Evidence map›Paper›PMID 39019950›Full record

ArticleScientific reports2024

Reduced sialylation of airway mucin impairs mucus transport by altering the biophysical properties of mucin.

Elex S Harris, Hannah J McIntire, Marina Mazur, Hinnerk Schulz-Hildebrandt, Hui Min Leung, Guillermo J Tearney, Stefanie Krick, Steven M Rowe, Jarrod W Barnes

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. A bidirectionalbioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Airway mucus in infection.Frontiers in physiology · 2026
    Review
  10. Article
  11. Mucosal colonization ofMicrobiology spectrum · 2025
    Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Elex S HarrisGregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, 1900 University Blvd. Tinsley Harrison Tower, Suite 422, Birmingham, AL, 35294, USA.
Hannah J McIntireGregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, 1900 University Blvd. Tinsley Harrison Tower, Suite 422, Birmingham, AL, 35294, USA.
Marina MazurGregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, 1900 University Blvd. Tinsley Harrison Tower, Suite 422, Birmingham, AL, 35294, USA.
Hinnerk Schulz-HildebrandtMassachusetts General Hospital, Boston, MA, USA.
Hui Min LeungMassachusetts General Hospital, Boston, MA, USA.
Guillermo J TearneyMassachusetts General Hospital, Boston, MA, USA.
Stefanie KrickGregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, 1900 University Blvd. Tinsley Harrison Tower, Suite 422, Birmingham, AL, 35294, USA.
Steven M Rowe *Gregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, 1900 University Blvd. Tinsley Harrison Tower, Suite 422, Birmingham, AL, 35294, USA. smrowe@uab.edu.
Jarrod W Barnes *Gregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, 1900 University Blvd. Tinsley Harrison Tower, Suite 422, Birmingham, AL, 35294, USA. jbarnes@uabmc.edu.

Funding

UAB CF Research and Translation Core CenterP30DK072482 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Brian R. Davis · 2007 to 2026
$23.0M
Translational Program in CFTR-Related Airway DiseasesR35HL135816 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ROWE, STEVEN MARK · 2017 to 2022
$6.3M
Metabolic Landscape of the Aging LungR01HL152246 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BARNES, JARROD W., THANNICKAL, VICTOR J. · 2020 to 2023
$3.2M
Training Program in Cell, Molecular, and Developmental BiologyT32GM146611 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Susan L Bellis · 2024 to 2026
$1.4M
The Role of Defective CFTR Ion Transport on Mucin Sialylation and its Consequences on Mucus PhysiologyF31HL164005 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HARRIS, ELEX S · 2022 to 2023
$60k
BLRD VA I01 BX003056Cystic Fibrosis Foundation ROWE19RONational Institutes of Health, United States P30DK072482National Institutes of Health,United States 1R35HL135816-01NHLBI NIH HHS R01 HL152246NHLBI NIH HHS R35 HL135816NIDDK NIH HHS P30 DK072482NIGMS NIH HHS T32 GM146611NIH HHS F31HL164005-02NIH HHS R01HL152246
6 · The paper itself

Abstract

Mucus stasis is a pathologic hallmark of muco-obstructive diseases, including cystic fibrosis (CF). Mucins, the principal component of mucus, are extensively modified with hydroxyl (O)-linked glycans, which are largely terminated by sialic acid. Sialic acid is a negatively charged monosaccharide and contributes to the biochemical/biophysical properties of mucins. Reports suggest that mucin sialylation may be altered in CF; however, the consequences of reduced sialylation on mucus clearance have not been fully determined. Here, we investigated the consequences of reduced sialylation on the charge state and conformation of the most prominent airway mucin, MUC5B, and defined the functional consequences of reduced sialylation on mucociliary transport (MCT). Reduced sialylation contributed to a lower charged MUC5B form and decreased polymer expansion. The inhibition of total mucin sialylation de novo impaired MCT in primary human bronchial epithelial cells and rat airways, and specific α-2,3 sialylation blockade was sufficient to recapitulate these findings. Finally, we show that ST3 beta-galactoside alpha-2,3-sialyltransferase (ST3Gal1) expression is downregulated in CF and partially restored by correcting CFTR via Elexacaftor/Tezacaftor/Ivacaftor treatment. Overall, this study demonstrates the importance of mucin sialylation in mucus clearance and identifies decreased sialylation by ST3Gal1 as a possible therapeutic target in CF and potentially other muco-obstructive diseases.

Indexed as

Mucin-5BMucusAnimalsBronchiCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorEpithelial CellsHumansMucinsMucociliary ClearanceN-Acetylneuraminic AcidRatsRespiratory MucosaSialyltransferasesCystic Fibrosis Transmembrane Conductance RegulatorMUC5B protein, humanMucin-5BMucinsN-Acetylneuraminic AcidSialyltransferases

Identifiers

PMID39019950
PMCPMC11255327

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.