Collectins: Collectors of microorganisms for the innate immune system

被引:76
作者
Lu, JH
机构
[1] Department of Biochemistry, Faculty of Medicine, National University of Singapore, Singapore 119260
关键词
D O I
10.1002/bies.950190610
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
Collectins are a group of multimeric proteins mostly consisting of 9-18 polypeptides organised into either 'bundle-of-tulips' or 'X-like' overall structures. Each polypeptide contains a short N-terminal segment followed by a collagenlike sequence and then by a C-terminal lectin domain. A collectin molecule is assembled from identical or very similar polypeptides by disulphide bonds at the N-terminal segment, formation of triple he[ices in the collagen-like region and clusters of three lectin domains at the peripheral ends of triple helices. These proteins can bind to sugar residues on microorganisms via the peripheral lectin domains and subsequently interact, via the collagen-like triple-helices, with receptor(s) on phagocytes and/or the complement system to bring about the killing and clearance of the targets without the involvement of antibodies. The collectins can also bind to phagocyte receptor(s) to enhance phagocytosis mediated by other phagocytic receptors. Lack, or low levels, of collectin expression can lead to higher susceptibility to infections, especially during childhood when specific immunity has not fully developed. Therefore, the co(lectins play important roles in the enhancement of innate immunity.
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页码:509 / 518
页数:10
相关论文
共 79 条
[71]  
THIEL S, 1996, MOL IMMUNOL S1, V33, P91
[72]   STRUCTURAL COMPARISON OF RECOMBINANT PULMONARY SURFACTANT PROTEIN SP-A DERIVED FROM 2 HUMAN CODING SEQUENCES - IMPLICATIONS FOR THE CHAIN COMPOSITION OF NATURAL HUMAN SP-A [J].
VOSS, T ;
MELCHERS, K ;
SCHEIRLE, G ;
SCHAFER, KP .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1991, 4 (01) :88-94
[73]   MACROMOLECULAR ORGANIZATION OF NATURAL AND RECOMBINANT LUNG SURFACTANT PROTEIN SP-28-36 - STRUCTURAL HOMOLOGY WITH THE COMPLEMENT FACTOR CLQ [J].
VOSS, T ;
EISTETTER, H ;
SCHAFER, KP ;
ENGEL, J .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 201 (01) :219-227
[74]   IMMUNOCYTOCHEMICAL LOCALIZATION OF THE MAJOR SURFACTANT APOPROTEINS IN TYPE-II CELLS, CLARA CELLS, AND ALVEOLAR MACROPHAGES OF RAT LUNG [J].
WALKER, SR ;
WILLIAMS, MC ;
BENSON, B .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1986, 34 (09) :1137-1148
[75]   FUNCTION AND REGULATION OF EXPRESSION OF PULMONARY SURFACTANT-ASSOCIATED PROTEINS [J].
WEAVER, TE ;
WHITSETT, JA .
BIOCHEMICAL JOURNAL, 1991, 273 :249-264
[76]   TRIMERIC STRUCTURE OF A C-TYPE MANNOSE-BINDING PROTEIN [J].
WEIS, WI ;
DRICKAMER, K .
STRUCTURE, 1994, 2 (12) :1227-1240
[77]   THE MURINE MANNOSE-BINDING PROTEIN GENES (MBL-1 AND MBL-2) LOCALIZE TO CHROMOSOME-14 AND CHROMOSOME-19 [J].
WHITE, RA ;
DOWLER, LL ;
ADKISON, LR ;
EZEKOWITZ, RAB ;
SASTRY, KN .
MAMMALIAN GENOME, 1994, 5 (12) :807-809
[78]   ISOLATION AND CHARACTERIZATION OF THE HUMAN PULMONARY SURFACTANT APOPROTEIN GENE [J].
WHITE, RT ;
DAMM, D ;
MILLER, J ;
SPRATT, K ;
SCHILLING, J ;
HAWGOOD, S ;
BENSON, B ;
CORDELL, B .
NATURE, 1985, 317 (6035) :361-363
[79]  
WHITSETT JA, 1985, J BIOL CHEM, V260, P5273