Salivary agglutinin/gilycoprotein-340/DMBT1: a single molecule with variable composition and with different functions in infection, inflammation and cancer

被引:95
作者
Ligtenberg, Antoon J. M.
Veerman, Enno C. I.
Nieuw Amerongen, Arie V.
Mollenhauer, Jan
机构
[1] Free Univ Amsterdam, Acad Ctr Dent, Dept Oral Biochem, NL-1081 BT Amsterdam, Netherlands
[2] German Canc Res Ctr, Div Mol Genome Anal, D-69120 Heidelberg, Germany
关键词
innate immunity; mucosal defence; saliva; tumour suppression;
D O I
10.1515/BC.2007.158
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
Salivary agglutinin (SAG), lung glycoprotein-340 (gp-340) and Deleted in Malignant Brain Tumours 1 (DMBT1) are three names for identical proteins encoded by the dmbt1 gene. DMBT1/SAG/gp-340 belongs to the scavenger receptor cysteine-rich (SRCR) superfamily of proteins, a superfamily of secreted or membrane-bound proteins with SRCR domains that are highly conserved down to sponges, the most ancient metazoa. On the one hand, DMBT1 may represent an innate defence factor acting as a pattern recognition molecule. It interacts with a broad range of pathogens, including cariogenic streptococci and Helicobacter pylori, influenza viruses and HIV, but also with mucosal defence proteins, such as IgA, surfactant proteins and MUC5B. Stimulation of alveolar macrophage migration, suppression of neutrophil oxidative burst and activation of the complement cascade point further to an important role in the regulation of inflammatory responses. On the other hand, DMBT1 has been demonstrated to play a role in epithelial and stem cell differentiation. Inactivation of the gene coding for this protein may lead to disturbed differentiation, possibly resulting in tumour formation. These data strongly point to a role for DMBT1 as a molecule linking innate immune processes with regenerative processes.
引用
收藏
页码:1275 / 1289
页数:15
相关论文
共 153 条
[1]   Complete genome sequence of the apicomplexan, Cryptosporidium parvum [J].
Abrahamsen, MS ;
Templeton, TJ ;
Enomoto, S ;
Abrahante, JE ;
Zhu, G ;
Lancto, CA ;
Deng, MQ ;
Liu, C ;
Widmer, G ;
Tzipori, S ;
Buck, GA ;
Xu, P ;
Bankier, AT ;
Dear, PH ;
Konfortov, BA ;
Spriggs, HF ;
Iyer, L ;
Anantharaman, V ;
Aravind, L ;
Kapur, V .
SCIENCE, 2004, 304 (5669) :441-445
[2]   Toll-like receptors in the induction of the innate immune response [J].
Aderem, A ;
Ulevitch, RJ .
NATURE, 2000, 406 (6797) :782-787
[3]   Terminal differentiation of intercalated cells: The role of Hensin [J].
Al-Awqati, Q .
ANNUAL REVIEW OF PHYSIOLOGY, 2003, 65 :567-583
[4]   Oral microbiota associated with hyposalivation of different origins [J].
Almståhl, A ;
Wikström, M ;
Stenberg, I ;
Jakobsson, A ;
Fagerberg-Mohlin, B .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 2003, 18 (01) :1-8
[5]   Identification and characterization of large galactosyltransferase gene families: galactosyltransferases for all functions [J].
Amado, M ;
Almeida, R ;
Schwientek, T ;
Clausen, H .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1999, 1473 (01) :35-53
[6]   ROLE OF CATIONS AND IGA IN SALIVA-MEDIATED AGGREGATION OF PSEUDOMONAS-AERUGINOSA IN CYSTIC-FIBROSIS PATIENTS [J].
ARMSTRONG, EA ;
ZIOLA, B ;
HABBICK, BF ;
KOMIYAMA, K .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1993, 22 (05) :207-213
[7]  
ARNEBERG P, 1976, SCAND J DENT RES, V84, P362
[8]   CD6-ligand interactions: a paradigm for SRCR domain function? [J].
Aruffo, A ;
Bowen, MA ;
Patel, DD ;
Haynes, BF ;
Starling, GC ;
Gebe, JA ;
Bajorath, J .
IMMUNOLOGY TODAY, 1997, 18 (10) :498-504
[9]   Porphyromonas gingivalis lipopolysaccharide:: an unusual pattern recognition receptor ligand for the innate host defense system [J].
Bainbridge, BW ;
Darveau, RP .
ACTA ODONTOLOGICA SCANDINAVICA, 2001, 59 (03) :131-138
[10]   Salivary agglutinin/DMBT1SAG expression is up-regulated in the presence of salivary gland tumors [J].
Bikker, FJ ;
van der Wal, JE ;
Ligtenberg, AJM ;
Mollenhauer, J ;
de Blieck-Hogervorst, JMA ;
van der Waal, I ;
Poustka, A ;
Amerongen, AVN .
JOURNAL OF DENTAL RESEARCH, 2004, 83 (07) :567-571