Referenced in: none

Automatically associated channels: ClC4

Title: Gob-5 is not essential for mucus overproduction in preclinical murine models of allergic asthma.

Authors: Annette Robichaud, Stephanie A Tuck, Stacia Kargman, John Tam, Elizabeth Wong, Mark Abramovitz, James R Mortimer, James Mortimer, Helen E Burston, Paul Masson, Jeremy Hirota, Deborah Slipetz, Brian Kennedy, Gary O'Neill, Steven Xanthoudakis

Journal, date & volume: Am. J. Respir. Cell Mol. Biol., 2005 Sep , 33, 303-14

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/15947424

Abstract
Overexpression of Gob-5 has previously been linked to goblet cell metaplasia and mucin overproduction in both in vitro and in vivo model systems. In this study, Gob-5 knockout mice were generated and their phenotype was evaluated in two established preclinical models of allergic asthma. We sought to determine whether the Gob-5-null animals could produce less mucus in response to allergic challenge, and whether this would have any impact on reducing goblet cell metaplasia and airway inflammation. We found that in the absence of a proinflammatory stimulus we could not detect an overt phenotypic difference between age and sex-matched knockout and wild-type animals. Allergic challenge with ovalbumin or intranasal administration of interleukin-13 produced a robust allergic response that was similar regardless of genotype. In addition, siRNA-mediated knockdown of CLCA-1 in cultured lung epithelial cells failed to reduce mucin expression in vitro. Thus, in contrast to previously published reports, our findings show that Gob-5 expression is not essential for mucin overproduction in vitro or in murine models of allergic asthma. Furthermore, we have also exploited the use of gene expression array analysis to investigate the possibility that a compensatory mechanism, involving other genes, may act to override the requirement for Gob-5-mediated mucus overproduction.