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An Essential Regulatory Role of Downstream of Kinase-1 in the Ovalbumin-Induced Murine Model of Asthma

The downstream of kinase (DOK)-1 is involved in the protein tyrosine kinase (PTK) pathway in mast cells, but the role of DOK-1 in the pathogenesis of asthma has not been defined. In this study, we have demonstrated a novel regulatory role of DOK-1 in airway inflammation and physiologic responses in...

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Autores principales: Lee, Chang-Min, Jung, In Duk, Noh, Kyung Tae, Lee, Jun Sik, Park, Jin Wook, Heo, Deok Rim, Park, Jun Ho, Chang, Jeong Hyun, Choi, Il-Whan, Kim, Jong-Suk, Shin, Yong Kyoo, Park, Sung-Joo, Han, Myung-Kwan, Lee, Chun Geun, Cho, Won-Kyung, Park, Yeong-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326039/
https://www.ncbi.nlm.nih.gov/pubmed/22514638
http://dx.doi.org/10.1371/journal.pone.0034554
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author Lee, Chang-Min
Jung, In Duk
Noh, Kyung Tae
Lee, Jun Sik
Park, Jin Wook
Heo, Deok Rim
Park, Jun Ho
Chang, Jeong Hyun
Choi, Il-Whan
Kim, Jong-Suk
Shin, Yong Kyoo
Park, Sung-Joo
Han, Myung-Kwan
Lee, Chun Geun
Cho, Won-Kyung
Park, Yeong-Min
author_facet Lee, Chang-Min
Jung, In Duk
Noh, Kyung Tae
Lee, Jun Sik
Park, Jin Wook
Heo, Deok Rim
Park, Jun Ho
Chang, Jeong Hyun
Choi, Il-Whan
Kim, Jong-Suk
Shin, Yong Kyoo
Park, Sung-Joo
Han, Myung-Kwan
Lee, Chun Geun
Cho, Won-Kyung
Park, Yeong-Min
author_sort Lee, Chang-Min
collection PubMed
description The downstream of kinase (DOK)-1 is involved in the protein tyrosine kinase (PTK) pathway in mast cells, but the role of DOK-1 in the pathogenesis of asthma has not been defined. In this study, we have demonstrated a novel regulatory role of DOK-1 in airway inflammation and physiologic responses in a murine model of asthma using lentiviral vector containing DOK-1 cDNA or DOK-1-specific ShRNA. The OVA-induced inflammatory cells, airway hyperresponsiveness, Th2 cytokine expression, and mucus response were significantly reduced in DOK-1 overexpressing mice compared to OVA-challenged control mice. The transgenic introduction of DOK-1 significantly stimulated the activation and expression of STAT-4 and T-bet, while impressively inhibiting the activation and expression of STAT-6 and GATA-3 in airway epithelial cells. On the other hand, DOK-1 knockdown mice enhanced STAT-6 expression and its nuclear translocation compared to OVA-challenged control mice. When viewed in combination, our studies demonstrate DOK-1 regulates allergen-induced Th2 immune responses by selective stimulation and inhibition of STAT-4 and STAT-6 signaling pathways, respectively. These studies provide a novel insight on the regulatory role of DOK-1 in allergen-induced Th2 inflammation and airway responses, which has therapeutic potential for asthma and other allergic diseases.
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spelling pubmed-33260392012-04-18 An Essential Regulatory Role of Downstream of Kinase-1 in the Ovalbumin-Induced Murine Model of Asthma Lee, Chang-Min Jung, In Duk Noh, Kyung Tae Lee, Jun Sik Park, Jin Wook Heo, Deok Rim Park, Jun Ho Chang, Jeong Hyun Choi, Il-Whan Kim, Jong-Suk Shin, Yong Kyoo Park, Sung-Joo Han, Myung-Kwan Lee, Chun Geun Cho, Won-Kyung Park, Yeong-Min PLoS One Research Article The downstream of kinase (DOK)-1 is involved in the protein tyrosine kinase (PTK) pathway in mast cells, but the role of DOK-1 in the pathogenesis of asthma has not been defined. In this study, we have demonstrated a novel regulatory role of DOK-1 in airway inflammation and physiologic responses in a murine model of asthma using lentiviral vector containing DOK-1 cDNA or DOK-1-specific ShRNA. The OVA-induced inflammatory cells, airway hyperresponsiveness, Th2 cytokine expression, and mucus response were significantly reduced in DOK-1 overexpressing mice compared to OVA-challenged control mice. The transgenic introduction of DOK-1 significantly stimulated the activation and expression of STAT-4 and T-bet, while impressively inhibiting the activation and expression of STAT-6 and GATA-3 in airway epithelial cells. On the other hand, DOK-1 knockdown mice enhanced STAT-6 expression and its nuclear translocation compared to OVA-challenged control mice. When viewed in combination, our studies demonstrate DOK-1 regulates allergen-induced Th2 immune responses by selective stimulation and inhibition of STAT-4 and STAT-6 signaling pathways, respectively. These studies provide a novel insight on the regulatory role of DOK-1 in allergen-induced Th2 inflammation and airway responses, which has therapeutic potential for asthma and other allergic diseases. Public Library of Science 2012-04-13 /pmc/articles/PMC3326039/ /pubmed/22514638 http://dx.doi.org/10.1371/journal.pone.0034554 Text en Lee et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lee, Chang-Min
Jung, In Duk
Noh, Kyung Tae
Lee, Jun Sik
Park, Jin Wook
Heo, Deok Rim
Park, Jun Ho
Chang, Jeong Hyun
Choi, Il-Whan
Kim, Jong-Suk
Shin, Yong Kyoo
Park, Sung-Joo
Han, Myung-Kwan
Lee, Chun Geun
Cho, Won-Kyung
Park, Yeong-Min
An Essential Regulatory Role of Downstream of Kinase-1 in the Ovalbumin-Induced Murine Model of Asthma
title An Essential Regulatory Role of Downstream of Kinase-1 in the Ovalbumin-Induced Murine Model of Asthma
title_full An Essential Regulatory Role of Downstream of Kinase-1 in the Ovalbumin-Induced Murine Model of Asthma
title_fullStr An Essential Regulatory Role of Downstream of Kinase-1 in the Ovalbumin-Induced Murine Model of Asthma
title_full_unstemmed An Essential Regulatory Role of Downstream of Kinase-1 in the Ovalbumin-Induced Murine Model of Asthma
title_short An Essential Regulatory Role of Downstream of Kinase-1 in the Ovalbumin-Induced Murine Model of Asthma
title_sort essential regulatory role of downstream of kinase-1 in the ovalbumin-induced murine model of asthma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326039/
https://www.ncbi.nlm.nih.gov/pubmed/22514638
http://dx.doi.org/10.1371/journal.pone.0034554
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