Endothelial Fas-Ligand in Inflammatory Bowel Diseases and in Acute Appendicitis

被引:10
作者
Kokkonen, Tuomo S. [1 ,2 ,3 ]
Karttunen, Tuomo J. [2 ,3 ]
机构
[1] Lapland Hosp Dist, Rovaniemi, Finland
[2] Oulu Univ Hosp, Dept Pathol, Canc & Translat Med Res Unit, MRC Oulu, FIN-90014 Oulu, Finland
[3] Univ Oulu, FIN-90014 Oulu, Finland
关键词
Fas-ligand; Crohn's disease; ulcerative colitis; immunology; endothelium; INDUCED APOPTOSIS; EXPRESSION; VENULES; DEATH; LYMPHOCYTES; RECEPTOR; CD95L; CELLS;
D O I
10.1369/0022155415608917
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Fas-mediated induction of apoptosis is a major factor in the selection of lymphocytes and downregulation of immunological processes. In the present study, we have assessed endothelial Fas-ligand (FasL) expression in normal human ileum, appendix, and colon, and compared the expression levels with that in inflammatory bowel disease and in acute appendicitis. In a normal appendix, endothelial FasL levels were constant in almost half of the mucosal vessels; but, in the normal ileum and colon, endothelial FasL was practically restricted to areas in close proximity to lymphatic follicles, and was expressed mainly in the submucosal aspect of the follicles in the vessels with high endothelium. In samples from subjects with either Crohn's disease or ulcerative colitis, the extent of endothelial FasL expression was elevated in the submucosa and associated with an elevated number of lymphoid follicles. In inflammatory bowel disease, ulcers and areas with a high density of mononuclear cells expressing FasL also showed an elevated density of blood vessels with endothelial FasL expression. Although the function of endothelial FasL remains unclear, such a specific expression pattern suggests that endothelial FasL expression has a role in the regulation of lymphocyte access to the peripheral lymphoid tissues, including the intestinal mucosa.
引用
收藏
页码:931 / 942
页数:12
相关论文
共 38 条
[1]
The "mode" of lymphocyte extravasation through HEV of Peyer's patches and its role in normal homing and inflammation [J].
Azzali, Giacomo ;
Arcari, Maria Luisa ;
Caldara, Gaetano Felice .
MICROVASCULAR RESEARCH, 2008, 75 (02) :227-237
[2]
Cheng XL, 2010, METHOD FIND EXP CLIN, V32, P13, DOI [10.1358/inf.2010.32.1.1428742, 10.1358/mf.2010.32.1.1428742]
[3]
Oxidative stress induces the expression of Fas and Fas ligand and apoptosis in murine intestinal epithelial cells [J].
Denning, TL ;
Takaishi, H ;
Crowe, SE ;
Boldogh, I ;
Jevnikar, A ;
Ernst, PB .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (12) :1641-1650
[4]
Increased enterocyte apoptosis in inflamed areas of Crohn's disease [J].
Di Sabatino, A ;
Ciccocioppo, R ;
Luinetti, O ;
Ricevuti, L ;
Morera, R ;
Cifone, AG ;
Solcia, E ;
Corazza, GR .
DISEASES OF THE COLON & RECTUM, 2003, 46 (11) :1498-1507
[5]
Ferguson Thomas A, 2007, Chem Immunol Allergy, V92, P140, DOI 10.1159/000099265
[6]
A vision of cell death: Fas ligand and immune privilege 10 years later [J].
Ferguson, Thomas A. ;
Griffith, Thomas S. .
IMMUNOLOGICAL REVIEWS, 2006, 213 :228-238
[7]
The anatomy of mucosal immune responses [J].
Garside, P ;
Millington, O ;
Smith, KM .
ORAL TOLERANCE: NEW INSIGHTS AND PROSPECTS FOR CLINICAL APPLICATION, 2004, 1029 :9-15
[8]
HIGH ENDOTHELIAL VENULES (HEVS) - SPECIALIZED ENDOTHELIUM FOR LYMPHOCYTE MIGRATION [J].
GIRARD, JP ;
SPRINGER, TA .
IMMUNOLOGY TODAY, 1995, 16 (09) :449-457
[9]
FAS LIGAND-INDUCED APOPTOSIS AS A MECHANISM OF IMMUNE PRIVILEGE [J].
GRIFFITH, TS ;
BRUNNER, T ;
FLETCHER, SM ;
GREEN, DR ;
FERGUSON, TA .
SCIENCE, 1995, 270 (5239) :1189-1192
[10]
Hachim MY, 2006, SAUDI MED J, V27, P1815