Tailored generation of insulin producing cells from canine mesenchymal stem cells derived from bone marrow and adipose tissue
Abstract The trend of regenerative therapy for diabetes in human and veterinary practices has conceptually been proven according to the Edmonton protocol and animal models. Establishing an alternative insulin-producing cell (IPC) resource for further clinical application is a challenging task. This...
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Nature Portfolio
2021
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oai:doaj.org-article:b5b1b7182f6f4709893ea53f8f2459582021-12-02T17:52:32ZTailored generation of insulin producing cells from canine mesenchymal stem cells derived from bone marrow and adipose tissue10.1038/s41598-021-91774-32045-2322https://doaj.org/article/b5b1b7182f6f4709893ea53f8f2459582021-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-91774-3https://doaj.org/toc/2045-2322Abstract The trend of regenerative therapy for diabetes in human and veterinary practices has conceptually been proven according to the Edmonton protocol and animal models. Establishing an alternative insulin-producing cell (IPC) resource for further clinical application is a challenging task. This study investigated IPC generation from two practical canine mesenchymal stem cells (cMSCs), canine bone marrow-derived MSCs (cBM-MSCs) and canine adipose-derived MSCs (cAD-MSCs). The results illustrated that cBM-MSCs and cAD-MSCs contain distinct pancreatic differentiation potential and require the tailor-made induction protocols. The effective generation of cBM-MSC-derived IPCs needs the integration of genetic and microenvironment manipulation using a hanging-drop culture of PDX1-transfected cBM-MSCs under a three-step pancreatic induction protocol. However, this protocol is resource- and time-consuming. Another study on cAD-MSC-derived IPC generation found that IPC colonies could be obtained by a low attachment culture under the three-step induction protocol. Further, Notch signaling inhibition during pancreatic endoderm/progenitor induction yielded IPC colonies through the trend of glucose-responsive C-peptide secretion. Thus, this study showed that IPCs could be obtained from cBM-MSCs and cAD-MSCs through different induction techniques. Also, further signaling manipulation studies should be conducted to maximize the protocol’s efficiency.Watchareewan RodprasertSirirat NantavisaiKoranis PathanachaiPrasit PavasantThanaphum OsathanonChenphop SawangmakeNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-17 (2021) |
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Medicine R Science Q Watchareewan Rodprasert Sirirat Nantavisai Koranis Pathanachai Prasit Pavasant Thanaphum Osathanon Chenphop Sawangmake Tailored generation of insulin producing cells from canine mesenchymal stem cells derived from bone marrow and adipose tissue |
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Abstract The trend of regenerative therapy for diabetes in human and veterinary practices has conceptually been proven according to the Edmonton protocol and animal models. Establishing an alternative insulin-producing cell (IPC) resource for further clinical application is a challenging task. This study investigated IPC generation from two practical canine mesenchymal stem cells (cMSCs), canine bone marrow-derived MSCs (cBM-MSCs) and canine adipose-derived MSCs (cAD-MSCs). The results illustrated that cBM-MSCs and cAD-MSCs contain distinct pancreatic differentiation potential and require the tailor-made induction protocols. The effective generation of cBM-MSC-derived IPCs needs the integration of genetic and microenvironment manipulation using a hanging-drop culture of PDX1-transfected cBM-MSCs under a three-step pancreatic induction protocol. However, this protocol is resource- and time-consuming. Another study on cAD-MSC-derived IPC generation found that IPC colonies could be obtained by a low attachment culture under the three-step induction protocol. Further, Notch signaling inhibition during pancreatic endoderm/progenitor induction yielded IPC colonies through the trend of glucose-responsive C-peptide secretion. Thus, this study showed that IPCs could be obtained from cBM-MSCs and cAD-MSCs through different induction techniques. Also, further signaling manipulation studies should be conducted to maximize the protocol’s efficiency. |
format |
article |
author |
Watchareewan Rodprasert Sirirat Nantavisai Koranis Pathanachai Prasit Pavasant Thanaphum Osathanon Chenphop Sawangmake |
author_facet |
Watchareewan Rodprasert Sirirat Nantavisai Koranis Pathanachai Prasit Pavasant Thanaphum Osathanon Chenphop Sawangmake |
author_sort |
Watchareewan Rodprasert |
title |
Tailored generation of insulin producing cells from canine mesenchymal stem cells derived from bone marrow and adipose tissue |
title_short |
Tailored generation of insulin producing cells from canine mesenchymal stem cells derived from bone marrow and adipose tissue |
title_full |
Tailored generation of insulin producing cells from canine mesenchymal stem cells derived from bone marrow and adipose tissue |
title_fullStr |
Tailored generation of insulin producing cells from canine mesenchymal stem cells derived from bone marrow and adipose tissue |
title_full_unstemmed |
Tailored generation of insulin producing cells from canine mesenchymal stem cells derived from bone marrow and adipose tissue |
title_sort |
tailored generation of insulin producing cells from canine mesenchymal stem cells derived from bone marrow and adipose tissue |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/b5b1b7182f6f4709893ea53f8f245958 |
work_keys_str_mv |
AT watchareewanrodprasert tailoredgenerationofinsulinproducingcellsfromcaninemesenchymalstemcellsderivedfrombonemarrowandadiposetissue AT siriratnantavisai tailoredgenerationofinsulinproducingcellsfromcaninemesenchymalstemcellsderivedfrombonemarrowandadiposetissue AT koranispathanachai tailoredgenerationofinsulinproducingcellsfromcaninemesenchymalstemcellsderivedfrombonemarrowandadiposetissue AT prasitpavasant tailoredgenerationofinsulinproducingcellsfromcaninemesenchymalstemcellsderivedfrombonemarrowandadiposetissue AT thanaphumosathanon tailoredgenerationofinsulinproducingcellsfromcaninemesenchymalstemcellsderivedfrombonemarrowandadiposetissue AT chenphopsawangmake tailoredgenerationofinsulinproducingcellsfromcaninemesenchymalstemcellsderivedfrombonemarrowandadiposetissue |
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