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Cell-free fat extract attenuates osteoarthritis via chondrocytes regeneration and macrophages immunomodulation

BACKGROUND: The prevalence of osteoarthritis (OA) is increasing, yet clinically effective and economical treatments are unavailable. We have previously proposed a cell-free fat extract (CEFFE) containing multiple cytokines, which possessed antiapoptotic, anti-oxidative, and proliferation promotion f...

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Autores principales: Jia, Zhuoxuan, Kang, Bijun, Cai, Yizuo, Chen, Chingyu, Yu, Zheyuan, Li, Wei, Zhang, Wenjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973552/
https://www.ncbi.nlm.nih.gov/pubmed/35365233
http://dx.doi.org/10.1186/s13287-022-02813-3
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author Jia, Zhuoxuan
Kang, Bijun
Cai, Yizuo
Chen, Chingyu
Yu, Zheyuan
Li, Wei
Zhang, Wenjie
author_facet Jia, Zhuoxuan
Kang, Bijun
Cai, Yizuo
Chen, Chingyu
Yu, Zheyuan
Li, Wei
Zhang, Wenjie
author_sort Jia, Zhuoxuan
collection PubMed
description BACKGROUND: The prevalence of osteoarthritis (OA) is increasing, yet clinically effective and economical treatments are unavailable. We have previously proposed a cell-free fat extract (CEFFE) containing multiple cytokines, which possessed antiapoptotic, anti-oxidative, and proliferation promotion functions, as a “cell-free” strategy. In this study, we aimed to evaluate the therapeutic effect of CEFFE in vivo and in vitro. METHODS: In vivo study, sodium iodoacetate-induced OA rats were treated with CEFFE by intra-articular injections for 8 weeks. Behavioral experiments were performed every two weeks. Histological analyses, anti-type II collagen, and toluidine staining provided structural evaluation. Macrophage infiltration was assessed by anti-CD68 and anti-CD206 staining. In vitro study, the effect of CEFFE on macrophage polarization and secretory factors was evaluated by flow cytometry, immunofluorescence, and quantitative reverse-transcription polymerase chain reaction (qRT-PCR). The effect of CEFFE on cartilage regeneration was accessed by cell counting kit-8 assay and qRT-PCR. The generation of reactive oxygen species (ROS) and levels of ROS-related enzymes were investigated by qRT-PCR and western blotting. RESULTS: In rat models with sodium iodoacetate (MIA)-induced OA, CEFFE increased claw retraction pressure while decreasing bipedal pressure in a dose-dependent manner. Moreover, CEFFE promoted cartilage structure restoration and increased the proportion of CD206(+) macrophages in the synovium. In vitro, CEFFE decreased the proportion of CD86(+) cells and reduced the expression of pro-inflammatory factors in LPS + IFN-γ induced Raw 264.7. In addition, CEFFE decreased the expression of interleukin-6 and ADAMTs-5 and promoted the expression of SOX-9 in mouse primary chondrocytes. Besides, CEFFE reduced the intracellular levels of reactive oxygen species in both in vitro models through regulating ROS-related enzymes. CONCLUSIONS: CEFFE inhibits the progression of OA by promoting cartilage regeneration and limiting low-grade joint inflammation. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-02813-3.
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spelling pubmed-89735522022-04-02 Cell-free fat extract attenuates osteoarthritis via chondrocytes regeneration and macrophages immunomodulation Jia, Zhuoxuan Kang, Bijun Cai, Yizuo Chen, Chingyu Yu, Zheyuan Li, Wei Zhang, Wenjie Stem Cell Res Ther Research BACKGROUND: The prevalence of osteoarthritis (OA) is increasing, yet clinically effective and economical treatments are unavailable. We have previously proposed a cell-free fat extract (CEFFE) containing multiple cytokines, which possessed antiapoptotic, anti-oxidative, and proliferation promotion functions, as a “cell-free” strategy. In this study, we aimed to evaluate the therapeutic effect of CEFFE in vivo and in vitro. METHODS: In vivo study, sodium iodoacetate-induced OA rats were treated with CEFFE by intra-articular injections for 8 weeks. Behavioral experiments were performed every two weeks. Histological analyses, anti-type II collagen, and toluidine staining provided structural evaluation. Macrophage infiltration was assessed by anti-CD68 and anti-CD206 staining. In vitro study, the effect of CEFFE on macrophage polarization and secretory factors was evaluated by flow cytometry, immunofluorescence, and quantitative reverse-transcription polymerase chain reaction (qRT-PCR). The effect of CEFFE on cartilage regeneration was accessed by cell counting kit-8 assay and qRT-PCR. The generation of reactive oxygen species (ROS) and levels of ROS-related enzymes were investigated by qRT-PCR and western blotting. RESULTS: In rat models with sodium iodoacetate (MIA)-induced OA, CEFFE increased claw retraction pressure while decreasing bipedal pressure in a dose-dependent manner. Moreover, CEFFE promoted cartilage structure restoration and increased the proportion of CD206(+) macrophages in the synovium. In vitro, CEFFE decreased the proportion of CD86(+) cells and reduced the expression of pro-inflammatory factors in LPS + IFN-γ induced Raw 264.7. In addition, CEFFE decreased the expression of interleukin-6 and ADAMTs-5 and promoted the expression of SOX-9 in mouse primary chondrocytes. Besides, CEFFE reduced the intracellular levels of reactive oxygen species in both in vitro models through regulating ROS-related enzymes. CONCLUSIONS: CEFFE inhibits the progression of OA by promoting cartilage regeneration and limiting low-grade joint inflammation. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-02813-3. BioMed Central 2022-04-01 /pmc/articles/PMC8973552/ /pubmed/35365233 http://dx.doi.org/10.1186/s13287-022-02813-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Jia, Zhuoxuan
Kang, Bijun
Cai, Yizuo
Chen, Chingyu
Yu, Zheyuan
Li, Wei
Zhang, Wenjie
Cell-free fat extract attenuates osteoarthritis via chondrocytes regeneration and macrophages immunomodulation
title Cell-free fat extract attenuates osteoarthritis via chondrocytes regeneration and macrophages immunomodulation
title_full Cell-free fat extract attenuates osteoarthritis via chondrocytes regeneration and macrophages immunomodulation
title_fullStr Cell-free fat extract attenuates osteoarthritis via chondrocytes regeneration and macrophages immunomodulation
title_full_unstemmed Cell-free fat extract attenuates osteoarthritis via chondrocytes regeneration and macrophages immunomodulation
title_short Cell-free fat extract attenuates osteoarthritis via chondrocytes regeneration and macrophages immunomodulation
title_sort cell-free fat extract attenuates osteoarthritis via chondrocytes regeneration and macrophages immunomodulation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973552/
https://www.ncbi.nlm.nih.gov/pubmed/35365233
http://dx.doi.org/10.1186/s13287-022-02813-3
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