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Bone Injury and Repair Trigger Central and Peripheral NPY Neuronal Pathways

Bibliographic Details
Main Author: Alves,CJ
Publication Date: 2016
Other Authors: Alencastre,IS, Neto,E, Ribas,J, Ferreira,S, Daniel Marques Vasconcelos, Sousa,DM, Summavielle,T, Lamghari,M
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://repositorio.inesctec.pt/handle/123456789/6990
http://dx.doi.org/10.1371/journal.pone.0165465
Summary: Bone repair is a specialized type of wound repair controlled by complex multi-factorial events. The nervous system is recognized as one of the key regulators of bone mass, thereby suggesting a role for neuronal pathways in bone homeostasis. However, in the context of bone injury and repair, little is known on the interplay between the nervous system and bone. Here, we addressed the neuropeptide Y (NPY) neuronal arm during the initial stages of bone repair encompassing the inflammatory response and ossification phases in femoral-defect mouse model. Spatial and temporal analysis of transcriptional and protein levels of NPY and its receptors, Y1R and Y2R, reported to be involved in bone homeostasis, was performed in bone, dorsal root ganglia (DRG) and hypothalamus after femoral injury. The results showed that NPY system activity is increased in a time- and space-dependent manner during bone repair. Y1R expression was trigged in both bone and DRG throughout the inflammatory phase, while a Y2R response was restricted to the hypothalamus and at a later stage, during the ossification step. Our results provide new insights into the involvement of NPY neuronal pathways in bone repair.
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spelling Bone Injury and Repair Trigger Central and Peripheral NPY Neuronal PathwaysBone repair is a specialized type of wound repair controlled by complex multi-factorial events. The nervous system is recognized as one of the key regulators of bone mass, thereby suggesting a role for neuronal pathways in bone homeostasis. However, in the context of bone injury and repair, little is known on the interplay between the nervous system and bone. Here, we addressed the neuropeptide Y (NPY) neuronal arm during the initial stages of bone repair encompassing the inflammatory response and ossification phases in femoral-defect mouse model. Spatial and temporal analysis of transcriptional and protein levels of NPY and its receptors, Y1R and Y2R, reported to be involved in bone homeostasis, was performed in bone, dorsal root ganglia (DRG) and hypothalamus after femoral injury. The results showed that NPY system activity is increased in a time- and space-dependent manner during bone repair. Y1R expression was trigged in both bone and DRG throughout the inflammatory phase, while a Y2R response was restricted to the hypothalamus and at a later stage, during the ossification step. Our results provide new insights into the involvement of NPY neuronal pathways in bone repair.2018-01-18T16:27:25Z2016-01-01T00:00:00Z2016info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://repositorio.inesctec.pt/handle/123456789/6990http://dx.doi.org/10.1371/journal.pone.0165465engAlves,CJAlencastre,ISNeto,ERibas,JFerreira,SDaniel Marques VasconcelosSousa,DMSummavielle,TLamghari,Minfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-10-12T02:21:27Zoai:repositorio.inesctec.pt:123456789/6990Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T18:57:43.142652Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Bone Injury and Repair Trigger Central and Peripheral NPY Neuronal Pathways
title Bone Injury and Repair Trigger Central and Peripheral NPY Neuronal Pathways
spellingShingle Bone Injury and Repair Trigger Central and Peripheral NPY Neuronal Pathways
Alves,CJ
title_short Bone Injury and Repair Trigger Central and Peripheral NPY Neuronal Pathways
title_full Bone Injury and Repair Trigger Central and Peripheral NPY Neuronal Pathways
title_fullStr Bone Injury and Repair Trigger Central and Peripheral NPY Neuronal Pathways
title_full_unstemmed Bone Injury and Repair Trigger Central and Peripheral NPY Neuronal Pathways
title_sort Bone Injury and Repair Trigger Central and Peripheral NPY Neuronal Pathways
author Alves,CJ
author_facet Alves,CJ
Alencastre,IS
Neto,E
Ribas,J
Ferreira,S
Daniel Marques Vasconcelos
Sousa,DM
Summavielle,T
Lamghari,M
author_role author
author2 Alencastre,IS
Neto,E
Ribas,J
Ferreira,S
Daniel Marques Vasconcelos
Sousa,DM
Summavielle,T
Lamghari,M
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Alves,CJ
Alencastre,IS
Neto,E
Ribas,J
Ferreira,S
Daniel Marques Vasconcelos
Sousa,DM
Summavielle,T
Lamghari,M
description Bone repair is a specialized type of wound repair controlled by complex multi-factorial events. The nervous system is recognized as one of the key regulators of bone mass, thereby suggesting a role for neuronal pathways in bone homeostasis. However, in the context of bone injury and repair, little is known on the interplay between the nervous system and bone. Here, we addressed the neuropeptide Y (NPY) neuronal arm during the initial stages of bone repair encompassing the inflammatory response and ossification phases in femoral-defect mouse model. Spatial and temporal analysis of transcriptional and protein levels of NPY and its receptors, Y1R and Y2R, reported to be involved in bone homeostasis, was performed in bone, dorsal root ganglia (DRG) and hypothalamus after femoral injury. The results showed that NPY system activity is increased in a time- and space-dependent manner during bone repair. Y1R expression was trigged in both bone and DRG throughout the inflammatory phase, while a Y2R response was restricted to the hypothalamus and at a later stage, during the ossification step. Our results provide new insights into the involvement of NPY neuronal pathways in bone repair.
publishDate 2016
dc.date.none.fl_str_mv 2016-01-01T00:00:00Z
2016
2018-01-18T16:27:25Z
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http://dx.doi.org/10.1371/journal.pone.0165465
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