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Mucus

Anatomy and Physiology · NLM MeSH · updated 2026-10-31 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 5 min read

The viscous secretion of mucous membranes.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (905 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

The viscous secretion of mucous membranes. It contains mucin, white blood cells, water, inorganic salts, and exfoliated cells.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Where it fits in the MeSH classification

Broader topics
Bodily Secretions
Narrower topics
Cervix Mucus
See also
Drainage, Postural

Research landscape

PubMed indexes 14,591 records tagged with the MeSH heading “Mucus” (counts retrieved 2026-10-31). 1,842 of them (12.6%) were published from 2020 onward, and the busiest period so far is through 1999 with 8,404 records.

Reviews account for 1,457 records (10.0%) and meta-analyses for 30. Randomized controlled trials number 216 (1.5%) as a share of all records on the topic. Randomized trials make up only a small share of this literature, so much of what is known comes from laboratory, observational or descriptive work.

PubMed records by publication periodthrough 1999: 8,404 records; 2000-2009: 1,829 records; 2010-2019: 2,516 records; 2020 onward: 1,842 records8,404through 19991,8292000-20092,5162010-20191,8422020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 19998,404
2000-20091,829
2010-20192,516
2020 onward1,842
Share of records by publication typeReviews: 10.0 percent; Meta-analyses: 0.2 percent; Randomized controlled trials: 1.5 percentReviews10.0% (1,457)Meta-analyses0.2% (30)Randomized controlled trials1.5% (216)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 14,591 PubMed records
TypeRecordsShare
Reviews1,45710.0%
Meta-analyses300.2%
Randomized controlled trials2161.5%

Method: PubMed query "Mucus"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-31.

Reading the evidence in anatomy and physiology

Anatomy describes how body structures are built and physiology describes how they normally work, so most findings here are descriptive or mechanistic rather than evidence about treatment. Much of what is known comes from dissection, imaging, tissue studies and experiments in animals, and measurements in healthy volunteers can differ from those in people with disease or at different ages. Normal ranges vary between individuals and populations. Check whether a result was measured in people or in another species, the age and health of the participants, and the method used.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Slimy partners: the mucus barrier and gut microbiome in ulcerative colitis
Fang J, Wang H, Zhou Y, Zhang H, Zhou H, Zhang X
2021Review article
Design not recorded in structured metadata
193cc by
PMID 34002011 · DOI · PMC8178360
Development and Functional Properties of Intestinal Mucus Layer in Poultry
Duangnumsawang Y, Zentek J, Goodarzi Boroojeni F
2021Review article
Design not recorded in structured metadata
122cc by
PMID 34671361 · DOI · PMC8521165
The Cervicovaginal Mucus Barrier
Lacroix G, Gouyer V, Gottrand F, Desseyn JL
2020Review article
Design not recorded in structured metadata
119cc by
PMID 33158227 · DOI · PMC7663572
Akkermansia muciniphila modulates intestinal mucus composition to counteract high-fat diet-induced obesity in mice
Paone P, Petitfils C, Puel A, Latousakis D, de Vos WM, Delzenne NM, et al.
2026Research article
Design not recorded in structured metadata
10cc by
PMID 41511159 · DOI · PMC12795273

Slimy partners: the mucus barrier and gut microbiome in ulcerative colitis [1]

Review article Fang J, Wang H, Zhou Y, Zhang H, Zhou H, Zhang X · · 2021 · cited 193 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Ulcerative colitis (UC) is a chronic recurrent intestinal inflammatory disease characterized by high incidence and young onset age.
Closing excerpt
Our review mainly focuses on the complicated communication between the mucus barrier and gut microbiome to explore a promising new avenue for UC therapy.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (142 words)

Ulcerative colitis (UC) is a chronic recurrent intestinal inflammatory disease characterized by high incidence and young onset age. Recently, there have been some interesting findings in the pathogenesis of UC. The mucus barrier, which is composed of a mucin complex rich in O-glycosylation, not only provides nutrients and habitat for intestinal microbes but also orchestrates the taming of germs. In turn, the gut microbiota modulates the production and secretion of mucins and stratification of the mucus layers. Active bidirectional communication between the microbiota and its 'slimy' partner, the mucus barrier, seems to be a continually performed concerto, maintaining homeostasis of the gut ecological microenvironment. Any abnormalities may induce a disorder in the gut community, thereby causing inflammatory damage. Our review mainly focuses on the complicated communication between the mucus barrier and gut microbiome to explore a promising new avenue for UC therapy.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 34002011 · DOI · PMC8178360

Development and Functional Properties of Intestinal Mucus Layer in Poultry [2]

Review article Duangnumsawang Y, Zentek J, Goodarzi Boroojeni F · · 2021 · cited 122 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Intestinal mucus plays important roles in protecting the epithelial surfaces against pathogens, supporting the colonization with commensal bacteria, maintaining an appropriate environment for digestion, as well as facilitating nutrient transport from the lumen to the underlying epithelium.
Closing excerpt
Given the significance of this loss and the lack of precise data, this matter needs to be carefully investigated in the future and the nutritional strategies reducing this loss have to be defined better.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (347 words)

