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Cell cytoskeleton and proliferation study for the RANKL‐induced RAW264.7 differentiation
Although document studies (including ours) have been reported the achieved in vitro osteoclastic cellular model establishment from the RAW264.7 cell lineage, there was no study directly reported that American Type Culture Collection (ATCC) cell bank has various RAW264.7 cell lineages. Besides that,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107080/ https://www.ncbi.nlm.nih.gov/pubmed/33742541 http://dx.doi.org/10.1111/jcmm.16390 |
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author | Kong, Lingbo Ma, Rui Cao, Yang Smith, Wanli Liu, Yuan Yang, Xiaobin Yan, Liang |
author_facet | Kong, Lingbo Ma, Rui Cao, Yang Smith, Wanli Liu, Yuan Yang, Xiaobin Yan, Liang |
author_sort | Kong, Lingbo |
collection | PubMed |
description | Although document studies (including ours) have been reported the achieved in vitro osteoclastic cellular model establishment from the RAW264.7 cell lineage, there was no study directly reported that American Type Culture Collection (ATCC) cell bank has various RAW264.7 cell lineages. Besides that, for our knowledge there was only one study compared the two different RAW264.7(TIB‐71) and RAW264.7(CRL‐2278) cell lineages for their osteoclastic differentiation, and they concluded that the RAW264.7(CRL‐2278) demonstrated to generate much osteoclast than RAW264.7(TIB‐71). However, on the contrary to their results we noticed the fusion of RAW264.7(TIB‐71) in our previous studies was much compromising. Therefore, we try to explore the two cell lineages for their properties in osteoclastic differentiation with an in‐depth cellular cytoskeletal study. Our current study has showed that comparing to the RAW264.7(CRL‐2278), RAW264.7(TIB‐71) demonstrated a much higher efficacies for RANKL‐stimulated osteoclastic differentiation. Besides that, in our depth cytoskeletal studies, we found that the RANKL‐induced RAW264.7(TIB‐71) cells could finally differentiate into mature osteoclasts. However, regardless the various pre‐treatment conditions, there was no mature osteoclast formed in RANKL‐induced RAW264.7(CRL‐2278) cell lineage. |
format | Online Article Text |
id | pubmed-8107080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81070802021-05-10 Cell cytoskeleton and proliferation study for the RANKL‐induced RAW264.7 differentiation Kong, Lingbo Ma, Rui Cao, Yang Smith, Wanli Liu, Yuan Yang, Xiaobin Yan, Liang J Cell Mol Med Original Articles Although document studies (including ours) have been reported the achieved in vitro osteoclastic cellular model establishment from the RAW264.7 cell lineage, there was no study directly reported that American Type Culture Collection (ATCC) cell bank has various RAW264.7 cell lineages. Besides that, for our knowledge there was only one study compared the two different RAW264.7(TIB‐71) and RAW264.7(CRL‐2278) cell lineages for their osteoclastic differentiation, and they concluded that the RAW264.7(CRL‐2278) demonstrated to generate much osteoclast than RAW264.7(TIB‐71). However, on the contrary to their results we noticed the fusion of RAW264.7(TIB‐71) in our previous studies was much compromising. Therefore, we try to explore the two cell lineages for their properties in osteoclastic differentiation with an in‐depth cellular cytoskeletal study. Our current study has showed that comparing to the RAW264.7(CRL‐2278), RAW264.7(TIB‐71) demonstrated a much higher efficacies for RANKL‐stimulated osteoclastic differentiation. Besides that, in our depth cytoskeletal studies, we found that the RANKL‐induced RAW264.7(TIB‐71) cells could finally differentiate into mature osteoclasts. However, regardless the various pre‐treatment conditions, there was no mature osteoclast formed in RANKL‐induced RAW264.7(CRL‐2278) cell lineage. John Wiley and Sons Inc. 2021-03-19 2021-05 /pmc/articles/PMC8107080/ /pubmed/33742541 http://dx.doi.org/10.1111/jcmm.16390 Text en © 2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Kong, Lingbo Ma, Rui Cao, Yang Smith, Wanli Liu, Yuan Yang, Xiaobin Yan, Liang Cell cytoskeleton and proliferation study for the RANKL‐induced RAW264.7 differentiation |
title | Cell cytoskeleton and proliferation study for the RANKL‐induced RAW264.7 differentiation |
title_full | Cell cytoskeleton and proliferation study for the RANKL‐induced RAW264.7 differentiation |
title_fullStr | Cell cytoskeleton and proliferation study for the RANKL‐induced RAW264.7 differentiation |
title_full_unstemmed | Cell cytoskeleton and proliferation study for the RANKL‐induced RAW264.7 differentiation |
title_short | Cell cytoskeleton and proliferation study for the RANKL‐induced RAW264.7 differentiation |
title_sort | cell cytoskeleton and proliferation study for the rankl‐induced raw264.7 differentiation |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107080/ https://www.ncbi.nlm.nih.gov/pubmed/33742541 http://dx.doi.org/10.1111/jcmm.16390 |
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