Migration of human intestinal lamina propria lymphocytes, macrophages and eosinophils following the loss of surface epithelial cells

被引:72
作者
Mahida, YR
Galvin, AM
Gray, T
Makh, S
McAlindon, ME
Sewell, HF
Podolsky, DK
机构
[1] UNIV NOTTINGHAM HOSP,QUEENS MED CTR,DIV IMMUNOL,NOTTINGHAM NG7 2UH,ENGLAND
[2] UNIV NOTTINGHAM HOSP,QUEENS MED CTR,DIV PATHOL,NOTTINGHAM NG7 2UH,ENGLAND
[3] UNIV NOTTINGHAM HOSP,QUEENS MED CTR,INST INFECT & IMMUN,NOTTINGHAM NG7 2UH,ENGLAND
[4] HARVARD UNIV,SCH MED,BOSTON,MA
[5] MASSACHUSETTS GEN HOSP,GASTROINTESTINAL UNIT,BOSTON,MA 02114
关键词
basement membrane; lymphocytes; macrophages; eosinophils; intestine;
D O I
10.1046/j.1365-2249.1997.4481346.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lymphocytes and macrophages are present in the normal intestinal lamina propria, separated from the epithelial monolayer by the basement membrane. There is evidence for movement of mononuclear cells through the lamina propria, entering from the systemic circulation and exiting via lymphatic channels. The goal of our studies was to investigate the capacity of cells to migrate out from the lamina propria into the lumen following the loss of surface epithelial cells. An in vitro model was therefore established in which normal human intestinal mucosal samples, denuded of the surface epithelium, were maintained in culture. Electron microscopy showed that during culture, large numbers (> 2 x 10(6)/g tissue per 24 h) of cells migrated out of the lamina propria via discrete 'tunnels' which were in continuity with pores (diameter <4 mu m) in the basement membrane. The emigrating cells were T cells (68.5 +/- 5.1%), macrophages (10.5 +/- 1.3%) and eosinophils (7.1 +/- 1.3%). Our studies have therefore demonstrated, for the first time, the capacity for large numbers of lymphocytes, macrophages and eosinophils to migrate out of the lamina propria, via basement membrane pores. We postulate that such emigration of cells occurs in vivo following the loss of surface epithelial cells due to injury, and could represent an important form of host defence against luminal microorganisms and also facilitate wound repair by enhancing restitution by neighbouring epithelial cells, via peptide factors.
引用
收藏
页码:377 / 386
页数:10
相关论文
共 37 条
[1]   PHAGOCYTES IN CELL-SUSPENSIONS OF HUMAN-COLON MUCOSA [J].
BEEKEN, W ;
NORTHWOOD, I ;
BELIVEAU, C ;
GUMP, D .
GUT, 1987, 28 (08) :976-980
[2]   ALPHA-4-BETA-7-INTEGRIN MEDIATES LYMPHOCYTE BINDING TO THE MUCOSAL VASCULAR ADDRESSIN MADCAM-1 [J].
BERLIN, C ;
BERG, EL ;
BRISKIN, MJ ;
ANDREW, DP ;
KILSHAW, PJ ;
HOLZMANN, B ;
WEISSMAN, IL ;
HAMANN, A ;
BUTCHER, EC .
CELL, 1993, 74 (01) :185-195
[3]   IMMUNOBIOLOGY AND IMMUNOPATHOLOGY OF HUMAN GUT MUCOSA - HUMORAL IMMUNITY AND INTRAEPITHELIAL LYMPHOCYTES [J].
BRANDTZAEG, P ;
HALSTENSEN, TS ;
KETT, K ;
KRAJCI, P ;
KVALE, D ;
ROGNUM, TO ;
SCOTT, H ;
SOLLID, LM .
GASTROENTEROLOGY, 1989, 97 (06) :1562-1584
[4]   ISOLATION AND FUNCTIONAL CHARACTERIZATION OF HUMAN INTESTINAL MUCOSAL LYMPHOID-CELLS [J].
BULL, DM ;
BOOKMAN, MA .
JOURNAL OF CLINICAL INVESTIGATION, 1977, 59 (05) :966-974
[5]   FUNCTIONAL INTERLEUKIN-2 RECEPTORS ON INTESTINAL EPITHELIAL-CELLS [J].
CIACCI, C ;
MAHIDA, YR ;
DIGNASS, A ;
KOIZUMI, M ;
PODOLSKY, DK .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (01) :527-532
[6]   TRANSFORMING GROWTH-FACTOR-BETA REGULATION OF MIGRATION IN WOUNDED RAT INTESTINAL EPITHELIAL MONOLAYERS [J].
CIACCI, C ;
LIND, SE ;
PODOLSKY, DK .
GASTROENTEROLOGY, 1993, 105 (01) :93-101
[7]   CYTOKINE MODULATION OF INTESTINAL EPITHELIAL-CELL RESTITUTION - CENTRAL ROLE OF TRANSFORMING GROWTH-FACTOR-BETA [J].
DIGNASS, AU ;
PODOLSKY, DK .
GASTROENTEROLOGY, 1993, 105 (05) :1323-1332
[8]   FIBROBLAST GROWTH-FACTORS MODULATE INTESTINAL EPITHELIAL-CELL GROWTH AND MIGRATION [J].
DIGNASS, AU ;
TSUNEKAWA, S ;
PODOLSKY, DK .
GASTROENTEROLOGY, 1994, 106 (05) :1254-1262
[9]   GUT MUCOSAL LYMPHOCYTES IN INFLAMMATORY BOWEL-DISEASE - ISOLATION AND PRELIMINARY FUNCTIONAL-CHARACTERIZATION [J].
FIOCCHI, C ;
BATTISTO, JR ;
FARMER, RG .
DIGESTIVE DISEASES AND SCIENCES, 1979, 24 (09) :705-717
[10]  
HEATLEY RV, 1982, GASTROENTEROLOGY, V82, P268