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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...

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Autores principales: Wang, Shaoyi, Li, Mengyu, Zhang, Wenjie, Hua, Hongfei, Wang, Ningtao, Zhao, Jun, Ge, Jing, Jiang, Xinquan, Zhang, Zhiyuan, Ye, Dongxia, Yang, Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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.
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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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