Cargando…

STAT3 activation by catalpol promotes osteogenesis-angiogenesis coupling, thus accelerating osteoporotic bone repair

BACKGROUND: Bone fracture repair has gained a lot of attention due to the high incidence of delayed union or even nonunion especially in osteoporotic patients, resulting in a dreadful impact on the quality of life. However, current therapies involve the costly expense and hence become unaffordable s...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Liang, Zhang, Ri-Yan, Xie, Jun, Yang, Jia-Yi, Fang, Kang-Hao, Hong, Chen-Xuan, Yang, Rong-Bo, Bsoul, Najeeb, Yang, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863540/
https://www.ncbi.nlm.nih.gov/pubmed/33541442
http://dx.doi.org/10.1186/s13287-021-02178-z
_version_ 1783647515752529920
author Chen, Liang
Zhang, Ri-Yan
Xie, Jun
Yang, Jia-Yi
Fang, Kang-Hao
Hong, Chen-Xuan
Yang, Rong-Bo
Bsoul, Najeeb
Yang, Lei
author_facet Chen, Liang
Zhang, Ri-Yan
Xie, Jun
Yang, Jia-Yi
Fang, Kang-Hao
Hong, Chen-Xuan
Yang, Rong-Bo
Bsoul, Najeeb
Yang, Lei
author_sort Chen, Liang
collection PubMed
description BACKGROUND: Bone fracture repair has gained a lot of attention due to the high incidence of delayed union or even nonunion especially in osteoporotic patients, resulting in a dreadful impact on the quality of life. However, current therapies involve the costly expense and hence become unaffordable strategies for fracture recovery. Herein, developing new strategies for better bone repair is essential and urgent. Catalpol treatment has been reported to attenuate bone loss and promote bone formation. However, the mechanisms underlying its effects remain unraveled. METHODS: Rat bone marrow mesenchymal stem cells (BMSCs) were isolated from rat femurs. BMSC osteogenic ability was assessed using ALP and ARS staining, immunofluorescence, and western blot analysis. BMSC-mediated angiogenic potentials were determined using the western blot analysis, ELISA testing, scratch wound assay, transwell migration assay, and tube formation assay. To investigate the molecular mechanism, the lentivirus transfection was used. Ovariectomized and sham-operated rats with calvaria defect were analyzed using micro-CT, H&E staining, Masson’s trichrome staining, microfil perfusion, sequential fluorescent labeling, and immunohistochemistry assessment after administrated with/without catalpol. RESULTS: Our results manifested that catalpol enhanced BMSC osteoblastic differentiation and promoted BMSC-mediated angiogenesis in vitro. More importantly, this was conducted via the JAK2/STAT3 pathway, as knockdown of STAT3 partially abolished beneficial effects in BMSCs. Besides, catalpol administration facilitated bone regeneration as well as vessel formation in an OVX-induced osteoporosis calvarial defect rat model. CONCLUSIONS: The data above showed that catalpol could promote osteogenic ability of BMSC and BMSC-dependent angiogenesis through activation of the JAK2/STAT3 axis, suggesting it may be an ideal therapeutic agent for clinical medication of osteoporotic bone fracture.
