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The Indispensable Role of Cyclin-Dependent Kinase 1 in Skeletal Development
Skeletal development is tightly regulated through the processes of chondrocyte proliferation and differentiation. Although the involvement of transcription and growth factors on the regulation of skeletal development has been extensively studied, the role of cell cycle regulatory proteins in this pr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816159/ https://www.ncbi.nlm.nih.gov/pubmed/26860366 http://dx.doi.org/10.1038/srep20622 |
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author | Saito, Masanori Mulati, Mieradili Talib, S. Zakiah A. Kaldis, Philipp Takeda, Shu Okawa, Atsushi Inose, Hiroyuki |
author_facet | Saito, Masanori Mulati, Mieradili Talib, S. Zakiah A. Kaldis, Philipp Takeda, Shu Okawa, Atsushi Inose, Hiroyuki |
author_sort | Saito, Masanori |
collection | PubMed |
description | Skeletal development is tightly regulated through the processes of chondrocyte proliferation and differentiation. Although the involvement of transcription and growth factors on the regulation of skeletal development has been extensively studied, the role of cell cycle regulatory proteins in this process remains elusive. To date, through cell-specific loss-of-function experiments in vivo, no cell cycle regulatory proteins have yet been conclusively shown to regulate skeletal development. Here, we demonstrate that cyclin-dependent kinase 1 (Cdk1) regulates skeletal development based on chondrocyte-specific loss-of-function experiments performed in a mouse model. Cdk1 is highly expressed in columnar proliferative chondrocytes and is greatly downregulated upon differentiation into hypertrophic chondrocytes. Cdk1 is essential for proper chondrocyte proliferation and deletion of Cdk1 resulted in accelerated differentiation of chondrocytes. In vitro and ex vivo analyses revealed that Cdk1 is an essential cell cycle regulatory protein for parathyroid hormone-related peptide (PTHrP) signaling pathway, which is critical to chondrocyte proliferation and differentiation. These results demonstrate that Cdk1 functions as a molecular switch from proliferation to hypertrophic differentiation of chondrocytes and thus is indispensable for skeletal development. Given the availability of inhibitors of Cdk1 activity, our results could provide insight for the treatment of diseases involving abnormal chondrocyte proliferation, such as osteoarthritis. |
format | Online Article Text |
id | pubmed-4816159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48161592016-04-05 The Indispensable Role of Cyclin-Dependent Kinase 1 in Skeletal Development Saito, Masanori Mulati, Mieradili Talib, S. Zakiah A. Kaldis, Philipp Takeda, Shu Okawa, Atsushi Inose, Hiroyuki Sci Rep Article Skeletal development is tightly regulated through the processes of chondrocyte proliferation and differentiation. Although the involvement of transcription and growth factors on the regulation of skeletal development has been extensively studied, the role of cell cycle regulatory proteins in this process remains elusive. To date, through cell-specific loss-of-function experiments in vivo, no cell cycle regulatory proteins have yet been conclusively shown to regulate skeletal development. Here, we demonstrate that cyclin-dependent kinase 1 (Cdk1) regulates skeletal development based on chondrocyte-specific loss-of-function experiments performed in a mouse model. Cdk1 is highly expressed in columnar proliferative chondrocytes and is greatly downregulated upon differentiation into hypertrophic chondrocytes. Cdk1 is essential for proper chondrocyte proliferation and deletion of Cdk1 resulted in accelerated differentiation of chondrocytes. In vitro and ex vivo analyses revealed that Cdk1 is an essential cell cycle regulatory protein for parathyroid hormone-related peptide (PTHrP) signaling pathway, which is critical to chondrocyte proliferation and differentiation. These results demonstrate that Cdk1 functions as a molecular switch from proliferation to hypertrophic differentiation of chondrocytes and thus is indispensable for skeletal development. Given the availability of inhibitors of Cdk1 activity, our results could provide insight for the treatment of diseases involving abnormal chondrocyte proliferation, such as osteoarthritis. Nature Publishing Group 2016-02-10 /pmc/articles/PMC4816159/ /pubmed/26860366 http://dx.doi.org/10.1038/srep20622 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Saito, Masanori Mulati, Mieradili Talib, S. Zakiah A. Kaldis, Philipp Takeda, Shu Okawa, Atsushi Inose, Hiroyuki The Indispensable Role of Cyclin-Dependent Kinase 1 in Skeletal Development |
title | The Indispensable Role of Cyclin-Dependent Kinase 1 in Skeletal Development |
title_full | The Indispensable Role of Cyclin-Dependent Kinase 1 in Skeletal Development |
title_fullStr | The Indispensable Role of Cyclin-Dependent Kinase 1 in Skeletal Development |
title_full_unstemmed | The Indispensable Role of Cyclin-Dependent Kinase 1 in Skeletal Development |
title_short | The Indispensable Role of Cyclin-Dependent Kinase 1 in Skeletal Development |
title_sort | indispensable role of cyclin-dependent kinase 1 in skeletal development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816159/ https://www.ncbi.nlm.nih.gov/pubmed/26860366 http://dx.doi.org/10.1038/srep20622 |
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