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IL-13–induced airway mucus production is attenuated by MAPK13 inhibition
Yael G. Alevy, … , Tom J. Brett, Michael J. Holtzman
Yael G. Alevy, … , Tom J. Brett, Michael J. Holtzman
Published November 26, 2012
Citation Information: J Clin Invest. 2012;122(12):4555-4568. https://doi.org/10.1172/JCI64896.
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Research Article

IL-13–induced airway mucus production is attenuated by MAPK13 inhibition

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Abstract

Increased mucus production is a common cause of morbidity and mortality in inflammatory airway diseases, including asthma, chronic obstructive pulmonary disease (COPD), and cystic fibrosis. However, the precise molecular mechanisms for pathogenic mucus production are largely undetermined. Accordingly, there are no specific and effective anti-mucus therapeutics. Here, we define a signaling pathway from chloride channel calcium-activated 1 (CLCA1) to MAPK13 that is responsible for IL-13–driven mucus production in human airway epithelial cells. The same pathway was also highly activated in the lungs of humans with excess mucus production due to COPD. We further validated the pathway by using structure-based drug design to develop a series of novel MAPK13 inhibitors with nanomolar potency that effectively reduced mucus production in human airway epithelial cells. These results uncover and validate a new pathway for regulating mucus production as well as a corresponding therapeutic approach to mucus overproduction in inflammatory airway diseases.

Authors

Yael G. Alevy, Anand C. Patel, Arthur G. Romero, Dhara A. Patel, Jennifer Tucker, William T. Roswit, Chantel A. Miller, Richard F. Heier, Derek E. Byers, Tom J. Brett, Michael J. Holtzman

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Figure 1

CLCA1 is necessary for IL-13–stimulated mucus production in human airway epithelial cells.

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CLCA1 is necessary for IL-13–stimulated mucus production in human airway...
(A) hTECs were incubated with IL-13 (50 ng/ml) under submerged conditions for 2 days and then air-liquid interface conditions for up to 21 days, and cell lysates were analyzed for CLCA1, CLCA2, and CLCA4 mRNA levels by real-time qPCR assay. CLCA3 mRNA was undetectable under these conditions (data not shown). (B) Corresponding levels of MUC5AC mRNA. (C) Corresponding levels of CLCA1 in cell lysate and apical cell supernatant determined by ELISA. (D) Corresponding levels of MUC5AC determined by ELISA. (E) Corresponding immunocytochemistry for DAPI, CLCA1, and MUC5AC using confocal microscopy. Scale bar: 50 μm. (F) Corresponding immunocytochemistry at a more apical (high z axis) and subjacent (low z axis) cellular location. Arrows indicate the same reference cells for high and low z axis. Scale bar: 50 μm. (G) Levels of CLCA1 and MUC5AC mRNA in hTECs that were transduced with lentivirus encoding CLCA1 or control shRNA. (H) For conditions in E, corresponding cellular levels of CLCA1 and MUC5AC by ELISA. All values represent mean ± SEM. *P < 0.05, increase from corresponding no IL-13 treatment control or decrease from no shRNA treatment.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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