Goblet cell compound exocytosis in the defense against bacterial invasion in the colon exposed to ischemia-reperfusion

被引:36
作者
Grootjans, Joep [1 ]
Hundscheid, Inca H. [2 ]
Buurman, Wim A. [3 ]
机构
[1] Slotervaartziekenhuis, Dept Internal Med, Amsterdam, Netherlands
[2] Maastricht Univ, Med Ctr, NUTRIM Sch Nutr Toxicol & Metab, Dept Surg, Maastricht, Netherlands
[3] Maastricht Univ, Med Ctr, NUTRIM Sch Nutr Toxicol & Metab, Maastricht, Netherlands
关键词
colonic diseases; mucosal injury; intestinal barrier function; ischemia-reperfusion; mucosal barrier; GERM-FREE RAT; ENDOPLASMIC-RETICULUM; MUC2; MUCIN; COLITIS; HYPOXIA; PATTERNS; OUTCOMES;
D O I
10.4161/gmic.23866
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
In recent years, the importance of the mucus layer in the colon has become increasingly clear. Disturbance of the mucus layer has been implicated in a variety of intestinal diseases. We have recently investigated the importance of the mucus layer in colon ischemia-reperfusion (IR). Using a newly developed human and rat colon IR model, we showed that colon ischemia leads to mucus barrier breakdown. This allowed intraluminal bacteria to interact with the colonic epithelium, which was associated with an inflammatory response. Intriguingly, we found goblet cells to respond immediately by expelling their mucin granules into the gut lumen, which flushed bacteria from the colonic crypts and resulted in rapid restoration of the mucus layer during reperfusion. Our study might explain why ischemic colitis tends to have favorable outcomes and can often be treated conservatively.
引用
收藏
页码:232 / 235
页数:4
相关论文
共 36 条
[1]
[Anonymous], 2000, Gastroenterology, V118, P951
[2]
Dimerization of the human MUC2 mucin in the endoplasmic reticulum is followed by a N-glycosylation-dependent transfer of the mono- and dimers to the Golgi apparatus [J].
Asker, N ;
Axelsson, MAB ;
Olofsson, SO ;
Hansson, GC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (30) :18857-18863
[3]
O-glycosylated MUC2 monomer and dimer from LS 174T cells are water-soluble, whereas larger MUC2 species formed early during biosynthesis are insoluble and contain nonreducible intermolecular bonds [J].
Axelsson, MAB ;
Asker, N ;
Hansson, GC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (30) :18864-18870
[4]
Host-bacterial mutualism in the human intestine [J].
Bäckhed, F ;
Ley, RE ;
Sonnenburg, JL ;
Peterson, DA ;
Gordon, JI .
SCIENCE, 2005, 307 (5717) :1915-1920
[5]
Muc2 Protects against Lethal Infectious Colitis by Disassociating Pathogenic and Commensal Bacteria from the Colonic Mucosa [J].
Bergstrom, Kirk S. B. ;
Kissoon-Singh, Vanessa ;
Gibson, Deanna L. ;
Ma, Caixia ;
Montero, Marinieve ;
Sham, Ho Pan ;
Ryz, Natasha ;
Huang, Tina ;
Velcich, Anna ;
Finlay, B. Brett ;
Chadee, Kris ;
Vallance, Bruce A. .
PLOS PATHOGENS, 2010, 6 (05)
[6]
Anatomic Patterns, Patient Characteristics, and Clinical Outcomes in Ischemic Colitis: A Study of 313 Cases Supported by Histology [J].
Brandt, Lawrence J. ;
Feuerstadt, Paul ;
Blaszka, Matthew C. .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2010, 105 (10) :2245-2252
[7]
The immune system and the gut microbiota: friends or foes? [J].
Cerf-Bensussan, Nadine ;
Gaboriau-Routhiau, Valerie .
NATURE REVIEWS IMMUNOLOGY, 2010, 10 (10) :735-744
[8]
Hypoxia: an alarm signal during intestinal inflammation [J].
Colgan, Sean P. ;
Taylor, Cormac T. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2010, 7 (05) :281-287
[9]
Regulated airway goblet cell mucin secretion [J].
Davis, C. William ;
Dickey, Burton E. .
ANNUAL REVIEW OF PHYSIOLOGY, 2008, 70 :487-512
[10]
Deplancke B, 2001, AM J CLIN NUTR, V73, p1131S