotypes of these MSCs and evaluation of their therapeutic potential, particularly for the prevention of PD failure, are needed. Springer Japan 2017-01-05 2017 /pmc/articles/PMC5357254/ /pubmed/28058621 http://dx.doi.org/10.1007/s13577-016-0155-5 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Rapid Communication
Liu, Bin
Guan, Qiunong
Li, Jing
da Roza, Gerald
Wang, Hao
Du, Caigan
Mesenchymal stroma cells in peritoneal dialysis effluents from patients
title Mesenchymal stroma cells in peritoneal dialysis effluents from patients
title_full Mesenchymal stroma cells in peritoneal dialysis effluents from patients
title_fullStr Mesenchymal stroma cells in peritoneal dialysis effluents from patients
title_full_unstemmed Mesenchymal stroma cells in peritoneal dialysis effluents from patients
title_short Mesenchymal stroma cells in peritoneal dialysis effluents from patients
title_sort mesenchymal stroma cells in peritoneal dialysis effluents from patients
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357254/
https://www.ncbi.nlm.nih.gov/pubmed/28058621
http://dx.doi.org/10.1007/s13577-016-0155-5
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