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Citations to this article

Mucus strands from submucosal glands initiate mucociliary transport of large particles
Anthony J. Fischer, … , Michael J. Welsh, Mahmoud H. Abou Alaiwa
Anthony J. Fischer, … , Michael J. Welsh, Mahmoud H. Abou Alaiwa
Published January 10, 2019
Citation Information: JCI Insight. 2019;4(1):e124863. https://doi.org/10.1172/jci.insight.124863.
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Research Article Pulmonology

Mucus strands from submucosal glands initiate mucociliary transport of large particles

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Abstract

Mucus produced by submucosal glands is a key component of respiratory mucociliary transport (MCT). When it emerges from submucosal gland ducts, mucus forms long strands on the airway surface. However, the function of those strands is uncertain. To test the hypothesis that mucus strands facilitate transport of large particles, we studied newborn pigs. In ex vivo experiments, interconnected mucus strands moved over the airway surface, attached to immobile spheres, and initiated their movement by pulling them. Stimulating submucosal gland secretion with methacholine increased the percentage of spheres that moved and shortened the delay until mucus strands began moving spheres. To disrupt mucus strands, we applied reducing agents tris-(2-carboxyethyl)phosphine and dithiothreitol. They decreased the fraction of moving spheres and delayed initiation of movement for spheres that did move. We obtained similar in vivo results with CT-based tracking of microdisks in spontaneously breathing pigs. Methacholine increased the percentage of microdisks moving and reduced the delay until they were propelled up airways. Aerosolized tris-(2-carboxyethyl)phosphine prevented those effects. Once particles started moving, reducing agents did not alter their speed either ex vivo or in vivo. These findings indicate that submucosal glands produce mucus in the form of strands and that the strands initiate movement of large particles, facilitating their removal from airways.

Authors

Anthony J. Fischer, Maria I. Pino-Argumedo, Brieanna M. Hilkin, Cullen R. Shanrock, Nicholas D. Gansemer, Anna L. Chaly, Keyan Zarei, Patrick D. Allen, Lynda S. Ostedgaard, Eric A. Hoffman, David A. Stoltz, Michael J. Welsh, Mahmoud H. Abou Alaiwa

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Total citations by year

Year: 2024 2023 2022 2021 2020 2019 2009 Total
Citations: 4 5 10 5 4 3 1 32
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Citations to this article (32)

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Pancreatic enzymes digest obstructive meconium from cystic fibrosis pig intestines
Gangadharan Nambiar G, Gonzalez Szachowicz S, Zirbes CF, Hill JJ, Powers LS, Meyerholz DK, Thornell IM, Stoltz DA, Fischer AJ
Frontiers in Pediatrics 2024
Cystic fibrosis.
Mall MA, Burgel PR, Castellani C, Davies JC, Salathe M, Taylor-Cousar JL
Nature Reviews Disease Primers 2024
Mucociliary clearance is impaired in small airways of cystic fibrosis pigs.
Stewart CG, Hilkin BM, Gansemer ND, Adam RJ, Dick DW, Sunderland JJ, Stoltz DA, Zabner J, Abou Alaiwa MH
American journal of physiology. Lung cellular and molecular physiology 2024
Artificial intelligence-guided design of lipid nanoparticles for pulmonary gene therapy.
Witten J, Raji I, Manan RS, Beyer E, Bartlett S, Tang Y, Ebadi M, Lei J, Nguyen D, Oladimeji F, Jiang AY, MacDonald E, Hu Y, Mughal H, Self A, Collins E, Yan Z, Engelhardt JF, Langer R, Anderson DG
Nature biotechnology 2024
Nebulized Menthol Impairs Mucociliary Clearance via TRPM8 and MUC5AC/MUC5B in Primary Airway Epithelial Cells.
Baumlin N, Silswal N, Dennis JS, Niloy AJ, Kim MD, Salathe M
International journal of molecular sciences 2023
Proteome of airway surface liquid and mucus in newborn wildtype and cystic fibrosis piglets.
Rodriguez-Piñeiro AM, Jaudas F, Klymiuk N, Bähr A, Hansson GC, Ermund A
Respiratory Research 2023
Autofluorescence imaging permits label-free cell type assignment and reveals the dynamic formation of airway secretory cell associated antigen passages (SAPs).
Shah VS, Hou J, Vinarsky V, Xu J, Surve MV, Lin CP, Rajagopal J
eLife 2023
Goblet cell interactions reorient bundled mucus strands for efficient airway clearance
Bos MF, Ermund A, Hansson GC, de Graaf J
2023
Tollip deficiency exaggerates airway type 2 inflammation in mice exposed to allergen and influenza A virus: role of the ATP/IL-33 signaling axis
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Frontiers in immunology 2023
Muc5b Contributes to Mucus Abnormality in Rat Models of Cystic Fibrosis
J Keith, A Henderson, C Fernandez-Petty, J Davis, A Oden, S Birket
Frontiers in physiology 2022
Elastic mucus strands impair mucociliary clearance in cystic fibrosis pigs
M Pino-Argumedo, A Fischer, B Hilkin, N Gansemer, P Allen, E Hoffman, D Stoltz, M Welsh, M Alaiwa
Proceedings of the National Academy of Sciences 2022
Tromethamine improves mucociliary clearance in cystic fibrosis pigs.
Ash JJ, Hilkin BM, Gansemer ND, Hoffman EA, Zabner J, Stoltz DA, Abou Alaiwa MH
Physiological Reports 2022
Mucins and CFTR: Their Close Relationship
Okuda K, Shaffer KM, Ehre C
International journal of molecular sciences 2022
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Hill DB, Button B, Rubinstein M, Boucher RC
Physiological reviews 2022
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Song D, Iverson E, Kaler L, Boboltz A, Scull MA, Duncan GA
Science Advances 2022
The Mucin Gene MUC5B Is Required for Normal Lung Function
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American journal of respiratory and critical care medicine 2022
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Ehre C, Hansson GC, Thornton DJ, Ostedgaard LS
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2022
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Science Advances 2022
Mucus threads from surface goblet cells clear particles from the airways
A Ermund, LN Meiss, B Dolan, F Jaudas, L Ewaldsson, A Bähr, N Klymiuk, GC Hansson
Respiratory Research 2021
Disulfide disruption reverses mucus dysfunction in allergic airway disease
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