The role of mast cells in functional GI disorders

被引:277
|
作者
Wouters, Mira M. [1 ]
Vicario, Maria [2 ,3 ,4 ]
Santos, Javier [2 ,3 ,4 ]
机构
[1] Univ Hosp Leuven, Translat Res Ctr Gastrointestinal Disorders TARGI, Leuven, Belgium
[2] Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Gastroenterol,Vall dHebron Inst Recerca, Neuroimmuno Gastroenterol Lab,Digest Dis Res Unit, E-08193 Barcelona, Spain
[3] Univ Autonoma Barcelona, Fac Med, E-08193 Barcelona, Spain
[4] Ctr Invest Biomed Red Enfermedades Hepat & Digest, Barcelona, Spain
关键词
IRRITABLE-BOWEL-SYNDROME; ORAL SODIUM CROMOGLYCATE; MUCOSAL IMMUNE-SYSTEM; VISCERAL HYPERSENSITIVITY; ABDOMINAL-PAIN; INTESTINAL PERMEABILITY; ULCERATIVE-COLITIS; BARRIER FUNCTION; MACROMOLECULAR PERMEABILITY; GASTROINTESTINAL SYMPTOMS;
D O I
10.1136/gutjnl-2015-309151
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Functional gastrointestinal disorders (FGIDs) are characterized by chronic complaints arising from disorganized brain-gut interactions leading to dysmotility and hypersensitivity. The two most prevalent FGIDs, affecting up to 16-26% of worldwide population, are functional dyspepsia and irritable bowel syndrome. Their etiopathogenic mechanisms remain unclear, however, recent observations reveal low-grade mucosal inflammation and immune activation, in association with impaired epithelial barrier function and aberrant neuronal sensitivity. These findings come to challenge the traditional view of FGIDs as pure functional disorders, and relate the origin to a tangible organic substrate. The mucosal inflammatory infiltrate is dominated by mast cells, eosinophils and intraepithelial lymphocytes in the intestine of FGIDs. It is well established that mast cell activation can generate epithelial and neuro-muscular dysfunction and promote visceral hypersensitivity and altered motility patterns in FGIDs, postoperative ileus, food allergy and inflammatory bowel disease. This review will discuss the role of mucosal mast cells in the gastrointestinal tract with a specific focus on recent advances in disease mechanisms and clinical management in irritable bowel syndrome and functional dyspepsia.
引用
收藏
页码:155 / 168
页数:14
相关论文
共 50 条
  • [1] Mastocytic Enterocolits and the Role of Mast Cells in Functional and Inflammatory Intestinal Disorders: A Systematic Review
    Capannolo, Annalisa
    Ciccone, Fabiana
    Latella, Giovanni
    DIGESTIVE DISEASES, 2018, 36 (06) : 409 - 416
  • [2] Functional gastrointestinal disorders and mast cells: implications for therapy
    Barbara, G
    Stanghellini, V
    De Giorgio, R
    Corinaldesi, R
    NEUROGASTROENTEROLOGY AND MOTILITY, 2006, 18 (01) : 6 - 17
  • [3] The role of bile acids in functional GI disorders
    Appleby, Richard N.
    Walters, Julian R. F.
    NEUROGASTROENTEROLOGY AND MOTILITY, 2014, 26 (08) : 1057 - 1069
  • [4] Mucosal permeability and mast cells as targets for functional gastrointestinal disorders
    Keita, Asa V.
    Soderholm, Johan D.
    CURRENT OPINION IN PHARMACOLOGY, 2018, 43 : 66 - 71
  • [5] The Role of Mast Cells in Irritable Bowel Syndrome
    Lee, Kang Nyeong
    Lee, Oh Young
    GASTROENTEROLOGY RESEARCH AND PRACTICE, 2016, 2016
  • [6] Role of microbiota in the pathogenesis of functional disorders of the lower GI tract: Work in progress
    Jalanka, Jonna
    Spiller, Robin
    NEUROGASTROENTEROLOGY AND MOTILITY, 2017, 29 (10) : 1 - 5
  • [7] Mast cells in gastrointestinal disorders
    Bischoff, Stephan C.
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2016, 778 : 139 - 145
  • [8] Central Neuromodulators for Treating Functional GI Disorders: A Primer
    Sobin, W. Harley
    Heinrich, Thomas W.
    Drossman, Douglas A.
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2017, 112 (05) : 693 - 702
  • [9] The role of eosinophils and mast cells in intestinal functional disease
    Walker M.M.
    Warwick A.
    Ung C.
    Talley N.J.
    Current Gastroenterology Reports, 2011, 13 (4) : 323 - 330
  • [10] Ion channelopathies in functional GI disorders
    Beyder, Arthur
    Farrugia, Gianrico
    AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2016, 311 (04): : G581 - G586