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Peroxidase-mediated mucin cross-linking drives pathologic mucus gel formation in IL-13–stimulated airway epithelial cells
Maude A. Liegeois, Margaret Braunreuther, Annabelle R. Charbit, Wilfred W. Raymond, Monica Tang, Prescott G. Woodruff, Stephanie A. Christenson, Mario Castro, Serpil C. Erzurum, Elliot Israel, Nizar N. Jarjour, Bruce D. Levy, Wendy C. Moore, Sally E. Wenzel, Gerald G. Fuller, John V. Fahy
Maude A. Liegeois, Margaret Braunreuther, Annabelle R. Charbit, Wilfred W. Raymond, Monica Tang, Prescott G. Woodruff, Stephanie A. Christenson, Mario Castro, Serpil C. Erzurum, Elliot Israel, Nizar N. Jarjour, Bruce D. Levy, Wendy C. Moore, Sally E. Wenzel, Gerald G. Fuller, John V. Fahy
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Research Article Cell biology Pulmonology

Peroxidase-mediated mucin cross-linking drives pathologic mucus gel formation in IL-13–stimulated airway epithelial cells

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Abstract

Mucus plugs occlude airways to obstruct airflow in asthma. Studies in patients and in mouse models show that mucus plugs occur in the context of type 2 inflammation, and studies in human airway epithelial cells (HAECs) show that IL-13–activated cells generate pathologic mucus independently of immune cells. To determine how HAECs autonomously generate pathologic mucus, we used a magnetic microwire rheometer to characterize the viscoelastic properties of mucus secreted under varying conditions. We found that normal HAEC mucus exhibited viscoelastic liquid behavior and that mucus secreted by IL-13–activated HAECs exhibited solid-like behavior caused by mucin cross-linking. In addition, IL-13–activated HAECs shows increased peroxidase activity in apical secretions, and an overlaid thiolated polymer (thiomer) solution shows an increase in solid behavior that was prevented by peroxidase inhibition. Furthermore, gene expression for thyroid peroxidase (TPO), but not lactoperoxidase (LPO), was increased in IL-13–activated HAECs and both TPO and LPO catalyze the formation of oxidant acids that cross-link thiomer solutions. Finally, gene expression for TPO in airway epithelial brushings was increased in patients with asthma with high airway mucus plug scores. Together, our results show that IL-13–activated HAECs autonomously generated pathologic mucus via peroxidase-mediated cross-linking of mucin polymers.

Authors

Maude A. Liegeois, Margaret Braunreuther, Annabelle R. Charbit, Wilfred W. Raymond, Monica Tang, Prescott G. Woodruff, Stephanie A. Christenson, Mario Castro, Serpil C. Erzurum, Elliot Israel, Nizar N. Jarjour, Bruce D. Levy, Wendy C. Moore, Sally E. Wenzel, Gerald G. Fuller, John V. Fahy

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Figure 7

TPO gene expression is higher in patients with asthma, especially in patients with high airway mucus plug scores.

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TPO gene expression is higher in patients with asthma, especially in pat...
(A) Gene expression for lactoperoxidase (LPO) in airway epithelial brushings is similar in patients with asthma (n = 104) and healthy controls (n = 36). (B) Gene expression for thyroid peroxidase (TPO) in airway epithelial brushings is higher in patients with asthma than in healthy controls. Significantly different than controls, ***P < 0.001. (C) LPO gene expression does not vary greatly among patients with asthma based on airway mucus plug scores determined from quantitative analysis of their CT lung scans. P values were calculated using a Kruskal-Wallis test. Significantly different from controls, *P < 0.05. (D) TPO gene expression is highest in patients with asthma with high airway mucus plug scores. P values were calculated using a Kruskal-Wallis test. Significantly different from controls, *P < 0.05; significantly different from controls, **P < 0.01; significantly different from controls, ****P < 0.0001; significantly different from patients with asthma with a mucus plug score of zero, #P < 0.05. (E) Representative TPO immunostaining image of a tissue section from an endobronchial biopsy from a patient with asthma (n = 3 patients with asthma). Also shown is immunostaining for acetylated α-tubulin (Ac-α-Tub), which marks cilia and staining for DNA (DAPI) marking cell nuclei. The TPO immunostaining is most prominent at the apical membrane of ciliated epithelial cells. A control section shows how antigen preabsorption using human recombinant TPO (hrTPO) decrease the TPO signal intensity, providing evidence for the specificity of the TPO immunostaining signal. Scale bars: 30 μm.

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