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Osteoclastogenesis of human peripheral blood, bone marrow, and cord blood monocytes
Osteoclasts are multinucleated bone resorbing cells that can be differentiated from human monocytes in vitro. There are few studies comparing osteoclastogenesis of different monocyte sources. We compared monocytes from human bone marrow (BM), peripheral blood (PB), and umbilical cord blood (CB) and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992388/ https://www.ncbi.nlm.nih.gov/pubmed/36882450 http://dx.doi.org/10.1038/s41598-023-30701-0 |
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author | Vuoti, Ella Lehenkari, Petri Tuukkanen, Juha Glumoff, Virpi Kylmäoja, Elina |
author_facet | Vuoti, Ella Lehenkari, Petri Tuukkanen, Juha Glumoff, Virpi Kylmäoja, Elina |
author_sort | Vuoti, Ella |
collection | PubMed |
description | Osteoclasts are multinucleated bone resorbing cells that can be differentiated from human monocytes in vitro. There are few studies comparing osteoclastogenesis of different monocyte sources. We compared monocytes from human bone marrow (BM), peripheral blood (PB), and umbilical cord blood (CB) and their osteoclastogenic potential by culturing them with RANKL (20 and 80 ng/ml) and M-CSF (10 ng/ml) for 14 days. We also cultured cells without growth factors, as umbilical cord blood monocytes have been reported to be able to fuse spontaneously into osteoclasts. The data was analysed on d4, d8, d11, and d14. After culture with RANKL and M-CSF, all types of cell cultures developed TRACP -positive multinuclear cells that were able to form resorption pits on human bone slices. Only occasional multinuclear cells and small infrequent resorbed areas could be found in PB and CB-derived cultures without growth factors. BM-derived cells formed greater resorption areas than PB- and CB-derived monocytes. The greatest monocyte population in BM samples were intermediate (CD14(++)CD16(+)) and in PB and CB classical monocytes (76.3% and 54.4%, respectively). In conclusion, our data demonstrates that bone resorbing osteoclasts can be differentiated from BM, PB and CB. However, the osteoclast precursor origin can affect the osteoclast properties and function. |
format | Online Article Text |
id | pubmed-9992388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99923882023-03-09 Osteoclastogenesis of human peripheral blood, bone marrow, and cord blood monocytes Vuoti, Ella Lehenkari, Petri Tuukkanen, Juha Glumoff, Virpi Kylmäoja, Elina Sci Rep Article Osteoclasts are multinucleated bone resorbing cells that can be differentiated from human monocytes in vitro. There are few studies comparing osteoclastogenesis of different monocyte sources. We compared monocytes from human bone marrow (BM), peripheral blood (PB), and umbilical cord blood (CB) and their osteoclastogenic potential by culturing them with RANKL (20 and 80 ng/ml) and M-CSF (10 ng/ml) for 14 days. We also cultured cells without growth factors, as umbilical cord blood monocytes have been reported to be able to fuse spontaneously into osteoclasts. The data was analysed on d4, d8, d11, and d14. After culture with RANKL and M-CSF, all types of cell cultures developed TRACP -positive multinuclear cells that were able to form resorption pits on human bone slices. Only occasional multinuclear cells and small infrequent resorbed areas could be found in PB and CB-derived cultures without growth factors. BM-derived cells formed greater resorption areas than PB- and CB-derived monocytes. The greatest monocyte population in BM samples were intermediate (CD14(++)CD16(+)) and in PB and CB classical monocytes (76.3% and 54.4%, respectively). In conclusion, our data demonstrates that bone resorbing osteoclasts can be differentiated from BM, PB and CB. However, the osteoclast precursor origin can affect the osteoclast properties and function. Nature Publishing Group UK 2023-03-07 /pmc/articles/PMC9992388/ /pubmed/36882450 http://dx.doi.org/10.1038/s41598-023-30701-0 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/) . |
spellingShingle | Article Vuoti, Ella Lehenkari, Petri Tuukkanen, Juha Glumoff, Virpi Kylmäoja, Elina Osteoclastogenesis of human peripheral blood, bone marrow, and cord blood monocytes |
title | Osteoclastogenesis of human peripheral blood, bone marrow, and cord blood monocytes |
title_full | Osteoclastogenesis of human peripheral blood, bone marrow, and cord blood monocytes |
title_fullStr | Osteoclastogenesis of human peripheral blood, bone marrow, and cord blood monocytes |
title_full_unstemmed | Osteoclastogenesis of human peripheral blood, bone marrow, and cord blood monocytes |
title_short | Osteoclastogenesis of human peripheral blood, bone marrow, and cord blood monocytes |
title_sort | osteoclastogenesis of human peripheral blood, bone marrow, and cord blood monocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992388/ https://www.ncbi.nlm.nih.gov/pubmed/36882450 http://dx.doi.org/10.1038/s41598-023-30701-0 |
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