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Growth differentiation factor 15 promotes blood vessel growth by stimulating cell cycle progression in repair of critical-sized calvarial defect
Repair of large bone defects remains a challenge for surgeons, tissue engineering represents a promising approach. However, the use of this technique is limited by delayed vascularization in central regions of the scaffold. Growth differentiation factor 15(GDF15) has recently been reported to be a p...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567281/ https://www.ncbi.nlm.nih.gov/pubmed/28831101 http://dx.doi.org/10.1038/s41598-017-09210-4 |
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author | Wang, Shaoyi Li, Mengyu Zhang, Wenjie Hua, Hongfei Wang, Ningtao Zhao, Jun Ge, Jing Jiang, Xinquan Zhang, Zhiyuan Ye, Dongxia Yang, Chi |
author_facet | Wang, Shaoyi Li, Mengyu Zhang, Wenjie Hua, Hongfei Wang, Ningtao Zhao, Jun Ge, Jing Jiang, Xinquan Zhang, Zhiyuan Ye, Dongxia Yang, Chi |
author_sort | Wang, Shaoyi |
collection | PubMed |
description | Repair of large bone defects remains a challenge for surgeons, tissue engineering represents a promising approach. However, the use of this technique is limited by delayed vascularization in central regions of the scaffold. Growth differentiation factor 15(GDF15) has recently been reported to be a potential angiogenic cytokine and has an ability to promote the proliferation of human umbilical vein endothelial cells(HUVECs). Whether it can be applied for promoting vascularized bone regeneration is still unknown. In this study, we demonstrated that GDF15 augmented the expression of cyclins D1 and E, induced Rb phosphorylation and E2F-1 nuclear translocation, as well as increased HUVECs proliferation. Furthermore, we also observed that GDF15 promoted the formation of functional vessels at an artificially-induced angiogenic site, and remarkably improved the healing in the repair of critical-sized calvarial defects. Our results confirm the essential role of GDF15 in angiogenesis and suggest its potential beneficial use in regenerative medicine. |
format | Online Article Text |
id | pubmed-5567281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55672812017-09-01 Growth differentiation factor 15 promotes blood vessel growth by stimulating cell cycle progression in repair of critical-sized calvarial defect Wang, Shaoyi Li, Mengyu Zhang, Wenjie Hua, Hongfei Wang, Ningtao Zhao, Jun Ge, Jing Jiang, Xinquan Zhang, Zhiyuan Ye, Dongxia Yang, Chi Sci Rep Article Repair of large bone defects remains a challenge for surgeons, tissue engineering represents a promising approach. However, the use of this technique is limited by delayed vascularization in central regions of the scaffold. Growth differentiation factor 15(GDF15) has recently been reported to be a potential angiogenic cytokine and has an ability to promote the proliferation of human umbilical vein endothelial cells(HUVECs). Whether it can be applied for promoting vascularized bone regeneration is still unknown. In this study, we demonstrated that GDF15 augmented the expression of cyclins D1 and E, induced Rb phosphorylation and E2F-1 nuclear translocation, as well as increased HUVECs proliferation. Furthermore, we also observed that GDF15 promoted the formation of functional vessels at an artificially-induced angiogenic site, and remarkably improved the healing in the repair of critical-sized calvarial defects. Our results confirm the essential role of GDF15 in angiogenesis and suggest its potential beneficial use in regenerative medicine. Nature Publishing Group UK 2017-08-22 /pmc/articles/PMC5567281/ /pubmed/28831101 http://dx.doi.org/10.1038/s41598-017-09210-4 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Shaoyi Li, Mengyu Zhang, Wenjie Hua, Hongfei Wang, Ningtao Zhao, Jun Ge, Jing Jiang, Xinquan Zhang, Zhiyuan Ye, Dongxia Yang, Chi Growth differentiation factor 15 promotes blood vessel growth by stimulating cell cycle progression in repair of critical-sized calvarial defect |
title | Growth differentiation factor 15 promotes blood vessel growth by stimulating cell cycle progression in repair of critical-sized calvarial defect |
title_full | Growth differentiation factor 15 promotes blood vessel growth by stimulating cell cycle progression in repair of critical-sized calvarial defect |
title_fullStr | Growth differentiation factor 15 promotes blood vessel growth by stimulating cell cycle progression in repair of critical-sized calvarial defect |
title_full_unstemmed | Growth differentiation factor 15 promotes blood vessel growth by stimulating cell cycle progression in repair of critical-sized calvarial defect |
title_short | Growth differentiation factor 15 promotes blood vessel growth by stimulating cell cycle progression in repair of critical-sized calvarial defect |
title_sort | growth differentiation factor 15 promotes blood vessel growth by stimulating cell cycle progression in repair of critical-sized calvarial defect |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567281/ https://www.ncbi.nlm.nih.gov/pubmed/28831101 http://dx.doi.org/10.1038/s41598-017-09210-4 |
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