The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ji, Y. H.
Right arrow Articles by Kawakami, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ji, Y. H.
Right arrow Articles by Kawakami, M.

The Journal of Immunology, Vol 141, Issue 12 4271-4275, Copyright © 1988 by American Association of Immunologists


ARTICLES

The C4 and C2 but not C1 components of complement are responsible for the complement activation triggered by the Ra-reactive factor

YH Ji, M Matsushita, H Okada, T Fujita and M Kawakami
Department of Molecular Biology, School of Medicine, Kitasato University, Kanagawa-ken, Japan.

Ra-reactive factors (RaRF) are the name of a group of C-dependent bactericidal factors that bind specifically to Ra chemotype strains of Salmonella. These factors are present in the sera of a wide variety of vertebrates and have common characteristics. Here we investigate the C components required for the C activation induced by mouse RaRF, by using hemolysis of Ra LPS-coated E (ELPS) as a model system. It was found that C1-depleted and C1q-depleted sera were as effective as the undepleted serum in the lysis of ELPS sensitized with RaRF. Addition of the C1 component or C1q subcomponent to the depleted sera did not increase the effect. On the other hand, C4 and C2 components were found to be essential for the lysis of RaRF-sensitized ELPS. Activities of C4 and C2 remained on the sensitized cells even after washing the cells, suggesting that the classical C3 convertase, C4b2a, is generated on the RaRF-sensitized ELPS.


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
M. Arora, E. Munoz, and A. J. Tenner
Identification of a Site on Mannan-binding Lectin Critical for Enhancement of Phagocytosis
J. Biol. Chem., November 9, 2001; 276(46): 43087 - 43094.
[Abstract] [Full Text] [PDF]


Home page
Int ImmunolHome page
M. Takahashi, Y. Endo, T. Fujita, and M. Matsushita
A truncated form of mannose-binding lectin-associated serine protease (MASP)-2 expressed by alternative polyadenylation is a component of the lectin complement pathway
Int. Immunol., May 1, 1999; 11(5): 859 - 863.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
C. M. Stover, S. Thiel, M. Thelen, N. J. Lynch, T. Vorup-Jensen, J. C. Jensenius, and W. J. Schwaeble
Two Constituents of the Initiation Complex of the Mannan-Binding Lectin Activation Pathway of Complement Are Encoded by a Single Structural Gene
J. Immunol., March 15, 1999; 162(6): 3481 - 3490.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
C. Suankratay, X.-H. Zhang, Y. Zhang, T. F. Lint, and H. Gewurz
Requirement for the Alternative Pathway as Well as C4 and C2 in Complement-Dependent Hemolysis Via the Lectin Pathway
J. Immunol., March 15, 1998; 160(6): 3006 - 3013.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1988 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1988 by The American Association of Immunologists, Inc. All rights reserved.