CD14 is expressed and released as soluble CD14 by human intestinal epithelial cells in vitro:: Lipopolysaccharide activation of epithelial cells revisited

被引:106
作者
Funda, DP
Tucková, L
Farré, MA
Iwase, T
Moro, I
Tlaskalová-Hogenová, H
机构
[1] Acad Sci Czech Republ, Inst Microbiol, Div Immunol & Gnotobiol, CR-14220 Prague 4, Czech Republic
[2] Nihon Univ, Sch Dent, Dept Pathol, Chiyoda Ku, Tokyo 101, Japan
关键词
D O I
10.1128/IAI.69.6.3772-3781.2001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human endothelial as well as epithelial cells were shown to respond to lipopolysaccharides (LPSs). However, the expression and release of CD14 by these so-called CD14-negative cells have not been studied in detail. We investigated three human intestinal epithelial cell lines (ECLs), SW-480, HT-29, and Caco-2, for their expression of CD14 and CD11c/CD18 as well as their responsiveness to endotoxins. Fluorescence-activated cell sorter analysis revealed no expression of CD11c/CD18, but there was low expression of membrane-bound CD14 on HT-29, Caco-2, and SW-480 ECLs. Both Western blotting and reverse transcription-PCR confirmed the CD14 positivity of all three intestinal ECLs. No substantial modulation of CD14 expression was achieved after 6, 8, 18, 24, and 48 h of cultivation with 10-fold serial dilutions of LPS ranging from 0.01 ng/ml to 100 mug/ml. Interestingly, soluble CD14 was found in the tissue culture supernatants of all three ECLs. Finally, only HT-29 and SW-4801 and not Caco-21 cells; responded to LPS exposure (range, 0.01 ng/ml to 100 mug/ml) by interleukin 8 release. Thus, we show that HT-29, SW-480, and Caco-2 human intestinal ECLs express membrane-bound CD14. As Caco-2 cells did not respond to LPS, these cell lines might be an interesting model for studying the receptor complex for LPS. The fact that human intestinal epithelial cells are capable not only of expression but also of release of soluble CD14 may have important implications in vivo, e.g., in shaping the interaction between the mucosal immune system and bacteria in the gut and/or in the pathogenesis of endotoxin shock.
引用
收藏
页码:3772 / 3781
页数:10
相关论文
共 57 条
[1]   Regulatory roles for CD14 and phosphatidylinositol in the signaling via toll-like receptor 4-MD-2 [J].
Akashi, S ;
Ogata, H ;
Kirikae, F ;
Kirikae, T ;
Kawasaki, K ;
Nishijima, M ;
Shimazu, R ;
Nagai, Y ;
Fukudome, K ;
Kimoto, M ;
Miyake, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 268 (01) :172-177
[2]  
[Anonymous], MOSAIC
[3]   STRUCTURAL RELATIONSHIP BETWEEN THE SOLUBLE AND MEMBRANE-BOUND FORMS OF HUMAN MONOCYTE SURFACE GLYCOPROTEIN-CD14 [J].
BAZIL, V ;
BAUDYS, M ;
HILGERT, I ;
STEFANOVA, I ;
LOW, MG ;
ZBROZEK, J ;
HOREJSI, V .
MOLECULAR IMMUNOLOGY, 1989, 26 (07) :657-662
[4]  
BAZIL V, 1991, J IMMUNOL, V147, P1567
[5]   Lipopolysaccharide activates distinct signaling pathways in intestinal epithelial cell lines expressing toll-like receptors [J].
Cario, E ;
Rosenberg, IM ;
Brandwein, SL ;
Beck, PL ;
Reinecker, HC ;
Podolsky, DK .
JOURNAL OF IMMUNOLOGY, 2000, 164 (02) :966-972
[6]   Incorporation of leucocyte GPI-anchored proteins and protein tyrosine kinases into lipid-rich membrane domains of COS-7 cells [J].
Cebecauer, M ;
Cerny, J ;
Horejsí, V .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 243 (03) :706-710
[7]  
DENTENER MA, 1993, J IMMUNOL, V150, P2885
[8]   Inducible expression of an antibiotic peptide gene in lipopolysaccharide-challenged tracheal epithelial cells [J].
Diamond, G ;
Russell, JP ;
Bevins, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (10) :5156-5160
[9]   IMPAIRED PHAGOCYTE RESPONSES TO LIPOPOLYSACCHARIDE IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA [J].
DUCHOW, J ;
MARCHANT, A ;
CRUSIAUX, A ;
HUSSON, C ;
ALONSOVEGA, C ;
DEGROOTE, D ;
NEVE, P ;
GOLDMAN, M .
INFECTION AND IMMUNITY, 1993, 61 (10) :4280-4285
[10]   DIFFERENTIAL CYTOKINE EXPRESSION BY HUMAN INTESTINAL EPITHELIAL-CELL LINES - REGULATED EXPRESSION OF INTERLEUKIN-8 [J].
ECKMANN, L ;
JUNG, HC ;
SCHURERMALY, C ;
PANJA, A ;
MORZYCKAWROBLEWSKA, E ;
KAGNOFF, MF .
GASTROENTEROLOGY, 1993, 105 (06) :1689-1697