Airway epithelial cell-derived insulin-like growth factor-1 triggers skewed CD8+ T cell polarization

Skewed CD8+ T cell responses are important in airway inflammation. This study investigates the role of the airway epithelial cell‐derived insulin‐like growth factor 1 (IGF1) in contributing to CD8+ T cell polarization. Expression of IGF1 in the airway epithelial cell line, RPMI2650 cells, was assess...

Full description

Saved in:
Bibliographic Details
Published inCell biology international Vol. 38; no. 10; pp. 1148 - 1154
Main Authors Zou, Jian-Yong, Huang, Shao-hong, Li, Yun, Chen, Hui-guo, Rong, Jian, Ye, Sheng
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.10.2014
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Skewed CD8+ T cell responses are important in airway inflammation. This study investigates the role of the airway epithelial cell‐derived insulin‐like growth factor 1 (IGF1) in contributing to CD8+ T cell polarization. Expression of IGF1 in the airway epithelial cell line, RPMI2650 cells, was assessed by quantitative real time RT‐PCR and Western blotting. The role of IGF1 in regulating CD8+ T cell activation was observed by coculture of mite allergen‐primed RPMI2650 cells and naïve CD8+ T cells. CD8+ T cell polarization was assessed by the carboxyfluorescein succinimidyl ester‐dilution assay and the determination of cytotoxic cytokine levels in the culture medium. Exposure to mite allergen, Der p1, increased the expression of IGF1 by RPMI2650 cells. The epithelial cell‐derived IGF1 prevented the activation‐induced cell death by inducing the p53 gene hypermethylation. Mite allergen‐primed RPMI2650 cells induced an antigen‐specific CD8+ T cell polarization. We conclude that mite allergens induce airway epithelial cell line, RPMI2650 cells, to produce IGF1; the latter contributes to antigen‐specific CD8+ T cell polarization.
Bibliography:ark:/67375/WNG-M43X4GRF-K
Guangdong Natural Science Foundation - No. 10451008901005515; No. 10151008901000177
istex:EA264B2FD750505E3C1D8AB860B3FCD63507B35D
ArticleID:CBIN10313
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1065-6995
1095-8355
DOI:10.1002/cbin.10313