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Hedgehog Signaling as a Therapeutic Target for Airway Remodeling and Inflammation in Allergic Asthma
Genome-wide association studies (GWAS) have shown that variants of patched homolog 1 (PTCH1) are associated with lung function abnormalities in the general population. It has also been shown that sonic hedgehog (SHH), an important ligand for PTCH1, is upregulated in the airway epithelium of patients...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562640/ https://www.ncbi.nlm.nih.gov/pubmed/36230980 http://dx.doi.org/10.3390/cells11193016 |
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author | Tam, Anthony Osei, Emmanuel Twumasi Cheung, Chung Y. Hughes, Michael Yang, Chen X. McNagny, Kelly M. Dorscheid, Delbert R. Singhera, Gurpreet K. Hallstrand, Teal S. Warner, Stephanie Hogg, James C. Hackett, Tillie L. Lim, Chinten J. Sin, Don D. |
author_facet | Tam, Anthony Osei, Emmanuel Twumasi Cheung, Chung Y. Hughes, Michael Yang, Chen X. McNagny, Kelly M. Dorscheid, Delbert R. Singhera, Gurpreet K. Hallstrand, Teal S. Warner, Stephanie Hogg, James C. Hackett, Tillie L. Lim, Chinten J. Sin, Don D. |
author_sort | Tam, Anthony |
collection | PubMed |
description | Genome-wide association studies (GWAS) have shown that variants of patched homolog 1 (PTCH1) are associated with lung function abnormalities in the general population. It has also been shown that sonic hedgehog (SHH), an important ligand for PTCH1, is upregulated in the airway epithelium of patients with asthma and is suggested to be involved in airway remodeling. The contribution of hedgehog signaling to airway remodeling and inflammation in asthma is poorly described. To determine the biological role of hedgehog signaling-associated genes in asthma, gene silencing, over-expression, and pharmacologic inhibition studies were conducted after stimulating human airway epithelial cells or not with transforming growth factor β1 (TGFβ1), an important fibrotic mediator in asthmatic airway remodeling that also interacts with SHH pathway. TGFβ1 increased hedgehog-signaling-related gene expression including SHH, GLI1 and GLI2. Knockdown of PTCH1 or SMO with siRNA, or use of hedgehog signaling inhibitors, consistently attenuated COL1A1 expression induced by TGFβ1 stimulation. In contrast, Ptch1 over-expression augmented TGFβ1-induced an increase in COL1A1 and MMP2 gene expression. We also showed an increase in hedgehog-signaling-related gene expression in primary airway epithelial cells from controls and asthmatics at different stages of cellular differentiation. GANT61, an inhibitor of GLI1/2, attenuated TGFβ1-induced increase in COL1A1 protein expression in primary airway epithelial cells differentiated in air–liquid interface. Finally, to model airway tissue remodeling in vivo, C57BL/6 wildtype (WT) and Ptch1(+/−) mice were intranasally challenged with house dust mite (HDM) or phosphate-buffered saline (PBS) control. Ptch1(+/−) mice showed reduced sub-epithelial collagen expression and serum inflammatory proteins compared to WT mice in response to HDM challenge. In conclusion, TGFβ1-induced airway remodeling is partially mediated through the hedgehog signaling pathway via the PTCH1-SMO-GLI axis. The Hedgehog signaling pathway is a promising new potential therapeutic target to alleviate airway tissue remodeling in patients with allergic airways disease. |
format | Online Article Text |
id | pubmed-9562640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95626402022-10-15 Hedgehog Signaling as a Therapeutic Target for Airway Remodeling and Inflammation in Allergic Asthma Tam, Anthony Osei, Emmanuel Twumasi Cheung, Chung Y. Hughes, Michael Yang, Chen X. McNagny, Kelly M. Dorscheid, Delbert R. Singhera, Gurpreet K. Hallstrand, Teal S. Warner, Stephanie Hogg, James C. Hackett, Tillie L. Lim, Chinten J. Sin, Don D. Cells Article Genome-wide association studies (GWAS) have shown that variants of patched homolog 1 (PTCH1) are associated with lung function abnormalities in the general population. It has also been shown that sonic hedgehog (SHH), an important ligand for PTCH1, is upregulated in the airway epithelium of patients with asthma and is suggested to be involved in airway remodeling. The contribution of hedgehog signaling to airway remodeling and inflammation in asthma is poorly described. To determine the biological role of hedgehog signaling-associated genes in asthma, gene silencing, over-expression, and pharmacologic inhibition studies were conducted after stimulating human airway epithelial cells or not with transforming growth factor β1 (TGFβ1), an important fibrotic mediator in asthmatic airway remodeling that also interacts with SHH pathway. TGFβ1 increased hedgehog-signaling-related gene expression including SHH, GLI1 and GLI2. Knockdown of PTCH1 or SMO with siRNA, or use of hedgehog signaling inhibitors, consistently attenuated COL1A1 expression induced by TGFβ1 stimulation. In contrast, Ptch1 over-expression augmented TGFβ1-induced an increase in COL1A1 and MMP2 gene expression. We also showed an increase in hedgehog-signaling-related gene expression in primary airway epithelial cells from controls and asthmatics at different stages of cellular differentiation. GANT61, an inhibitor of GLI1/2, attenuated TGFβ1-induced increase in COL1A1 protein expression in primary airway epithelial cells differentiated in air–liquid interface. Finally, to model airway tissue remodeling in vivo, C57BL/6 wildtype (WT) and Ptch1(+/−) mice were intranasally challenged with house dust mite (HDM) or phosphate-buffered saline (PBS) control. Ptch1(+/−) mice showed reduced sub-epithelial collagen expression and serum inflammatory proteins compared to WT mice in response to HDM challenge. In conclusion, TGFβ1-induced airway remodeling is partially mediated through the hedgehog signaling pathway via the PTCH1-SMO-GLI axis. The Hedgehog signaling pathway is a promising new potential therapeutic target to alleviate airway tissue remodeling in patients with allergic airways disease. MDPI 2022-09-27 /pmc/articles/PMC9562640/ /pubmed/36230980 http://dx.doi.org/10.3390/cells11193016 Text en © 2022 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 Tam, Anthony Osei, Emmanuel Twumasi Cheung, Chung Y. Hughes, Michael Yang, Chen X. McNagny, Kelly M. Dorscheid, Delbert R. Singhera, Gurpreet K. Hallstrand, Teal S. Warner, Stephanie Hogg, James C. Hackett, Tillie L. Lim, Chinten J. Sin, Don D. Hedgehog Signaling as a Therapeutic Target for Airway Remodeling and Inflammation in Allergic Asthma |
title | Hedgehog Signaling as a Therapeutic Target for Airway Remodeling and Inflammation in Allergic Asthma |
title_full | Hedgehog Signaling as a Therapeutic Target for Airway Remodeling and Inflammation in Allergic Asthma |
title_fullStr | Hedgehog Signaling as a Therapeutic Target for Airway Remodeling and Inflammation in Allergic Asthma |
title_full_unstemmed | Hedgehog Signaling as a Therapeutic Target for Airway Remodeling and Inflammation in Allergic Asthma |
title_short | Hedgehog Signaling as a Therapeutic Target for Airway Remodeling and Inflammation in Allergic Asthma |
title_sort | hedgehog signaling as a therapeutic target for airway remodeling and inflammation in allergic asthma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562640/ https://www.ncbi.nlm.nih.gov/pubmed/36230980 http://dx.doi.org/10.3390/cells11193016 |
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