Cargando…

Adenovirus-mediated delivery of Sema3A alleviates rheumatoid arthritis in a serum-transfer induced mouse model

Rheumatoid arthritis is a chronic autoimmune disease characterized by infiltration of inflammatory cells into the synovium and destruction of cartilage and bone. Macrophages, fibroblast-like synoviocytes (FLS), and osteoclasts are critical cells driving the pathogenesis of RA. Semaphorin 3A (Sema3A)...

Descripción completa

Detalles Bibliográficos
Autores principales: Teng, Yue, Yin, Zhanhai, Li, Jing, Li, Kun, Li, Xu, Zhang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630410/
https://www.ncbi.nlm.nih.gov/pubmed/29029510
http://dx.doi.org/10.18632/oncotarget.19915
_version_ 1783269220581113856
author Teng, Yue
Yin, Zhanhai
Li, Jing
Li, Kun
Li, Xu
Zhang, Yan
author_facet Teng, Yue
Yin, Zhanhai
Li, Jing
Li, Kun
Li, Xu
Zhang, Yan
author_sort Teng, Yue
collection PubMed
description Rheumatoid arthritis is a chronic autoimmune disease characterized by infiltration of inflammatory cells into the synovium and destruction of cartilage and bone. Macrophages, fibroblast-like synoviocytes (FLS), and osteoclasts are critical cells driving the pathogenesis of RA. Semaphorin 3A (Sema3A) is recently identified as an essential player in the bone homeostasis, however its role in RA progression especially in the macrophage polarization are poorly understood. In the present study, we found that Sems3A levels were significantly decreased in RA serum and synovial fluid compared to OA controls. There was a negative correlation between Sema3A levels and RA severity. Using in vitro cell cultures, we showed for the first time that Sema3A promoted IL-4 induced M2 macrophage polarization, whereas prohibited LPS/IFN-γ induced M1 polarization. Sema3A inhibited VEGF-induced endothelial cells proliferation and migration, suppressed VEGF-mediated invasion and IL-6 production of FLS while stimulating their apoptosis. In addition, Sema3A retarded osteoclastogenesis. In vivo data demonstrated that Sema3A administration attenuated joint tissue damage and the severity of experimental arthritis. Our findings uncovered Sema3A as a promising diagnostic biomarker and novel prevention and treatment strategies in arthritis treatment.
format Online
Article
Text
id pubmed-5630410
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-56304102017-10-12 Adenovirus-mediated delivery of Sema3A alleviates rheumatoid arthritis in a serum-transfer induced mouse model Teng, Yue Yin, Zhanhai Li, Jing Li, Kun Li, Xu Zhang, Yan Oncotarget Research Paper Rheumatoid arthritis is a chronic autoimmune disease characterized by infiltration of inflammatory cells into the synovium and destruction of cartilage and bone. Macrophages, fibroblast-like synoviocytes (FLS), and osteoclasts are critical cells driving the pathogenesis of RA. Semaphorin 3A (Sema3A) is recently identified as an essential player in the bone homeostasis, however its role in RA progression especially in the macrophage polarization are poorly understood. In the present study, we found that Sems3A levels were significantly decreased in RA serum and synovial fluid compared to OA controls. There was a negative correlation between Sema3A levels and RA severity. Using in vitro cell cultures, we showed for the first time that Sema3A promoted IL-4 induced M2 macrophage polarization, whereas prohibited LPS/IFN-γ induced M1 polarization. Sema3A inhibited VEGF-induced endothelial cells proliferation and migration, suppressed VEGF-mediated invasion and IL-6 production of FLS while stimulating their apoptosis. In addition, Sema3A retarded osteoclastogenesis. In vivo data demonstrated that Sema3A administration attenuated joint tissue damage and the severity of experimental arthritis. Our findings uncovered Sema3A as a promising diagnostic biomarker and novel prevention and treatment strategies in arthritis treatment. Impact Journals LLC 2017-08-03 /pmc/articles/PMC5630410/ /pubmed/29029510 http://dx.doi.org/10.18632/oncotarget.19915 Text en Copyright: © 2017 Teng et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Teng, Yue
Yin, Zhanhai
Li, Jing
Li, Kun
Li, Xu
Zhang, Yan
Adenovirus-mediated delivery of Sema3A alleviates rheumatoid arthritis in a serum-transfer induced mouse model
title Adenovirus-mediated delivery of Sema3A alleviates rheumatoid arthritis in a serum-transfer induced mouse model
title_full Adenovirus-mediated delivery of Sema3A alleviates rheumatoid arthritis in a serum-transfer induced mouse model
title_fullStr Adenovirus-mediated delivery of Sema3A alleviates rheumatoid arthritis in a serum-transfer induced mouse model
title_full_unstemmed Adenovirus-mediated delivery of Sema3A alleviates rheumatoid arthritis in a serum-transfer induced mouse model
title_short Adenovirus-mediated delivery of Sema3A alleviates rheumatoid arthritis in a serum-transfer induced mouse model
title_sort adenovirus-mediated delivery of sema3a alleviates rheumatoid arthritis in a serum-transfer induced mouse model
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630410/
https://www.ncbi.nlm.nih.gov/pubmed/29029510
http://dx.doi.org/10.18632/oncotarget.19915
work_keys_str_mv AT tengyue adenovirusmediateddeliveryofsema3aalleviatesrheumatoidarthritisinaserumtransferinducedmousemodel
AT yinzhanhai adenovirusmediateddeliveryofsema3aalleviatesrheumatoidarthritisinaserumtransferinducedmousemodel
AT lijing adenovirusmediateddeliveryofsema3aalleviatesrheumatoidarthritisinaserumtransferinducedmousemodel
AT likun adenovirusmediateddeliveryofsema3aalleviatesrheumatoidarthritisinaserumtransferinducedmousemodel
AT lixu adenovirusmediateddeliveryofsema3aalleviatesrheumatoidarthritisinaserumtransferinducedmousemodel
AT zhangyan adenovirusmediateddeliveryofsema3aalleviatesrheumatoidarthritisinaserumtransferinducedmousemodel