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The involvement of transient receptor potential channels in mast cell activation by microbubbles

This study was to explore the activation of mast cells by microbubbles, with the focus on transient receptor potential (TRP) channels mediated degranulation and calcium influx. Bone marrow‐derived mast cells (BMMCs) were primarily obtained from femurs in mice and induced differentiation for 4 weeks....

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Autores principales: Liu, Jia, Qing, Long, He, Yufei, Zhu, Qihui, Xu, Weigang, Wu, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10660621/
https://www.ncbi.nlm.nih.gov/pubmed/37680043
http://dx.doi.org/10.1111/jcmm.17947
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author Liu, Jia
Qing, Long
He, Yufei
Zhu, Qihui
Xu, Weigang
Wu, Jianhua
author_facet Liu, Jia
Qing, Long
He, Yufei
Zhu, Qihui
Xu, Weigang
Wu, Jianhua
author_sort Liu, Jia
collection PubMed
description This study was to explore the activation of mast cells by microbubbles, with the focus on transient receptor potential (TRP) channels mediated degranulation and calcium influx. Bone marrow‐derived mast cells (BMMCs) were primarily obtained from femurs in mice and induced differentiation for 4 weeks. After the purity identification, BMMCs were contacted by homogeneous microbubbles with the diameter of 1 mm for 1 h. β‐hexosaminidase and histamine levels in supernatants were assessed by enzyme‐linked immunosorbent assay (ELISA) and the CD63 expression was tested by flow cytometry. The intracellular calcium binding with Fluo‐4 AM dyes in BMMCs was observed under the fluorescence microscope and the mean fluorescence intensity was quantitatively measured by flow cytometry. β‐hexosaminidase release, histamine concentration, CD63 expression and calcium influx were significantly increased in BMMCs group upon microbubble stimulation compared to the control groups. After preconditioning with the available inhibitors and microbubble contact, only transient receptor potential vanilloid 1 (TRPV1) and TRPV4 inhibitors robustly suppressed the microbubble‐induced degranulation. Likewise, the elevated fluorescence intensity of cytosolic calcium level was also significantly weaken. The results demonstrated microbubble stimulus effectively promoted BMMCs degranulation, which could be substantially restrained by inhibitors targeted for blocking TRPV1 or TRPV4 channel. The alternation of intracellular calcium level in BMMCs was consistent with the changes of degranulation capacity. It's suggested that the activation of BMMCs by microbubbles may involve specific TRP calcium dependent channels.
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spelling pubmed-106606212023-09-07 The involvement of transient receptor potential channels in mast cell activation by microbubbles Liu, Jia Qing, Long He, Yufei Zhu, Qihui Xu, Weigang Wu, Jianhua J Cell Mol Med Original Articles This study was to explore the activation of mast cells by microbubbles, with the focus on transient receptor potential (TRP) channels mediated degranulation and calcium influx. Bone marrow‐derived mast cells (BMMCs) were primarily obtained from femurs in mice and induced differentiation for 4 weeks. After the purity identification, BMMCs were contacted by homogeneous microbubbles with the diameter of 1 mm for 1 h. β‐hexosaminidase and histamine levels in supernatants were assessed by enzyme‐linked immunosorbent assay (ELISA) and the CD63 expression was tested by flow cytometry. The intracellular calcium binding with Fluo‐4 AM dyes in BMMCs was observed under the fluorescence microscope and the mean fluorescence intensity was quantitatively measured by flow cytometry. β‐hexosaminidase release, histamine concentration, CD63 expression and calcium influx were significantly increased in BMMCs group upon microbubble stimulation compared to the control groups. After preconditioning with the available inhibitors and microbubble contact, only transient receptor potential vanilloid 1 (TRPV1) and TRPV4 inhibitors robustly suppressed the microbubble‐induced degranulation. Likewise, the elevated fluorescence intensity of cytosolic calcium level was also significantly weaken. The results demonstrated microbubble stimulus effectively promoted BMMCs degranulation, which could be substantially restrained by inhibitors targeted for blocking TRPV1 or TRPV4 channel. The alternation of intracellular calcium level in BMMCs was consistent with the changes of degranulation capacity. It's suggested that the activation of BMMCs by microbubbles may involve specific TRP calcium dependent channels. John Wiley and Sons Inc. 2023-09-07 /pmc/articles/PMC10660621/ /pubmed/37680043 http://dx.doi.org/10.1111/jcmm.17947 Text en © 2023 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Liu, Jia
Qing, Long
He, Yufei
Zhu, Qihui
Xu, Weigang
Wu, Jianhua
The involvement of transient receptor potential channels in mast cell activation by microbubbles
title The involvement of transient receptor potential channels in mast cell activation by microbubbles
title_full The involvement of transient receptor potential channels in mast cell activation by microbubbles
title_fullStr The involvement of transient receptor potential channels in mast cell activation by microbubbles
title_full_unstemmed The involvement of transient receptor potential channels in mast cell activation by microbubbles
title_short The involvement of transient receptor potential channels in mast cell activation by microbubbles
title_sort involvement of transient receptor potential channels in mast cell activation by microbubbles
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10660621/
https://www.ncbi.nlm.nih.gov/pubmed/37680043
http://dx.doi.org/10.1111/jcmm.17947
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