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TRPV4 promotes acoustic wave-mediated BBB opening via Ca(2+)/PKC-δ pathway
INTRODUCTION: Numerous studies have shown the ability of low-energy acoustic waves such as focused ultrasound or shockwave to transiently open blood-brain barrier (BBB) and facilitate drug delivery to the brain. Preclinical and clinical evidences have well demonstrated the efficacy and safety in tre...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584681/ https://www.ncbi.nlm.nih.gov/pubmed/33133680 http://dx.doi.org/10.1016/j.jare.2020.06.012 |
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author | Liao, Wei-Hao Hsiao, Ming-Yen Kung, Yi Liu, Hao-Li Béra, Jean-Christophe Inserra, Claude Chen, Wen-Shiang |
author_facet | Liao, Wei-Hao Hsiao, Ming-Yen Kung, Yi Liu, Hao-Li Béra, Jean-Christophe Inserra, Claude Chen, Wen-Shiang |
author_sort | Liao, Wei-Hao |
collection | PubMed |
description | INTRODUCTION: Numerous studies have shown the ability of low-energy acoustic waves such as focused ultrasound or shockwave to transiently open blood-brain barrier (BBB) and facilitate drug delivery to the brain. Preclinical and clinical evidences have well demonstrated the efficacy and safety in treating various brain disorders. However, the molecular mechanisms of acoustic waves on the BBB are still not fully understood. OBJECTIVES: The present study aimed at exploring the possible molecular mechanisms of acoustic wave stimulation on brains. METHODS: BRIEFLY DESCRIBE THE EXPERIMENTAL DESIGN: The left hemisphere of the rat‘s brain was treated with pulsed ultrasound from a commercial focused shockwave or a planar ultrasound device, and the right hemisphere served as a control. One hour after the mechanical wave stimulation or overnight, the rats were sacrificed and the brains were harvested for protein or histological analysis. Agonists and antagonists related to the signal transduction pathways of tight junction proteins were used to investigate the possible intracellular mechanisms. RESULTS: Intracellular signal transduction analysis shows calcium influx through transient receptor potential vanilloid 4 (TRPV4) channels, and the activation of PKC-δ pathway to mediate dissociation of ZO-1 and occludin after acoustic wave stimulation. The activation of TRPV4 or PKC-δ signaling further increased the expression level of TRPV4, suggesting a feedback loop to regulate BBB permeability. Moreover, the tight junction proteins dissociation can be reversed by administration of PKC-δ inhibitor and TRPV4 antagonist. CONCLUSION: The present study shows the crucial role of TRPV4 in acoustic wave-mediated BBB permeability, specifically its effect on compromising tight junction proteins, ZO-1 and occludin. Our findings provide a new molecular perspective to explain acoustic wave-mediated BBB opening. Moreover, activation of TRPV4 by agonists may reduce the threshold intensity level of acoustic waves for BBB opening, which may prevent undesirable mechanical damages while maintaining efficient BBB opening. |
format | Online Article Text |
id | pubmed-7584681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75846812020-10-30 TRPV4 promotes acoustic wave-mediated BBB opening via Ca(2+)/PKC-δ pathway Liao, Wei-Hao Hsiao, Ming-Yen Kung, Yi Liu, Hao-Li Béra, Jean-Christophe Inserra, Claude Chen, Wen-Shiang J Adv Res Article INTRODUCTION: Numerous studies have shown the ability of low-energy acoustic waves such as focused ultrasound or shockwave to transiently open blood-brain barrier (BBB) and facilitate drug delivery to the brain. Preclinical and clinical evidences have well demonstrated the efficacy and safety in treating various brain disorders. However, the molecular mechanisms of acoustic waves on the BBB are still not fully understood. OBJECTIVES: The present study aimed at exploring the possible molecular mechanisms of acoustic wave stimulation on brains. METHODS: BRIEFLY DESCRIBE THE EXPERIMENTAL DESIGN: The left hemisphere of the rat‘s brain was treated with pulsed ultrasound from a commercial focused shockwave or a planar ultrasound device, and the right hemisphere served as a control. One hour after the mechanical wave stimulation or overnight, the rats were sacrificed and the brains were harvested for protein or histological analysis. Agonists and antagonists related to the signal transduction pathways of tight junction proteins were used to investigate the possible intracellular mechanisms. RESULTS: Intracellular signal transduction analysis shows calcium influx through transient receptor potential vanilloid 4 (TRPV4) channels, and the activation of PKC-δ pathway to mediate dissociation of ZO-1 and occludin after acoustic wave stimulation. The activation of TRPV4 or PKC-δ signaling further increased the expression level of TRPV4, suggesting a feedback loop to regulate BBB permeability. Moreover, the tight junction proteins dissociation can be reversed by administration of PKC-δ inhibitor and TRPV4 antagonist. CONCLUSION: The present study shows the crucial role of TRPV4 in acoustic wave-mediated BBB permeability, specifically its effect on compromising tight junction proteins, ZO-1 and occludin. Our findings provide a new molecular perspective to explain acoustic wave-mediated BBB opening. Moreover, activation of TRPV4 by agonists may reduce the threshold intensity level of acoustic waves for BBB opening, which may prevent undesirable mechanical damages while maintaining efficient BBB opening. Elsevier 2020-06-21 /pmc/articles/PMC7584681/ /pubmed/33133680 http://dx.doi.org/10.1016/j.jare.2020.06.012 Text en © 2020 The Authors. Published by Elsevier B.V. on behalf of Cairo University. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Liao, Wei-Hao Hsiao, Ming-Yen Kung, Yi Liu, Hao-Li Béra, Jean-Christophe Inserra, Claude Chen, Wen-Shiang TRPV4 promotes acoustic wave-mediated BBB opening via Ca(2+)/PKC-δ pathway |
title | TRPV4 promotes acoustic wave-mediated BBB opening via Ca(2+)/PKC-δ pathway |
title_full | TRPV4 promotes acoustic wave-mediated BBB opening via Ca(2+)/PKC-δ pathway |
title_fullStr | TRPV4 promotes acoustic wave-mediated BBB opening via Ca(2+)/PKC-δ pathway |
title_full_unstemmed | TRPV4 promotes acoustic wave-mediated BBB opening via Ca(2+)/PKC-δ pathway |
title_short | TRPV4 promotes acoustic wave-mediated BBB opening via Ca(2+)/PKC-δ pathway |
title_sort | trpv4 promotes acoustic wave-mediated bbb opening via ca(2+)/pkc-δ pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584681/ https://www.ncbi.nlm.nih.gov/pubmed/33133680 http://dx.doi.org/10.1016/j.jare.2020.06.012 |
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