VAMP8-mediated MUC2 mucin exocytosis from colonic goblet cells maintains innate intestinal homeostasis

被引:89
作者
Cornick, Steve [1 ]
Kumar, Manish [1 ]
Moreau, France [1 ]
Gaisano, Herbert [2 ,3 ]
Chadee, Kris [1 ]
机构
[1] Univ Calgary, Snyder Inst Chron Dis, Dept Microbiol Immunol & Infect Dis, Calgary, AB, Canada
[2] Univ Toronto, Dept Med, Toronto, ON, Canada
[3] Univ Toronto, Dept Physiol, Toronto, ON, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ENDOPLASMIC-RETICULUM STRESS; ENTAMOEBA-HISTOLYTICA; MICROBIAL COMMUNITIES; LYMPHOID-CELLS; STEM-CELLS; IN-VITRO; TGF-BETA; INFLAMMATION; BARRIER; SECRETION;
D O I
10.1038/s41467-019-11811-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The mucus layer is the first line of innate host defense in the gut that protects the epithelium by spatially separating commensal bacteria. MUC2 mucin is produced and stored by goblet cells that is constitutively exocytosed or hyper secreted upon sensing a threat. How coordinated mucus exocytosis maintains homeostasis in the intestinal epithelium and modulates the immunological landscape remains elusive. Here we describe how the vesicle SNARE protein VAMP8 coordinates mucin exocytosis from goblet cells. Vamp8(-/-) exhibit a mild pro-inflammatory state basally due to an altered mucus layer and increased encounters with microbial antigens. Microbial diversity shifts to a detrimental microbiota with an increase abundance of pathogenic and mucolytic bacteria. To alleviate the heavy microbial burden and inflammatory state basally, Vamp8(-/-) skews towards tolerance. Despite this, Vamp8(-/-) is highly susceptible to both chemical and infectious colitis demonstrating the fragility of the intestinal mucosa without proper mucus exocytosis mechanisms.
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页数:14
相关论文
共 53 条
[1]
Nod2: The intestinal gate keeper [J].
Al Nabhani, Ziad ;
Dietrich, Gilles ;
Hugot, Jean-Pierre ;
Barreau, Frederick .
PLOS PATHOGENS, 2017, 13 (03)
[2]
Increased susceptibility to colitis and colorectal tumors in mice lacking core 3-derived O-glycans [J].
An, Guangyu ;
Wei, Bo ;
Xia, Baoyun ;
McDaniel, J. Michael ;
Ju, Tongzhong ;
Cummings, Richard D. ;
Braun, Jonathan ;
Xia, Lijun .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (06) :1417-1429
[3]
[Anonymous], 2011, TOXINS
[4]
Generation of Multimillion-Sequence 16S rRNA Gene Libraries from Complex Microbial Communities by Assembling Paired-End Illumina Reads [J].
Bartram, Andrea K. ;
Lynch, Michael D. J. ;
Stearns, Jennifer C. ;
Moreno-Hagelsieb, Gabriel ;
Neufeld, Josh D. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2011, 77 (11) :3846-3852
[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]
INNATE IMMUNITY A sentinel goblet cell guards the colonic crypt by triggering Nlrp6-dependent Muc2 secretion [J].
Birchenough, George M. H. ;
Nystrom, Elisabeth E. L. ;
Johansson, Malin E. V. ;
Hansson, Gunnar C. .
SCIENCE, 2016, 352 (6293) :1535-1542
[7]
MUCIN AND NONMUCIN SECRETAGOGUE ACTIVITY OF ENTAMOEBA-HISTOLYTICA AND CHOLERA-TOXIN IN RAT COLON [J].
CHADEE, K ;
KELLER, K ;
FORSTNER, J ;
INNES, DJ ;
RAVDIN, JI .
GASTROENTEROLOGY, 1991, 100 (04) :986-997
[8]
A Functional Role for Nlrp6 in Intestinal Inflammation and Tumorigenesis [J].
Chen, Grace Y. ;
Liu, Maochang ;
Wang, Fuyuan ;
Bertin, John ;
Nunez, Gabriel .
JOURNAL OF IMMUNOLOGY, 2011, 186 (12) :7187-7194
[9]
Cornick S, 2017, MBIO, V8, DOI [10.1128/mbio.01323-17, 10.1128/mBio.01323-17]
[10]
Cornick S, 2017, TISSUE BARRIERS, V5, DOI 10.1080/21688370.2017.1283386