Role of SHIP-1 in the adaptive immune responses to aeroallergen in the airway

Background: Th2-dominated inflammatory response in the airway is an integral component in the pathogenesis of allergic asthma. Accumulating evidence supports the notion that the phosphoinositide 3-kinase (PI3K) pathway is involved in the process. We previously reported that SHIP-1, a negative regula...

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Main Authors: Sukit Roongapinun, Sun Young Oh, Fan Wu, Ampai Panthong, Tao Zheng, Zhou Zhu
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/50405
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spelling th-cmuir.6653943832-504052018-09-04T04:41:52Z Role of SHIP-1 in the adaptive immune responses to aeroallergen in the airway Sukit Roongapinun Sun Young Oh Fan Wu Ampai Panthong Tao Zheng Zhou Zhu Agricultural and Biological Sciences Biochemistry, Genetics and Molecular Biology Background: Th2-dominated inflammatory response in the airway is an integral component in the pathogenesis of allergic asthma. Accumulating evidence supports the notion that the phosphoinositide 3-kinase (PI3K) pathway is involved in the process. We previously reported that SHIP-1, a negative regulator of the PI3K pathway, is essential in maintaining lung immunohomeostasis, potentially through regulation of innate immune cells. However, the function of SHIP-1 in adaptive immune response in the lung has not been defined. We sought to determine the role of SHIP-1 in adaptive immunity in response to aeroallergen stimulation in the airway. Methodology/Principal Findings: SHIP-1 knockout (SHIP-1-/-) mice on BALB/c background were immunized with ovalbumin (OVA) plus aluminum hydroxide, a strong Th2-inducing immunization, and challenged with OVA. Airway and lung inflammation, immunoglobulin response, Th2 cytokine production and lymphocyte response were analyzed and compared with wild type mice. Even though there was mild spontaneous inflammation in the lung at baseline, SHIP-1-/-mice showed altered responses, including less cell infiltration around the airways but more in the parenchyma, less mucus production, decreased Th2 cytokine production, and diminished serum OVA-specific IgE, IgG1, but not IgG2a. Nai{dotless}̈ve and OVA sensitized SHIP-1-/-T cells produced a lower amount of IL-4. In vitro differentiated SHIP-1-/-Th2 cells produced less IL-4 compared to wild type Th2 cells upon T cell receptor stimulation. Conclusions/Significance: These findings indicate that, in contrast to its role as a negative regulator in the innate immune cells, SHIP-1 acts as a positive regulator in Th2 cells in the adaptive immune response to aeroallergen. Thus any potential manipulation of SHIP-1 activity should be adjusted according to the specific immune response. © 2010 Roongapinun et al. 2018-09-04T04:40:44Z 2018-09-04T04:40:44Z 2010-12-10 Journal 19326203 2-s2.0-78649789126 10.1371/journal.pone.0014174 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78649789126&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/50405
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Agricultural and Biological Sciences
Biochemistry, Genetics and Molecular Biology
spellingShingle Agricultural and Biological Sciences
Biochemistry, Genetics and Molecular Biology
Sukit Roongapinun
Sun Young Oh
Fan Wu
Ampai Panthong
Tao Zheng
Zhou Zhu
Role of SHIP-1 in the adaptive immune responses to aeroallergen in the airway
description Background: Th2-dominated inflammatory response in the airway is an integral component in the pathogenesis of allergic asthma. Accumulating evidence supports the notion that the phosphoinositide 3-kinase (PI3K) pathway is involved in the process. We previously reported that SHIP-1, a negative regulator of the PI3K pathway, is essential in maintaining lung immunohomeostasis, potentially through regulation of innate immune cells. However, the function of SHIP-1 in adaptive immune response in the lung has not been defined. We sought to determine the role of SHIP-1 in adaptive immunity in response to aeroallergen stimulation in the airway. Methodology/Principal Findings: SHIP-1 knockout (SHIP-1-/-) mice on BALB/c background were immunized with ovalbumin (OVA) plus aluminum hydroxide, a strong Th2-inducing immunization, and challenged with OVA. Airway and lung inflammation, immunoglobulin response, Th2 cytokine production and lymphocyte response were analyzed and compared with wild type mice. Even though there was mild spontaneous inflammation in the lung at baseline, SHIP-1-/-mice showed altered responses, including less cell infiltration around the airways but more in the parenchyma, less mucus production, decreased Th2 cytokine production, and diminished serum OVA-specific IgE, IgG1, but not IgG2a. Nai{dotless}̈ve and OVA sensitized SHIP-1-/-T cells produced a lower amount of IL-4. In vitro differentiated SHIP-1-/-Th2 cells produced less IL-4 compared to wild type Th2 cells upon T cell receptor stimulation. Conclusions/Significance: These findings indicate that, in contrast to its role as a negative regulator in the innate immune cells, SHIP-1 acts as a positive regulator in Th2 cells in the adaptive immune response to aeroallergen. Thus any potential manipulation of SHIP-1 activity should be adjusted according to the specific immune response. © 2010 Roongapinun et al.
format Journal
author Sukit Roongapinun
Sun Young Oh
Fan Wu
Ampai Panthong
Tao Zheng
Zhou Zhu
author_facet Sukit Roongapinun
Sun Young Oh
Fan Wu
Ampai Panthong
Tao Zheng
Zhou Zhu
author_sort Sukit Roongapinun
title Role of SHIP-1 in the adaptive immune responses to aeroallergen in the airway
title_short Role of SHIP-1 in the adaptive immune responses to aeroallergen in the airway
title_full Role of SHIP-1 in the adaptive immune responses to aeroallergen in the airway
title_fullStr Role of SHIP-1 in the adaptive immune responses to aeroallergen in the airway
title_full_unstemmed Role of SHIP-1 in the adaptive immune responses to aeroallergen in the airway
title_sort role of ship-1 in the adaptive immune responses to aeroallergen in the airway
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78649789126&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/50405
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