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Feline umbilical cord-derived mesenchymal stem cells: isolation, identification, and antioxidative stress role through NF-κB signaling pathway

At present, the differentiation potential and antioxidant activity of feline umbilical cord-derived mesenchymal stem cells (UC-MSCs) have not been clearly studied. In this study, feline UC-MSCs were isolated by tissue adhesion method, identified by flow cytometry detection of cell surface markers (C...

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Autores principales: Zhai, Zhu-Hui, Li, Jun, You, Zhao, Cai, Yang, Yang, Jie, An, Jie, Zhao, Di-Peng, Wang, He-Jie, Dou, Min-Min, Du, Rong, Qin, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10249476/
https://www.ncbi.nlm.nih.gov/pubmed/37303730
http://dx.doi.org/10.3389/fvets.2023.1203012
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author Zhai, Zhu-Hui
Li, Jun
You, Zhao
Cai, Yang
Yang, Jie
An, Jie
Zhao, Di-Peng
Wang, He-Jie
Dou, Min-Min
Du, Rong
Qin, Jian
author_facet Zhai, Zhu-Hui
Li, Jun
You, Zhao
Cai, Yang
Yang, Jie
An, Jie
Zhao, Di-Peng
Wang, He-Jie
Dou, Min-Min
Du, Rong
Qin, Jian
author_sort Zhai, Zhu-Hui
collection PubMed
description At present, the differentiation potential and antioxidant activity of feline umbilical cord-derived mesenchymal stem cells (UC-MSCs) have not been clearly studied. In this study, feline UC-MSCs were isolated by tissue adhesion method, identified by flow cytometry detection of cell surface markers (CD44, CD90, CD34, and CD45), and induced differentiation toward osteogenesis and adipogenesis in vitro. Furthermore, the oxidative stress model was established with hydrogen peroxide (H(2)O(2)) (100 μM, 300 μM, 500 μM, 700 μM, and 900 μM). The antioxidant properties of feline UC-MSCs and feline fibroblasts were compared by morphological observation, ROS detection, cell viability via CCK-8 assay, as well as oxidative and antioxidative parameters via ELISA. The mRNA expression of genes related to NF-κB pathway was detected via quantitative real-time polymerase chain reaction, while the levels of NF-κB signaling cascade-related proteins were determined via Western Blot. The results showed that feline UC-MSCs highly expressed CD44 and CD90, while negative for CD34 and CD45 expression. Feline UC-MSCs cultured under osteogenic and adipogenic conditions showed good differentiation capacity. After being exposed to different concentrations of H(2)O(2) for eight hours, feline UC-MSCs exhibited the significantly higher survival rate than feline fibroblasts. A certain concentration of H(2)O(2) could up-regulate the activities of SOD2 and GSH-Px in feline UC-MSCs. The expression levels of p50, MnSOD, and FHC mRNA in feline UC-MSCs stimulated by 300 μM and 500 μM H(2)O(2) significantly increased compared with the control group. Furthermore, it was observed that 500 μM H(2)O(2) significantly enhanced the protein levels of p-IκB, IκB, p-p50, p50, MnSOD, and FHC, which could be reversed by BAY 11-7,082, a NF-κB signaling pathway inhibitor. In conclusion, it was confirmed that feline UC-MSCs, with good osteogenesis and adipogenesis abilities, had better antioxidant property which might be related to NF-κB signaling pathway. This study lays a foundation for the further application of feline UC-MSCs in treating the various inflammatory and oxidative injury diseases of pets.
