Interferon-γ Regulation of Intestinal Epithelial Permeability

被引:83
作者
Beaurepaire, Cecile [1 ]
Smyth, David [1 ]
McKay, Derek M. [1 ]
机构
[1] Univ Calgary, Dept Physiol & Biophys, Gastrointestinal Res Grp, Calgary, AB T2N 4N1, Canada
关键词
NECROSIS-FACTOR-ALPHA; TIGHT JUNCTION PROTEINS; INFLAMMATORY-BOWEL-DISEASE; LIGHT-CHAIN KINASE; BARRIER FUNCTION; IFN-GAMMA; NITRIC-OXIDE; CROHNS-DISEASE; ION-TRANSPORT; CELL-LINE;
D O I
10.1089/jir.2008.0057
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The maintenance and regulation of the barrier function of the epithelial lining of the intestine are important homeostatic events, serving to allow selective absorption from the gut lumen while simultaneously limiting the access of bacteria into the mucosa. Interferon-gamma is a pleiotrophic cytokine produced predominantly by natural kill cells and CD4(+) T cells that under normal circumstances, and particularly during infection or inflammation, will be a component of the intestinal milieu. Use of colon-derived epithelial cell lines and, to a less extent, murine in vivo analyses, have revealed that interferon-gamma (IFN-gamma) can increase epithelial permeability as gauged by markers of paracellular permeability and bacterial transcytosis, with at least a portion of the bacteria using the transcellular permeation pathway. In this review, we describe the main characteristics of epithelial permeability and then focus on the ability of IFN-gamma to increase epithelial permeability, and the mechanism(s) thereof.
引用
收藏
页码:133 / 143
页数:11
相关论文
共 131 条
  • [1] ADAMS RB, 1993, J IMMUNOL, V150, P2356
  • [2] Claudin-2 expression induces cation-selective channels in tight junctions of epithelial cells
    Amasheh, S
    Meiri, N
    Gitter, AH
    Schöneberg, T
    Mankertz, J
    Schulzke, JD
    Fromm, M
    [J]. JOURNAL OF CELL SCIENCE, 2002, 115 (24) : 4969 - 4976
  • [3] The IFN gamma receptor: A paradigm for cytokine receptor signaling
    Bach, EA
    Aguet, M
    Schreiber, RD
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 : 563 - &
  • [4] Intestinal epithelial responses to enteric pathogens: effects on the tight junction barrier, ion transport, and inflammation
    Berkes, J
    Viswanathan, VK
    Savkovic, SD
    Hecht, G
    [J]. GUT, 2003, 52 (03) : 439 - 451
  • [5] Prolonged interferon-γ exposure decreases ion transport, NKCC1, and Na+-K+-ATPase expression in human intestinal xenografts in vivo
    Bertelsen, LS
    Eckmann, L
    Barrett, KE
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2004, 286 (01): : G157 - G165
  • [6] Cholera toxin potentiates influences of IFN-γ through activation of NF-κB and release of tumor necrosis factor-α
    Blumberg, RS
    Pitman, RS
    Taylor, CT
    Colgan, SP
    [J]. JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2005, 25 (04) : 209 - 219
  • [7] Cellular responses to interferon-gamma
    Boehm, U
    Klamp, T
    Groot, M
    Howard, JC
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 : 749 - 795
  • [8] Proinflammatory cytokines disrupt epithelial barrier function by apoptosis-independent mechanisms
    Bruewer, M
    Luegering, A
    Kucharzik, T
    Parkos, CA
    Madara, JL
    Hopkins, AM
    Nusrat, A
    [J]. JOURNAL OF IMMUNOLOGY, 2003, 171 (11) : 6164 - 6172
  • [9] Interferon-γ induces internalization of epithelial tight junction proteins via a macropinocytosis-like process
    Bruewer, M
    Utech, M
    Ivanov, AI
    Hopkins, AM
    Parkos, CA
    Nusrat, A
    [J]. FASEB JOURNAL, 2005, 19 (08) : 923 - 933
  • [10] RhoA, Rac1, and Cdc42 exert distinct effects on epithelial barrier via selective structural and biochemical modulation of junctional proteins and F-actin
    Bruewer, M
    Hopkins, AM
    Hobert, ME
    Nusrat, A
    Madara, JL
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (02): : C327 - C335