Studies of mucus in mouse stomach, small intestine, and colon. I. Gastrointestinal mucus layers have different properties depending on location as well as over the Peyer's patches

被引:340
作者
Ermund, Anna [1 ]
Schuette, Andre [1 ]
Johansson, Malin E. V. [1 ]
Gustafsson, Jenny K. [1 ]
Hansson, Gunnar C. [1 ]
机构
[1] Univ Gothenburg, Dept Med Biochem, S-40530 Gothenburg, Sweden
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2013年 / 305卷 / 05期
基金
瑞典研究理事会;
关键词
mucin; goblet cells; bacteria; mucus adhesiveness; mucus thickness; CYSTIC-FIBROSIS; BACTERIAL OVERGROWTH; IN-VIVO; M-CELLS; MUCIN; EPITHELIUM; MICROBIOTA; SECRETION; HOST; ACCUMULATION;
D O I
10.1152/ajpgi.00046.2013
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Colon has been shown to have a two-layered mucus system where the inner layer is devoid of bacteria. However, a complete overview of the mouse gastrointestinal mucus system is lacking. We now characterize mucus release, thickness, growth over time, adhesive properties, and penetrability to fluorescent beads from stomach to distal colon. Colon displayed spontaneous mucus release and all regions released mucus in response to carbachol and PGE(2), except the distal colon and domes of Peyer's patches. Stomach and colon had an inner mucus layer that was adherent to the epithelium. In contrast, the small intestine and Peyer's patches had a single mucus layer that was easily aspirated. The inner mucus layer of the distal colon was not penetrable to beads the size of bacteria and the inner layer of the proximal colon was only partly penetrable. In contrast, the inner mucus layer of stomach was fully penetrable, as was the small intestinal mucus. This suggests a functional organization of the intestinal mucus system, where the small intestine has loose and penetrable mucus that may allow easy penetration of nutrients, in contrast to the stomach, where the mucus provides physical protection, and the colon, where the mucus separates bacteria from the epithelium. This knowledge of the mucus system and its organization improves our understanding of the gastrointestinal tract physiology.
引用
收藏
页码:G341 / G347
页数:7
相关论文
共 31 条
[1]
Calcium and pH-dependent packing and release of the gel-forming MUC2 mucin [J].
Ambort, Daniel ;
Johansson, Malin E. V. ;
Gustafsson, Jenny K. ;
Nilsson, Harriet E. ;
Ermund, Anna ;
Johansson, Bengt R. ;
Koeck, Philip J. B. ;
Hebert, Hans ;
Hansson, Gunnar C. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (15) :5645-5650
[2]
The adherent gastrointestinal mucus gel layer: thickness and physical state in vivo [J].
Atuma, C ;
Strugala, V ;
Allen, A ;
Holm, L .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2001, 280 (05) :G922-G929
[3]
Host-bacterial mutualism in the human intestine [J].
Bäckhed, F ;
Ley, RE ;
Sonnenburg, JL ;
Peterson, DA ;
Gordon, JI .
SCIENCE, 2005, 307 (5717) :1915-1920
[4]
Paneth cell defensins: key effector molecules of innate immunity [J].
Bevins, CL .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2006, 34 :263-266
[5]
Molecular analysis of the bacterial microbiota in the human stomach [J].
Bik, EM ;
Eckburg, PB ;
Gill, SR ;
Nelson, KE ;
Purdom, EA ;
Francois, F ;
Perez-Perez, G ;
Blaser, MJ ;
Relman, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (03) :732-737
[6]
M-cells: origin, morphology and role in mucosal immunity and microbial pathogenesis [J].
Corr, Sinead C. ;
Gahan, Cormac C. G. M. ;
Hill, Colin .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2008, 52 (01) :2-12
[7]
Eradication of small intestinal bacterial overgrowth in the cystic fibrosis mouse reduces mucus accumulation [J].
De Lisle, RC ;
Roach, EA ;
Norkina, O .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2006, 42 (01) :46-52
[8]
A Delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo [J].
French, PJ ;
vanDoorninck, JH ;
Peters, RHPC ;
Verbeek, E ;
Ameen, NA ;
Marino, CR ;
deJonge, HR ;
Bijman, J ;
Scholte, BJ .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (06) :1304-1312
[9]
Bicarbonate and functional CFTR channel are required for proper mucin secretion and link cystic fibrosis with its mucus phenotype [J].
Gustafsson, Jenny K. ;
Ermund, Anna ;
Ambort, Daniel ;
Johansson, Malin E. V. ;
Nilsson, Harriet E. ;
Thorell, Kaisa ;
Hebert, Hans ;
Sjovall, Henrik ;
Hansson, Gunnar C. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2012, 209 (07) :1263-1272
[10]
Gustafsson JK, 2012, AM J PHYSIOL-GASTR L, V302, pG430, DOI [10.1152/ajpgi.00405.2011., 10.1152/ajpgi.00405.2011]