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spelling pubmed-102494762023-06-09 Feline umbilical cord-derived mesenchymal stem cells: isolation, identification, and antioxidative stress role through NF-κB signaling pathway Zhai, Zhu-Hui Li, Jun You, Zhao Cai, Yang Yang, Jie An, Jie Zhao, Di-Peng Wang, He-Jie Dou, Min-Min Du, Rong Qin, Jian Front Vet Sci Veterinary Science At present, the differentiation potential and antioxidant activity of feline umbilical cord-derived mesenchymal stem cells (UC-MSCs) have not been clearly studied. In this study, feline UC-MSCs were isolated by tissue adhesion method, identified by flow cytometry detection of cell surface markers (CD44, CD90, CD34, and CD45), and induced differentiation toward osteogenesis and adipogenesis in vitro. Furthermore, the oxidative stress model was established with hydrogen peroxide (H(2)O(2)) (100 μM, 300 μM, 500 μM, 700 μM, and 900 μM). The antioxidant properties of feline UC-MSCs and feline fibroblasts were compared by morphological observation, ROS detection, cell viability via CCK-8 assay, as well as oxidative and antioxidative parameters via ELISA. The mRNA expression of genes related to NF-κB pathway was detected via quantitative real-time polymerase chain reaction, while the levels of NF-κB signaling cascade-related proteins were determined via Western Blot. The results showed that feline UC-MSCs highly expressed CD44 and CD90, while negative for CD34 and CD45 expression. Feline UC-MSCs cultured under osteogenic and adipogenic conditions showed good differentiation capacity. After being exposed to different concentrations of H(2)O(2) for eight hours, feline UC-MSCs exhibited the significantly higher survival rate than feline fibroblasts. A certain concentration of H(2)O(2) could up-regulate the activities of SOD2 and GSH-Px in feline UC-MSCs. The expression levels of p50, MnSOD, and FHC mRNA in feline UC-MSCs stimulated by 300 μM and 500 μM H(2)O(2) significantly increased compared with the control group. Furthermore, it was observed that 500 μM H(2)O(2) significantly enhanced the protein levels of p-IκB, IκB, p-p50, p50, MnSOD, and FHC, which could be reversed by BAY 11-7,082, a NF-κB signaling pathway inhibitor. In conclusion, it was confirmed that feline UC-MSCs, with good osteogenesis and adipogenesis abilities, had better antioxidant property which might be related to NF-κB signaling pathway. This study lays a foundation for the further application of feline UC-MSCs in treating the various inflammatory and oxidative injury diseases of pets. Frontiers Media S.A. 2023-05-25 /pmc/articles/PMC10249476/ /pubmed/37303730 http://dx.doi.org/10.3389/fvets.2023.1203012 Text en Copyright © 2023 Zhai, Li, You, Cai, Yang, An, Zhao, Wang, Dou, Du and Qin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Veterinary Science
Zhai, Zhu-Hui
Li, Jun
You, Zhao
Cai, Yang
Yang, Jie
An, Jie
Zhao, Di-Peng
Wang, He-Jie
Dou, Min-Min
Du, Rong
Qin, Jian
Feline umbilical cord-derived mesenchymal stem cells: isolation, identification, and antioxidative stress role through NF-κB signaling pathway
title Feline umbilical cord-derived mesenchymal stem cells: isolation, identification, and antioxidative stress role through NF-κB signaling pathway
title_full Feline umbilical cord-derived mesenchymal stem cells: isolation, identification, and antioxidative stress role through NF-κB signaling pathway
title_fullStr Feline umbilical cord-derived mesenchymal stem cells: isolation, identification, and antioxidative stress role through NF-κB signaling pathway
title_full_unstemmed Feline umbilical cord-derived mesenchymal stem cells: isolation, identification, and antioxidative stress role through NF-κB signaling pathway
title_short Feline umbilical cord-derived mesenchymal stem cells: isolation, identification, and antioxidative stress role through NF-κB signaling pathway
title_sort feline umbilical cord-derived mesenchymal stem cells: isolation, identification, and antioxidative stress role through nf-κb signaling pathway
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10249476/
https://www.ncbi.nlm.nih.gov/pubmed/37303730
http://dx.doi.org/10.3389/fvets.2023.1203012
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