NOTCH3 contributes to rhinovirus-induced goblet cell hyperplasia in COPD airway epithelial cells
Y Jing, JA Gimenes, R Mishra, D Pham, AT Comstock… - Thorax, 2019 - thorax.bmj.com
Y Jing, JA Gimenes, R Mishra, D Pham, AT Comstock, D Yu, U Sajjan
Thorax, 2019•thorax.bmj.comRationale Goblet cell hyperplasia (GCH) is one of the cardinal features of chronic obstructive
pulmonary disease (COPD) and contributes to airways obstruction. Rhinovirus (RV), which
causes acute exacerbations in patients with COPD, also causes prolonged airways
obstruction. Previously, we showed that RV enhances mucin gene expression and
increases goblet cell number in a COPD mouse model. This study examines whether RV
causes sustained GCH in relevant models of COPD. Methods Mucociliary-differentiated …
pulmonary disease (COPD) and contributes to airways obstruction. Rhinovirus (RV), which
causes acute exacerbations in patients with COPD, also causes prolonged airways
obstruction. Previously, we showed that RV enhances mucin gene expression and
increases goblet cell number in a COPD mouse model. This study examines whether RV
causes sustained GCH in relevant models of COPD. Methods Mucociliary-differentiated …
Rationale
Goblet cell hyperplasia (GCH) is one of the cardinal features of chronic obstructive pulmonary disease (COPD) and contributes to airways obstruction. Rhinovirus (RV), which causes acute exacerbations in patients with COPD, also causes prolonged airways obstruction. Previously, we showed that RV enhances mucin gene expression and increases goblet cell number in a COPD mouse model. This study examines whether RV causes sustained GCH in relevant models of COPD.
Methods
Mucociliary-differentiated COPD and normal airway epithelial cell cultures and mice with normal or COPD phenotype were infected with RV or sham and examined for GCH by immunofluorescence and/or mucin gene expression. In some experiments, RV-infected COPD cells and mice with COPD phenotype were treated with γ-secretase inhibitor or interleukin-13 neutralising antibody and assessed for GCH. To determine the contribution of NOTCH1/3 in RV-induced GCH, COPD cells transduced with NOTCH1/3 shRNA were used.
Results
RV-infected COPD, but not normal cell cultures, showed sustained GCH and increased mucin genes expression. Microarray analysis indicated increased expression of NOTCH1, NOTCH3 and HEY1 only in RV-infected COPD cells. Blocking NOTCH3, but not NOTCH1, attenuated RV-induced GCH in vitro. Inhibition of NOTCH signalling by γ-secretase inhibitor, but not neutralising antibody to IL-13, abrogated RV-induced GCH and mucin gene expression.
Conclusions
RV induces sustained GCH via NOTCH3 particularly in COPD cells or mice with COPD phenotype. This may be one of the mechanisms that may contribute to RV-induced prolonged airways obstruction in COPD.
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