Indigenous microbes and their soluble factors differentially modulate intestinal glycosylation steps in vivo - Use of a "lectin assay'' to survey in vivo glycosylation changes

被引:37
作者
Freitas, M
Axelsson, LG
Cayuela, C
Midtvedt, T
Trugnan, G
机构
[1] Univ Paris 06, CHU St Antoine, INSERM, UMR 538, F-75012 Paris, France
[2] Danone Vitapole, Nutrivaleur Dept, F-91767 Palaiseau, France
[3] Karolinska Hosp, Dept Gastroenterol & Hepatol, S-10401 Stockholm, Sweden
[4] Karolinska Inst, Lab Med Microbial Ecol, Dept Cellular & Mol Biol, S-17177 Stockholm, Sweden
关键词
host-microbial cross-talk; intestinal cells; glycosylation; gnotobiotic mice; B; thetaiotaomicron;
D O I
10.1007/s00418-005-0004-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It has been shown that Bacteroides thetaiotaomicron, a representative member of the gut microflora, signals intestinal epithelial cells both in vivo and in vitro and modulate specific glycosylation processes that may mediate intestinal functions. However it is not known whether these modulations depend on the presence of live bacteria or may be elicited by soluble factors produced in vitro by this bacterium. We used lectins and an histochemical approach to survey tissue sections prepared from various cellular compartments of the small and large intestine of NRMI/KI mice grown under gnotobiotic conditions. We compared the results obtained with bacterial culture supernatant and live B. thetaiotaomicron to those obtained from germ-free mice or mice having a conventional microflora. This approach allowed us to conclude that (1) a small but specific number of glycan patterns were restored after treatment with bacterial culture supernatant and (2) the B. thetaiotaomicron associated mice restored a larger number of patterns, however, the complete conventional mice pattern must be a function of the whole microflora in the gut. The possibility to modulate this complex glycosylation pattern by introducing exogenous bacteria and bacterial products should be considered as a promising approach towards understanding the molecular basis of microbial-host interactions.
引用
收藏
页码:423 / 433
页数:11
相关论文
共 27 条
[1]  
Banasaz M., 2001, Microbial Ecology in Health and Disease, V13, P135
[2]  
BREIMER ME, 1982, J BIOL CHEM, V257, P557
[3]   A model of host-microbial interactions in an open mammalian ecosystem [J].
Bry, L ;
Falk, PG ;
Midtvedt, T ;
Gordon, JI .
SCIENCE, 1996, 273 (5280) :1380-1383
[4]   Role of oligosaccharides and glycoconjugates in intestinal host defense [J].
Dai, DW ;
Nanthkumar, NN ;
Newburg, DS ;
Walker, WA .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2000, 30 :S23-S33
[5]   LECTINS ARE SENSITIVE TOOLS FOR DEFINING THE DIFFERENTIATION PROGRAMS OF MOUSE GUT EPITHELIAL-CELL LINEAGES [J].
FALK, P ;
ROTH, KA ;
GORDON, JI .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (06) :G987-G1003
[6]   Creating and maintaining the gastrointestinal ecosystem: What we know and need to know from gnotobiology [J].
Falk, PG ;
Hooper, LV ;
Midtvedt, T ;
Gordon, JI .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1998, 62 (04) :1157-+
[7]   Host-pathogens cross-talk. Indigenous bacteria and probiotics also play the game [J].
Freitas, M ;
Tavan, E ;
Cayuela, C ;
Diop, L ;
Sapin, C ;
Trugnan, G .
BIOLOGY OF THE CELL, 2003, 95 (08) :503-506
[8]   Microbial-host interactions specifically control the glycosylation pattern in intestinal mouse mucosa [J].
Freitas, M ;
Axelsson, LG ;
Cayuela, C ;
Midtvedt, T ;
Trugnan, G .
HISTOCHEMISTRY AND CELL BIOLOGY, 2002, 118 (02) :149-161
[9]  
FREITAS M, 2000, MICROB ECOL HLTH D S, V2, P165
[10]   A heat labile soluble factor from Bacteroides thetaiotaomicron VPI-5482 specifically increases the galactosylation pattern of HT29-MTX cells [J].
Freitas, W ;
Cayuela, C ;
Antoine, JM ;
Piller, F ;
Sapin, C ;
Trugnan, G .
CELLULAR MICROBIOLOGY, 2001, 3 (05) :289-300