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Effects of Heat Shock Protein 90 Inhibition In the Lungs

Inhibition of Hsp90 is associated with anti-inflammatory effects. We employed human lung microvascular endothelial cells to investigate the effects of the Hsp90 inhibitors 17-AAG, AUY-922 and 17-DMAG in the unfolded protein response (UPR) and viability of lung cells. Our observations indicate that m...

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Autores principales: Uddin, Mohammad A., Kubra, Khadeja-Tul, Sonju, Jafrin Jobayer, Akhter, Mohammad S., Seetharama, Jois, Barabutis, Nektarios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390472/
https://www.ncbi.nlm.nih.gov/pubmed/32728665
http://dx.doi.org/10.1016/j.medidd.2020.100046
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author Uddin, Mohammad A.
Kubra, Khadeja-Tul
Sonju, Jafrin Jobayer
Akhter, Mohammad S.
Seetharama, Jois
Barabutis, Nektarios
author_facet Uddin, Mohammad A.
Kubra, Khadeja-Tul
Sonju, Jafrin Jobayer
Akhter, Mohammad S.
Seetharama, Jois
Barabutis, Nektarios
author_sort Uddin, Mohammad A.
collection PubMed
description Inhibition of Hsp90 is associated with anti-inflammatory effects. We employed human lung microvascular endothelial cells to investigate the effects of the Hsp90 inhibitors 17-AAG, AUY-922 and 17-DMAG in the unfolded protein response (UPR) and viability of lung cells. Our observations indicate that moderate doses of those compounds trigger the activation of the UPR without inducing lethal effects in vitro. Indeed, AUY-922 triggered UPR activation in the lungs of C57BL/6 mice. UPR has been previously involved in the enhancement of the lung endothelial barrier function. Thus, the present study suggests that the barrier protective effects of Hsp90 inhibition in the lung microvasculature are highly probable to be associated with the activation of the UPR. Hence, the development of novel compounds which stochastically capacitate the repairing elements of UPR, may deliver new therapeutic possibilities against the severities of the acute respiratory distress syndrome.
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spelling pubmed-73904722021-06-01 Effects of Heat Shock Protein 90 Inhibition In the Lungs Uddin, Mohammad A. Kubra, Khadeja-Tul Sonju, Jafrin Jobayer Akhter, Mohammad S. Seetharama, Jois Barabutis, Nektarios Med Drug Discov Article Inhibition of Hsp90 is associated with anti-inflammatory effects. We employed human lung microvascular endothelial cells to investigate the effects of the Hsp90 inhibitors 17-AAG, AUY-922 and 17-DMAG in the unfolded protein response (UPR) and viability of lung cells. Our observations indicate that moderate doses of those compounds trigger the activation of the UPR without inducing lethal effects in vitro. Indeed, AUY-922 triggered UPR activation in the lungs of C57BL/6 mice. UPR has been previously involved in the enhancement of the lung endothelial barrier function. Thus, the present study suggests that the barrier protective effects of Hsp90 inhibition in the lung microvasculature are highly probable to be associated with the activation of the UPR. Hence, the development of novel compounds which stochastically capacitate the repairing elements of UPR, may deliver new therapeutic possibilities against the severities of the acute respiratory distress syndrome. 2020-05-17 2020-06 /pmc/articles/PMC7390472/ /pubmed/32728665 http://dx.doi.org/10.1016/j.medidd.2020.100046 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Uddin, Mohammad A.
Kubra, Khadeja-Tul
Sonju, Jafrin Jobayer
Akhter, Mohammad S.
Seetharama, Jois
Barabutis, Nektarios
Effects of Heat Shock Protein 90 Inhibition In the Lungs
title Effects of Heat Shock Protein 90 Inhibition In the Lungs
title_full Effects of Heat Shock Protein 90 Inhibition In the Lungs
title_fullStr Effects of Heat Shock Protein 90 Inhibition In the Lungs
title_full_unstemmed Effects of Heat Shock Protein 90 Inhibition In the Lungs
title_short Effects of Heat Shock Protein 90 Inhibition In the Lungs
title_sort effects of heat shock protein 90 inhibition in the lungs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390472/
https://www.ncbi.nlm.nih.gov/pubmed/32728665
http://dx.doi.org/10.1016/j.medidd.2020.100046
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