format Online
Article
Text
id pubmed-7863540
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-78635402021-02-08 STAT3 activation by catalpol promotes osteogenesis-angiogenesis coupling, thus accelerating osteoporotic bone repair Chen, Liang Zhang, Ri-Yan Xie, Jun Yang, Jia-Yi Fang, Kang-Hao Hong, Chen-Xuan Yang, Rong-Bo Bsoul, Najeeb Yang, Lei Stem Cell Res Ther Research BACKGROUND: Bone fracture repair has gained a lot of attention due to the high incidence of delayed union or even nonunion especially in osteoporotic patients, resulting in a dreadful impact on the quality of life. However, current therapies involve the costly expense and hence become unaffordable strategies for fracture recovery. Herein, developing new strategies for better bone repair is essential and urgent. Catalpol treatment has been reported to attenuate bone loss and promote bone formation. However, the mechanisms underlying its effects remain unraveled. METHODS: Rat bone marrow mesenchymal stem cells (BMSCs) were isolated from rat femurs. BMSC osteogenic ability was assessed using ALP and ARS staining, immunofluorescence, and western blot analysis. BMSC-mediated angiogenic potentials were determined using the western blot analysis, ELISA testing, scratch wound assay, transwell migration assay, and tube formation assay. To investigate the molecular mechanism, the lentivirus transfection was used. Ovariectomized and sham-operated rats with calvaria defect were analyzed using micro-CT, H&E staining, Masson’s trichrome staining, microfil perfusion, sequential fluorescent labeling, and immunohistochemistry assessment after administrated with/without catalpol. RESULTS: Our results manifested that catalpol enhanced BMSC osteoblastic differentiation and promoted BMSC-mediated angiogenesis in vitro. More importantly, this was conducted via the JAK2/STAT3 pathway, as knockdown of STAT3 partially abolished beneficial effects in BMSCs. Besides, catalpol administration facilitated bone regeneration as well as vessel formation in an OVX-induced osteoporosis calvarial defect rat model. CONCLUSIONS: The data above showed that catalpol could promote osteogenic ability of BMSC and BMSC-dependent angiogenesis through activation of the JAK2/STAT3 axis, suggesting it may be an ideal therapeutic agent for clinical medication of osteoporotic bone fracture. BioMed Central 2021-02-04 /pmc/articles/PMC7863540/ /pubmed/33541442 http://dx.doi.org/10.1186/s13287-021-02178-z Text en © The Author(s) 2021 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chen, Liang
Zhang, Ri-Yan
Xie, Jun
Yang, Jia-Yi
Fang, Kang-Hao
Hong, Chen-Xuan
Yang, Rong-Bo
Bsoul, Najeeb
Yang, Lei
STAT3 activation by catalpol promotes osteogenesis-angiogenesis coupling, thus accelerating osteoporotic bone repair
title STAT3 activation by catalpol promotes osteogenesis-angiogenesis coupling, thus accelerating osteoporotic bone repair
title_full STAT3 activation by catalpol promotes osteogenesis-angiogenesis coupling, thus accelerating osteoporotic bone repair
title_fullStr STAT3 activation by catalpol promotes osteogenesis-angiogenesis coupling, thus accelerating osteoporotic bone repair
title_full_unstemmed STAT3 activation by catalpol promotes osteogenesis-angiogenesis coupling, thus accelerating osteoporotic bone repair
title_short STAT3 activation by catalpol promotes osteogenesis-angiogenesis coupling, thus accelerating osteoporotic bone repair
title_sort stat3 activation by catalpol promotes osteogenesis-angiogenesis coupling, thus accelerating osteoporotic bone repair
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863540/
https://www.ncbi.nlm.nih.gov/pubmed/33541442
http://dx.doi.org/10.1186/s13287-021-02178-z
work_keys_str_mv AT chenliang stat3activationbycatalpolpromotesosteogenesisangiogenesiscouplingthusacceleratingosteoporoticbonerepair
AT zhangriyan stat3activationbycatalpolpromotesosteogenesisangiogenesiscouplingthusacceleratingosteoporoticbonerepair
AT xiejun stat3activationbycatalpolpromotesosteogenesisangiogenesiscouplingthusacceleratingosteoporoticbonerepair
AT yangjiayi stat3activationbycatalpolpromotesosteogenesisangiogenesiscouplingthusacceleratingosteoporoticbonerepair
AT fangkanghao stat3activationbycatalpolpromotesosteogenesisangiogenesiscouplingthusacceleratingosteoporoticbonerepair
AT hongchenxuan stat3activationbycatalpolpromotesosteogenesisangiogenesiscouplingthusacceleratingosteoporoticbonerepair
AT yangrongbo stat3activationbycatalpolpromotesosteogenesisangiogenesiscouplingthusacceleratingosteoporoticbonerepair
AT bsoulnajeeb stat3activationbycatalpolpromotesosteogenesisangiogenesiscouplingthusacceleratingosteoporoticbonerepair
AT yanglei stat3activationbycatalpolpromotesosteogenesisangiogenesiscouplingthusacceleratingosteoporoticbonerepair