Intestinal mucus plays important roles in protecting the epithelial surfaces against pathogens, supporting the colonization with commensal bacteria, maintaining an appropriate environment for digestion, as well as facilitating nutrient transport from the lumen to the underlying epithelium. The mucus layer in the poultry gut is produced and preserved by mucin-secreting goblet cells that rapidly develop and mature after hatch as a response to external stimuli including environmental factors, intestinal microbiota as well as dietary factors. The ontogenetic development of goblet cells affects the mucin composition and secretion, causing an alteration in the physicochemical properties of the mucus layer. The intestinal mucus prevents the invasion of pathogens to the epithelium by its antibacterial properties (e.g. β-defensin, lysozyme, avidin and IgA) and creates a physical barrier with the ability to protect the epithelium from pathogens. Mucosal barrier is the first line of innate defense in the gastrointestinal tract. This barrier has a selective permeability that allows small particles and nutrients passing through. The structural components and functional properties of mucins have been reviewed extensively in humans and rodents, but it seems to be neglected in poultry. This review discusses the impact of age on development of goblet cells and their mucus production with relevance for the functional characteristics of mucus layer and its protective mechanism in the chicken's intestine. Dietary factors directly and indirectly (through modification of the gut bacteria and their metabolic activities) affect goblet cell proliferation and differentiation and can be used to manipulate mucosal integrity and dynamic. However, the mode of action and mechanisms behind these effects need to be studied further. As mucins resist to digestion processes, the sloughed mucins can be utilized by bacteria in the lower part of the gut and are considered as endogenous loss of protein and energy to animal. Hydrothermal processing of poultry feed may reduce this loss by reduction in mucus shedding into the lumen. Given the significance of this loss and the lack of precise data, this matter needs to be carefully investigated in the future and the nutritional strategies reducing this loss have to be defined better.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 34671361 · DOI · PMC8521165

The Cervicovaginal Mucus Barrier [3]

Review article Lacroix G, Gouyer V, Gottrand F, Desseyn JL · · 2020 · cited 119 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Preterm births are a global health priority that affects 15 million babies every year worldwide.
Closing excerpt
We also review the current state of knowledge of gel-forming mucins contained in mouse cervicovaginal mucus and the mouse models used to study bacterial vaginosis.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (181 words)

Preterm births are a global health priority that affects 15 million babies every year worldwide. There are no effective prognostic and therapeutic strategies relating to preterm delivery, but uterine infections appear to be a major cause. The vaginal epithelium is covered by the cervicovaginal mucus, which is essential to health because of its direct involvement in reproduction and functions as a selective barrier by sheltering the beneficial lactobacilli while helping to clear pathogens. During pregnancy, the cervical canal is sealed with a cervical mucus plug that prevents the vaginal flora from ascending toward the uterine compartment, which protects the fetus from pathogens. Abnormalities of the cervical mucus plug and bacterial vaginosis are associated with a higher risk of preterm delivery. This review addresses the current understanding of the cervicovaginal mucus and the cervical mucus plug and their interactions with the microbial communities in both the physiological state and bacterial vaginosis, with a focus on gel-forming mucins. We also review the current state of knowledge of gel-forming mucins contained in mouse cervicovaginal mucus and the mouse models used to study bacterial vaginosis.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 33158227 · DOI · PMC7663572

Akkermansia muciniphila modulates intestinal mucus composition to counteract high-fat diet-induced obesity in mice [4]

Research article Paone P, Petitfils C, Puel A, Latousakis D, de Vos WM, Delzenne NM, et al. · · 2026 · cited 10 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
ObjectiveThis study investigates whether live Akkermansia muciniphila MucT supplementation can counteract obesity and metabolic dysfunctions induced by a high-fat diet (HFD) by modulating intestinal mucus production, secretion and composition.
Closing excerpt
This reinforces its potential as a therapeutic strategy for metabolic disorders associated with gut microbiota alterations.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (235 words)

