A Caenorhabditis elegans Glycolipid-binding Galectin Functions in Host Defense against Bacterial Infection

被引:50
作者
Ideo, Hiroko
Fukushima, Keiko
Gengyo-Ando, Keiko [2 ,3 ]
Mitani, Shohei [2 ,3 ]
Dejima, Katsufumi [4 ]
Nomura, Kazuya [2 ,4 ]
Yamashita, Katsuko [1 ,2 ]
机构
[1] Tokyo Inst Technol, Innovat Res Initiat, Midori Ku, Yokohama, Kanagawa 2268503, Japan
[2] Core Res Evolut Sci & Technol, Saitama 3320012, Japan
[3] Tokyo Womens Med Univ, Sch Med, Dept Physiol, Tokyo 1628666, Japan
[4] Kyushu Univ, Fac Sci 33, Dept Biol, Fukuoka 8128581, Japan
关键词
BACILLUS-THURINGIENSIS; MEMBRANE MICRODOMAINS; SPECIFICITY; MUTANTS; PROTEIN; GLYCOSPHINGOLIPIDS; EXPRESSION; SULFATIDES; NEMATODES; DOMAINS;
D O I
10.1074/jbc.M109.038257
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
Galectins are a family of beta-galactoside-binding proteins that are widely found among animal species and that regulate diverse biological phenomena. To study the biological function of glycolipid-binding galectins, we purified recombinant Caenorhabditis elegans galectins (LEC-1-11) and studied their binding to C. elegans glycolipids. We found that LEC-8 binds to glycolipids in C. elegans through carbohydrate recognition. It has been reported that Cry5B-producing Bacillus thuringiensis strains can infect C. elegans and that the C. elegans Cry5B receptor molecules are glycolipids. We found that Cry5B and LEC-8 bound to C. elegans glycolipid-coated plates in a dose-dependent manner and that Cry5B binding to glycolipids was inhibited by the addition of LEC-8. LEC-8 is usually expressed strongly in the pharyngeal-intestinal valve and intestinal-rectal valve and is expressed weakly in intestine. However, when C. elegans were fed Escherichia coli expressing Cry5B, intestinal LEC-8::EGFP protein levels increased markedly. In contrast, LEC-8::EGFP expression triggered by Cry5B was reduced in toxin-resistant C. elegans mutants, which had mutations in genes involved in biosynthesis of glycolipids. Moreover, the LEC-8-deficient mutant was more susceptible to Cry5B than wild-type worms. These results suggest that the glycolipid-binding lectin LEC-8 contributes to host defense against bacterial infection by competitive binding to target glycolipid molecules.
引用
收藏
页码:26493 / 26501
页数:9
相关论文
共 39 条
[1]   Novel carbohydrate specificity of the 16-kDa galectin from Caenorhabditis elegans:: binding to blood group precursor oligosaccharides (type 1, type 2, Tα, and Tβ) and gangliosides [J].
Ahmed, H ;
Bianchet, MA ;
Amzel, LM ;
Hirabayashi, J ;
Kasai, K ;
Giga-Hama, Y ;
Tohda, H ;
Vasta, GR .
GLYCOBIOLOGY, 2002, 12 (08) :451-461
[2]   Sugar binding properties of the two lectin domains of the tandem repeat-type galectin LEC-1 (N32) of Caenorhabditis elegans -: Detailed analysis by an improved frontal affinity chromatography method [J].
Arata, Y ;
Hirabayashi, J ;
Kasai, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (05) :3068-3077
[3]  
BARONDES SH, 1994, J BIOL CHEM, V269, P20807
[4]   Crystal structure of the mosquito-iarvicidal toxin Cry4Ba and its biological implications [J].
Boonserm, P ;
Davis, P ;
Ellar, DJ ;
Li, J .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 348 (02) :363-382
[5]   GERMINATION OF BACILLUS-THURINGIENSIS SPORES IN BACTERIOPHAGOUS NEMATODES (NEMATODA, RHABDITIDA) [J].
BORGONIE, G ;
VANDRIESSCHE, R ;
LEYNS, F ;
ARNAUT, G ;
DEWAELE, D ;
COOMANS, A .
JOURNAL OF INVERTEBRATE PATHOLOGY, 1995, 65 (01) :61-67
[6]  
Borgonie G, 1996, FUND APPL NEMATOL, V19, P391
[7]   Microvillar membrane Microdomains exist at physiological temperature - Role of galectin-4 as lipid raft stabilizer revealed by "superrafts" [J].
Braccia, A ;
Villani, M ;
Immerdal, L ;
Niels-Christiansen, LL ;
Nystrom, BT ;
Hansen, GH ;
Danielsen, EM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (18) :15679-15684
[8]  
BRENNAN MJ, 1991, J BIOL CHEM, V266, P18827
[9]  
COX GN, 1980, GENETICS, V95, P317
[10]   Revision of the nomenclature for the Bacillus thuringiensis pesticidal crystal proteins [J].
Crickmore, N ;
Zeigler, DR ;
Feitelson, J ;
Schnepf, E ;
Van Rie, J ;
Lereclus, D ;
Baum, J ;
Dean, DH .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1998, 62 (03) :807-+