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Comparison of osteoclast differentiation protocols from human induced pluripotent stem cells of different tissue origins
BACKGROUND: Ever since their discovery, induced pluripotent stem cells (iPSCs) have been extensively differentiated into a large variety of cell types. However, a limited amount of work has been dedicated to differentiating iPSCs into osteoclasts. While several differentiation protocols have been pu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10631132/ https://www.ncbi.nlm.nih.gov/pubmed/37936199 http://dx.doi.org/10.1186/s13287-023-03547-6 |
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author | Blümke, Alexander Ijeoma, Erica Simon, Jessica Wellington, Rachel Purwaningrum, Medania Doulatov, Sergei Leber, Elizabeth Scatena, Marta Giachelli, Cecilia M. |
author_facet | Blümke, Alexander Ijeoma, Erica Simon, Jessica Wellington, Rachel Purwaningrum, Medania Doulatov, Sergei Leber, Elizabeth Scatena, Marta Giachelli, Cecilia M. |
author_sort | Blümke, Alexander |
collection | PubMed |
description | BACKGROUND: Ever since their discovery, induced pluripotent stem cells (iPSCs) have been extensively differentiated into a large variety of cell types. However, a limited amount of work has been dedicated to differentiating iPSCs into osteoclasts. While several differentiation protocols have been published, it remains unclear which protocols or differentiation methods are preferable regarding the differentiation of osteoclasts. METHODS: In this study, we compared the osteoclastogenesis capacity of a peripheral blood mononuclear cell (PBMC)-derived iPSC line to a fibroblast-derived iPSC line in conjunction with either embryoid body-based or monolayer-based differentiation strategies. Both cell lines and differentiation protocols were investigated regarding their ability to generate osteoclasts and their inherent robustness and ease of use. The ability of both cell lines to remain undifferentiated while propagating using a feeder-free system was assessed using alkaline phosphatase staining. This was followed by evaluating mesodermal differentiation and the characterization of hematopoietic progenitor cells using flow cytometry. Finally, osteoclast yield and functionality based on resorptive activity, Cathepsin K and tartrate-resistant acid phosphatase (TRAP) expression were assessed. The results were validated using qRT-PCR throughout the differentiation stages. RESULTS: Embryoid body-based differentiation yielded CD45(+), CD14(+), CD11b(+) subpopulations which in turn differentiated into osteoclasts which demonstrated TRAP positivity, Cathepsin K expression and mineral resorptive capabilities. This was regardless of which iPSC line was used. Monolayer-based differentiation yielded lower quantities of hematopoietic cells that were mostly CD34(+) and did not subsequently differentiate into osteoclasts. CONCLUSIONS: The outcome of this study demonstrates the successful differentiation of osteoclasts from iPSCs in conjunction with the embryoid-based differentiation method, while the monolayer-based method did not yield osteoclasts. No differences were observed regarding osteoclast differentiation between the PBMC and fibroblast-derived iPSC lines. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03547-6. |
format | Online Article Text |
id | pubmed-10631132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106311322023-11-07 Comparison of osteoclast differentiation protocols from human induced pluripotent stem cells of different tissue origins Blümke, Alexander Ijeoma, Erica Simon, Jessica Wellington, Rachel Purwaningrum, Medania Doulatov, Sergei Leber, Elizabeth Scatena, Marta Giachelli, Cecilia M. Stem Cell Res Ther Research BACKGROUND: Ever since their discovery, induced pluripotent stem cells (iPSCs) have been extensively differentiated into a large variety of cell types. However, a limited amount of work has been dedicated to differentiating iPSCs into osteoclasts. While several differentiation protocols have been published, it remains unclear which protocols or differentiation methods are preferable regarding the differentiation of osteoclasts. METHODS: In this study, we compared the osteoclastogenesis capacity of a peripheral blood mononuclear cell (PBMC)-derived iPSC line to a fibroblast-derived iPSC line in conjunction with either embryoid body-based or monolayer-based differentiation strategies. Both cell lines and differentiation protocols were investigated regarding their ability to generate osteoclasts and their inherent robustness and ease of use. The ability of both cell lines to remain undifferentiated while propagating using a feeder-free system was assessed using alkaline phosphatase staining. This was followed by evaluating mesodermal differentiation and the characterization of hematopoietic progenitor cells using flow cytometry. Finally, osteoclast yield and functionality based on resorptive activity, Cathepsin K and tartrate-resistant acid phosphatase (TRAP) expression were assessed. The results were validated using qRT-PCR throughout the differentiation stages. RESULTS: Embryoid body-based differentiation yielded CD45(+), CD14(+), CD11b(+) subpopulations which in turn differentiated into osteoclasts which demonstrated TRAP positivity, Cathepsin K expression and mineral resorptive capabilities. This was regardless of which iPSC line was used. Monolayer-based differentiation yielded lower quantities of hematopoietic cells that were mostly CD34(+) and did not subsequently differentiate into osteoclasts. CONCLUSIONS: The outcome of this study demonstrates the successful differentiation of osteoclasts from iPSCs in conjunction with the embryoid-based differentiation method, while the monolayer-based method did not yield osteoclasts. No differences were observed regarding osteoclast differentiation between the PBMC and fibroblast-derived iPSC lines. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03547-6. BioMed Central 2023-11-07 /pmc/articles/PMC10631132/ /pubmed/37936199 http://dx.doi.org/10.1186/s13287-023-03547-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Blümke, Alexander Ijeoma, Erica Simon, Jessica Wellington, Rachel Purwaningrum, Medania Doulatov, Sergei Leber, Elizabeth Scatena, Marta Giachelli, Cecilia M. Comparison of osteoclast differentiation protocols from human induced pluripotent stem cells of different tissue origins |
title | Comparison of osteoclast differentiation protocols from human induced pluripotent stem cells of different tissue origins |
title_full | Comparison of osteoclast differentiation protocols from human induced pluripotent stem cells of different tissue origins |
title_fullStr | Comparison of osteoclast differentiation protocols from human induced pluripotent stem cells of different tissue origins |
title_full_unstemmed | Comparison of osteoclast differentiation protocols from human induced pluripotent stem cells of different tissue origins |
title_short | Comparison of osteoclast differentiation protocols from human induced pluripotent stem cells of different tissue origins |
title_sort | comparison of osteoclast differentiation protocols from human induced pluripotent stem cells of different tissue origins |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10631132/ https://www.ncbi.nlm.nih.gov/pubmed/37936199 http://dx.doi.org/10.1186/s13287-023-03547-6 |
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