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Feasibility and Efficiency of Human Bone Marrow Stromal Cell Culture with Allogeneic Platelet Lysate-Supplementation for Cell Therapy against Stroke

Currently, there is increasing interest in human bone marrow stromal cells (hBMSCs) as regeneration therapy against cerebral stroke. The aim of the present study was to evaluate the feasibility and validity of hBMSC cultures with allogeneic platelet lysates (PLs). Platelet concentrates (PC) were har...

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Autores principales: Tan, Chengbo, Shichinohe, Hideo, Wang, Zifeng, Hamauchi, Shuji, Abumiya, Takeo, Nakayama, Naoki, Kazumata, Ken, Ito, Tsuneo, Kudo, Kohsuke, Takamoto, Shigeru, Houkin, Kiyohiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093274/
https://www.ncbi.nlm.nih.gov/pubmed/27840648
http://dx.doi.org/10.1155/2016/6104780
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author Tan, Chengbo
Shichinohe, Hideo
Wang, Zifeng
Hamauchi, Shuji
Abumiya, Takeo
Nakayama, Naoki
Kazumata, Ken
Ito, Tsuneo
Kudo, Kohsuke
Takamoto, Shigeru
Houkin, Kiyohiro
author_facet Tan, Chengbo
Shichinohe, Hideo
Wang, Zifeng
Hamauchi, Shuji
Abumiya, Takeo
Nakayama, Naoki
Kazumata, Ken
Ito, Tsuneo
Kudo, Kohsuke
Takamoto, Shigeru
Houkin, Kiyohiro
author_sort Tan, Chengbo
collection PubMed
description Currently, there is increasing interest in human bone marrow stromal cells (hBMSCs) as regeneration therapy against cerebral stroke. The aim of the present study was to evaluate the feasibility and validity of hBMSC cultures with allogeneic platelet lysates (PLs). Platelet concentrates (PC) were harvested from healthy volunteers and made into single donor-derived PL (sPL). The PL mixtures (mPL) were made from three different sPL. Some growth factors and platelet cell surface antigens were detected by enzyme-linked immunosorbent assay (ELISA). The hBMSCs cultured with 10% PL were analyzed for their proliferative potential, surface markers, and karyotypes. The cells were incubated with superparamagnetic iron oxide (SPIO) agents and injected into a pig brain. MRI and histological analysis were performed. Consequently, nine lots of sPL and three mPL were prepared. ELISA analysis showed that PL contained adequate growth factors and a particle of platelet surface antigens. Cell proliferation capacity of PLs was equivalent to or higher than that of fetal calf serum (FCS). No contradiction in cell surface markers and no chromosomal aberrations were found. The MRI detected the distribution of SPIO-labeled hBMSCs in the pig brain. In summary, the hBMSCs cultured with allogeneic PL are suitable for cell therapy against stroke.
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spelling pubmed-50932742016-11-13 Feasibility and Efficiency of Human Bone Marrow Stromal Cell Culture with Allogeneic Platelet Lysate-Supplementation for Cell Therapy against Stroke Tan, Chengbo Shichinohe, Hideo Wang, Zifeng Hamauchi, Shuji Abumiya, Takeo Nakayama, Naoki Kazumata, Ken Ito, Tsuneo Kudo, Kohsuke Takamoto, Shigeru Houkin, Kiyohiro Stem Cells Int Research Article Currently, there is increasing interest in human bone marrow stromal cells (hBMSCs) as regeneration therapy against cerebral stroke. The aim of the present study was to evaluate the feasibility and validity of hBMSC cultures with allogeneic platelet lysates (PLs). Platelet concentrates (PC) were harvested from healthy volunteers and made into single donor-derived PL (sPL). The PL mixtures (mPL) were made from three different sPL. Some growth factors and platelet cell surface antigens were detected by enzyme-linked immunosorbent assay (ELISA). The hBMSCs cultured with 10% PL were analyzed for their proliferative potential, surface markers, and karyotypes. The cells were incubated with superparamagnetic iron oxide (SPIO) agents and injected into a pig brain. MRI and histological analysis were performed. Consequently, nine lots of sPL and three mPL were prepared. ELISA analysis showed that PL contained adequate growth factors and a particle of platelet surface antigens. Cell proliferation capacity of PLs was equivalent to or higher than that of fetal calf serum (FCS). No contradiction in cell surface markers and no chromosomal aberrations were found. The MRI detected the distribution of SPIO-labeled hBMSCs in the pig brain. In summary, the hBMSCs cultured with allogeneic PL are suitable for cell therapy against stroke. Hindawi Publishing Corporation 2016 2016-10-20 /pmc/articles/PMC5093274/ /pubmed/27840648 http://dx.doi.org/10.1155/2016/6104780 Text en Copyright © 2016 Chengbo Tan et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tan, Chengbo
Shichinohe, Hideo
Wang, Zifeng
Hamauchi, Shuji
Abumiya, Takeo
Nakayama, Naoki
Kazumata, Ken
Ito, Tsuneo
Kudo, Kohsuke
Takamoto, Shigeru
Houkin, Kiyohiro
Feasibility and Efficiency of Human Bone Marrow Stromal Cell Culture with Allogeneic Platelet Lysate-Supplementation for Cell Therapy against Stroke
title Feasibility and Efficiency of Human Bone Marrow Stromal Cell Culture with Allogeneic Platelet Lysate-Supplementation for Cell Therapy against Stroke
title_full Feasibility and Efficiency of Human Bone Marrow Stromal Cell Culture with Allogeneic Platelet Lysate-Supplementation for Cell Therapy against Stroke
title_fullStr Feasibility and Efficiency of Human Bone Marrow Stromal Cell Culture with Allogeneic Platelet Lysate-Supplementation for Cell Therapy against Stroke
title_full_unstemmed Feasibility and Efficiency of Human Bone Marrow Stromal Cell Culture with Allogeneic Platelet Lysate-Supplementation for Cell Therapy against Stroke
title_short Feasibility and Efficiency of Human Bone Marrow Stromal Cell Culture with Allogeneic Platelet Lysate-Supplementation for Cell Therapy against Stroke
title_sort feasibility and efficiency of human bone marrow stromal cell culture with allogeneic platelet lysate-supplementation for cell therapy against stroke
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093274/
https://www.ncbi.nlm.nih.gov/pubmed/27840648
http://dx.doi.org/10.1155/2016/6104780
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