Unknown

Dataset Information

0

Abrogation of airway hyperresponsiveness but not inflammation by rho kinase insufficiency.


ABSTRACT: BACKGROUND:Major features of allergic asthma include airway hyperresponsiveness (AHR), eosinophilic inflammation, and goblet cell metaplasia. Rho kinase (ROCK) is a serine/threonine protein kinase that regulates the actin cytoskeleton. By doing so, it can modulate airway smooth muscle cell contraction and leucocyte migration and proliferation. This study was designed to determine the contributions of the two ROCK isoforms, ROCK1 and ROCK2, to AHR, inflammation and goblet cell metaplasia in a mast cell-dependent model of allergic airways disease. METHODS AND RESULTS:Repeated intranasal challenges with OVA caused AHR, eosinophilic inflammation, and goblet cell hyperplasia in wild-type (WT) mice. OVA-induced AHR was partially or completely abrogated in mice haploinsufficient for ROCK2 (ROCK2(+/-) ) or ROCK1 (ROCK1(+/-) ), respectively. In contrast, there was no effect of ROCK insufficiency on allergic airways inflammation, although both ROCK1 and ROCK2 insufficiency attenuated mast cell degranulation. Goblet cell hyperplasia, as indicated by PAS staining, was not different in ROCK1(+/-) vs. WT mice. However, in ROCK2(+/-) mice, goblet cell hyperplasia was reduced in medium but not large airways. Maximal acetylcholine-induced force generation was reduced in tracheal rings from ROCK1(+/-) and ROCK2(+/-) vs. WT mice. The ROCK inhibitor, fasudil, also reduced airway responsiveness in OVA-challenged mice, without affecting inflammatory responses. CONCLUSION:In a mast cell model of allergic airways disease, ROCK1 and ROCK2 both contribute to AHR, likely through direct effects on smooth muscle cell and effects on mast cell degranulation. In addition, ROCK2 but not ROCK1 plays a role in allergen-induced goblet cell hyperplasia.

SUBMITTER: Kasahara DI 

PROVIDER: S-EPMC4568824 | biostudies-literature | 2015 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

Abrogation of airway hyperresponsiveness but not inflammation by rho kinase insufficiency.

Kasahara David I DI   Ninin Fernanda M C FM   Wurmbrand Alison P AP   Liao James K JK   Shore Stephanie A SA  

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 20150201 2


<h4>Background</h4>Major features of allergic asthma include airway hyperresponsiveness (AHR), eosinophilic inflammation, and goblet cell metaplasia. Rho kinase (ROCK) is a serine/threonine protein kinase that regulates the actin cytoskeleton. By doing so, it can modulate airway smooth muscle cell contraction and leucocyte migration and proliferation. This study was designed to determine the contributions of the two ROCK isoforms, ROCK1 and ROCK2, to AHR, inflammation and goblet cell metaplasia  ...[more]

Similar Datasets

| S-EPMC5070102 | biostudies-literature
| S-EPMC6996596 | biostudies-literature
| S-EPMC3359953 | biostudies-literature
| S-EPMC2914527 | biostudies-other
| S-EPMC2361423 | biostudies-literature
| S-EPMC4233295 | biostudies-literature
| S-EPMC2117268 | biostudies-literature
2005-08-24 | GSE3183 | GEO
2005-08-24 | GSE3184 | GEO
| S-EPMC4725057 | biostudies-literature