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A Dominant Complement Fixation Pathway for Pneumococcal Polysaccharides Initiated by SIGN-R1 Interacting with C1q

Authors
 Young-Sun Kang  ;  Yoonkyung Do  ;  Hae-Kyung Lee  ;  Sung Ho Park  ;  Cheolho Cheong  ;  Rebecca M. Lynch  ;  Jutta M. Loeffler  ;  Ralph M. Steinman  ;  Chae Gyu Park 
Citation
 CELL, Vol.125(1) : 47-58, 2006 
Journal Title
 CELL 
ISSN
 0092-8674 
Issue Date
2006
MeSH
Animals ; Antigen-Antibody Reactions/immunology ; CHO Cells ; Cell Adhesion Molecules/metabolism* ; Complement Activation/immunology* ; Complement C1q/immunology* ; Complement C1q/metabolism* ; Complement C3/chemistry ; Complement C3/metabolism ; Complement Pathway, Classical/immunology ; Cricetinae ; Cricetulus ; Fibroblasts/cytology ; Humans ; Lectins, C-Type/metabolism* ; Macrophages/cytology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Knockout ; Polysaccharides, Bacterial/immunology* ; Protein Binding ; Receptors, Cell Surface/metabolism* ; Spleen/cytology ; Streptococcus pneumoniae/immunology*
Abstract
The intricate system of serum complement proteins provides resistance to infection. A pivotal step in the complement pathway is the assembly of a C3 convertase, which digests the C3 complement component to form microbial binding C3 fragments recognized by leukocytes. The spleen and C3 provide resistance against blood-borne S. pneumoniae infection. To better understand the mechanisms involved, we studied SIGN-R1, a lectin that captures microbial polysaccharides in spleen. Surprisingly, conditional SIGN-R1 knockout mice developed deficits in C3 catabolism when given S. pneumoniae or its capsular polysaccharide intravenously. There were marked reductions in proteolysis of serum C3, deposition of C3 on organisms within SIGN-R1+ spleen macrophages, and formation of C3 ligands. We found that SIGN-R1 directly bound the complement C1 subcomponent, C1q, and assembled a C3 convertase, but without the traditional requirement for either antibody or factor B. The transmembrane lectin SIGN-R1 therefore contributes to innate resistance by an unusual C3 activation pathway.
Files in This Item:
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DOI
10.1016/j.cell.2006.01.046
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
Yonsei Authors
Park, Chae Gyu(박채규) ORCID logo https://orcid.org/0000-0003-1906-1308
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/111120
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