ObjectiveThis study investigates whether live Akkermansia muciniphila MucT supplementation can counteract obesity and metabolic dysfunctions induced by a high-fat diet (HFD) by modulating intestinal mucus production, secretion and composition.DesignC57BL/6J mice were fed an HFD with or without live A. muciniphila MucT (2 × 108 CFU per day) supplementation or a control diet for 6 weeks. Body weight, fat mass gain and metabolic markers were measured. Intestinal mucus characteristics were assessed via gene expression analysis of mucins and analysed mucin glycosylation by tandem mass spectrometry (MS/MS).ResultsMice receiving live A. muciniphila MucT exhibited reduced body weight gain and fat mass accumulation compared to HFD controls, without changes in muscle mass. A. muciniphila improved gut barrier integrity by increasing antimicrobial peptide expression in the jejunum and in the colon of HFD-fed mice. Furthermore, live A. muciniphila MucT influenced markers of goblet cell differentiation and restored the expression of mucin markers altered by HFD. Specifically, live A. muciniphila MucT counteracted HFD-induced mucin 3 (Muc3) expression depletion in the colon. Although the overall mucus thickness was not affected by live A. muciniphila MucT, the bacteria significantly modulated mucin glycans composition. Live A. muciniphila MucT did not change the gut microbiota composition.ConclusionThese findings highlight the protective effects of live A. muciniphila MucT against diet-induced metabolic dysfunctions by modulating adiposity, mucus layer composition, and glycan profiles. This reinforces its potential as a therapeutic strategy for metabolic disorders associated with gut microbiota alterations.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 41511159 · DOI · PMC12795273

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Airway mucus function and dysfunction [5]
    Fahy JV, Dickey BF · N Engl J Med · 2010 · cited 1,302 times (Europe PMC)
  • Research article Mucus-penetrating nanoparticles for drug and gene delivery to mucosal tissues [6]
    Lai SK, Wang YY, Hanes J · Adv Drug Deliv Rev · 2009 · cited 1,282 times (Europe PMC)
  • Research article Mucus barrier, mucins and gut microbiota: the expected slimy partners? [7]
    Paone P, Cani PD · Gut · 2020 · cited 1,267 times (Europe PMC)
  • Research article The gastrointestinal mucus system in health and disease [8]
    Johansson ME, Sjövall H, Hansson GC · Nat Rev Gastroenterol Hepatol · 2013 · cited 1,102 times (Europe PMC)
  • Research article The mucus and mucins of the goblet cells and enterocytes provide the first defense line of the gastrointestinal tract and interact with the immune system [9]
    Pelaseyed T, Bergström JH, Gustafsson JK, Ermund A, Birchenough GM, Schütte A, et al. · Immunol Rev · 2014 · cited 992 times (Europe PMC)
  • Research article Barrier properties of mucus [10]
    Cone RA · Adv Drug Deliv Rev · 2009 · cited 990 times (Europe PMC)

References

  1. Fang J, Wang H, Zhou Y, Zhang H, Zhou H, Zhang X. Slimy partners: the mucus barrier and gut microbiome in ulcerative colitis. . 2021. PMID 34002011 · DOI · PMC8178360
  2. Duangnumsawang Y, Zentek J, Goodarzi Boroojeni F. Development and Functional Properties of Intestinal Mucus Layer in Poultry. . 2021. PMID 34671361 · DOI · PMC8521165
  3. Lacroix G, Gouyer V, Gottrand F, Desseyn JL. The Cervicovaginal Mucus Barrier. . 2020. PMID 33158227 · DOI · PMC7663572
  4. Paone P, Petitfils C, Puel A, Latousakis D, de Vos WM, Delzenne NM, et al.. Akkermansia muciniphila modulates intestinal mucus composition to counteract high-fat diet-induced obesity in mice. . 2026. PMID 41511159 · DOI · PMC12795273
  5. Fahy JV, Dickey BF. Airway mucus function and dysfunction. N Engl J Med. 2010. PMID 21121836 · DOI · PMC4048736
  6. Lai SK, Wang YY, Hanes J. Mucus-penetrating nanoparticles for drug and gene delivery to mucosal tissues. Adv Drug Deliv Rev. 2009. PMID 19133304 · DOI · PMC2667119
  7. Paone P, Cani PD. Mucus barrier, mucins and gut microbiota: the expected slimy partners?. Gut. 2020. PMID 32917747 · DOI · PMC7677487
  8. Johansson ME, Sjövall H, Hansson GC. The gastrointestinal mucus system in health and disease. Nat Rev Gastroenterol Hepatol. 2013. PMID 23478383 · DOI · PMC3758667
  9. Pelaseyed T, Bergström JH, Gustafsson JK, Ermund A, Birchenough GM, Schütte A, et al.. The mucus and mucins of the goblet cells and enterocytes provide the first defense line of the gastrointestinal tract and interact with the immune system. Immunol Rev. 2014. PMID 24942678 · DOI · PMC4281373
  10. Cone RA. Barrier properties of mucus. Adv Drug Deliv Rev. 2009. PMID 19135107 · DOI

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-10-31.

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At a glance

14,591
PubMed records on this heading
13%
published since 2020
1,457
review articles
216
randomized trials
10
verified references below

Counts come from PubMed on 2026-10-31; they show how much has been written, not how strong the evidence is.

Related topics See all →

  • SputumAnatomy and Physiology
  • Mucociliary ClearanceAnatomy and Physiology
  • Goblet CellsAnatomy and Physiology
  • Gastric JuiceAnatomy and Physiology
  • Gastric MucosaAnatomy and Physiology

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