Cargando…

Ceramide Nanoliposomes as Potential Therapeutic Reagents for Asthma

Ceramides are an emerging class of anti-inflammatory lipids, and nanoscale ceramide-delivery systems are potential therapeutic strategies for inflammatory diseases. This study investigated the therapeutic effects of ceramide nanoliposomes (CNL) on type 2 inflammation-based asthma, induced by repeate...

Descripción completa

Detalles Bibliográficos
Autores principales: Sakae, Harumi, Ogiso, Yuri, Matsuda, Masaya, Shimora, Hayato, Deering, Tye, Fox, Todd E., Kester, Mark, Nabe, Takeshi, Kitatani, Kazuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954069/
https://www.ncbi.nlm.nih.gov/pubmed/36831258
http://dx.doi.org/10.3390/cells12040591
_version_ 1784894035273449472
author Sakae, Harumi
Ogiso, Yuri
Matsuda, Masaya
Shimora, Hayato
Deering, Tye
Fox, Todd E.
Kester, Mark
Nabe, Takeshi
Kitatani, Kazuyuki
author_facet Sakae, Harumi
Ogiso, Yuri
Matsuda, Masaya
Shimora, Hayato
Deering, Tye
Fox, Todd E.
Kester, Mark
Nabe, Takeshi
Kitatani, Kazuyuki
author_sort Sakae, Harumi
collection PubMed
description Ceramides are an emerging class of anti-inflammatory lipids, and nanoscale ceramide-delivery systems are potential therapeutic strategies for inflammatory diseases. This study investigated the therapeutic effects of ceramide nanoliposomes (CNL) on type 2 inflammation-based asthma, induced by repeated ovalbumin (OVA) challenges. Asthmatic mice intratracheally treated with ceramide-free liposomes (Ghost) displayed typical airway remodeling including mucosal accumulation and subepithelial fibrosis, whereas, in CNL-treated mice, the degree of airway remodeling was significantly decreased. Compared to the Ghost group, CNL treatment unexpectedly failed to significantly influence formation of type 2 cytokines, including IL-5 and IL-13, known to facilitate pathogenic production of airway mucus predominantly comprising MUC5AC mucin. Interestingly, CNL treatment suppressed OVA-evoked hyperplasia of MUC5AC-generating goblet cells in the airways. This suggests that CNL suppressed goblet cell hyperplasia and airway mucosal accumulation independently of type 2 cytokine formation. Mechanistically, CNL treatment suppressed cell growth and EGF-induced activation of Akt, but not ERK1/2, in a human lung epithelial cell culture system recapitulating airway goblet cell hyperplasia. Taken together, CNL is suggested to have therapeutic effects on airway remodeling in allergic asthma by targeting goblet cell hyperplasia. These findings raise the potential of ceramide-based therapies for airway diseases, such as asthma.
format Online
Article
Text
id pubmed-9954069
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-99540692023-02-25 Ceramide Nanoliposomes as Potential Therapeutic Reagents for Asthma Sakae, Harumi Ogiso, Yuri Matsuda, Masaya Shimora, Hayato Deering, Tye Fox, Todd E. Kester, Mark Nabe, Takeshi Kitatani, Kazuyuki Cells Article Ceramides are an emerging class of anti-inflammatory lipids, and nanoscale ceramide-delivery systems are potential therapeutic strategies for inflammatory diseases. This study investigated the therapeutic effects of ceramide nanoliposomes (CNL) on type 2 inflammation-based asthma, induced by repeated ovalbumin (OVA) challenges. Asthmatic mice intratracheally treated with ceramide-free liposomes (Ghost) displayed typical airway remodeling including mucosal accumulation and subepithelial fibrosis, whereas, in CNL-treated mice, the degree of airway remodeling was significantly decreased. Compared to the Ghost group, CNL treatment unexpectedly failed to significantly influence formation of type 2 cytokines, including IL-5 and IL-13, known to facilitate pathogenic production of airway mucus predominantly comprising MUC5AC mucin. Interestingly, CNL treatment suppressed OVA-evoked hyperplasia of MUC5AC-generating goblet cells in the airways. This suggests that CNL suppressed goblet cell hyperplasia and airway mucosal accumulation independently of type 2 cytokine formation. Mechanistically, CNL treatment suppressed cell growth and EGF-induced activation of Akt, but not ERK1/2, in a human lung epithelial cell culture system recapitulating airway goblet cell hyperplasia. Taken together, CNL is suggested to have therapeutic effects on airway remodeling in allergic asthma by targeting goblet cell hyperplasia. These findings raise the potential of ceramide-based therapies for airway diseases, such as asthma. MDPI 2023-02-11 /pmc/articles/PMC9954069/ /pubmed/36831258 http://dx.doi.org/10.3390/cells12040591 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sakae, Harumi
Ogiso, Yuri
Matsuda, Masaya
Shimora, Hayato
Deering, Tye
Fox, Todd E.
Kester, Mark
Nabe, Takeshi
Kitatani, Kazuyuki
Ceramide Nanoliposomes as Potential Therapeutic Reagents for Asthma
title Ceramide Nanoliposomes as Potential Therapeutic Reagents for Asthma
title_full Ceramide Nanoliposomes as Potential Therapeutic Reagents for Asthma
title_fullStr Ceramide Nanoliposomes as Potential Therapeutic Reagents for Asthma
title_full_unstemmed Ceramide Nanoliposomes as Potential Therapeutic Reagents for Asthma
title_short Ceramide Nanoliposomes as Potential Therapeutic Reagents for Asthma
title_sort ceramide nanoliposomes as potential therapeutic reagents for asthma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954069/
https://www.ncbi.nlm.nih.gov/pubmed/36831258
http://dx.doi.org/10.3390/cells12040591
work_keys_str_mv AT sakaeharumi ceramidenanoliposomesaspotentialtherapeuticreagentsforasthma
AT ogisoyuri ceramidenanoliposomesaspotentialtherapeuticreagentsforasthma
AT matsudamasaya ceramidenanoliposomesaspotentialtherapeuticreagentsforasthma
AT shimorahayato ceramidenanoliposomesaspotentialtherapeuticreagentsforasthma
AT deeringtye ceramidenanoliposomesaspotentialtherapeuticreagentsforasthma
AT foxtodde ceramidenanoliposomesaspotentialtherapeuticreagentsforasthma
AT kestermark ceramidenanoliposomesaspotentialtherapeuticreagentsforasthma
AT nabetakeshi ceramidenanoliposomesaspotentialtherapeuticreagentsforasthma
AT kitatanikazuyuki ceramidenanoliposomesaspotentialtherapeuticreagentsforasthma