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PMID: 3894085 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

The cobra complement system: I. The alternative pathway of activation.

Developmental and comparative immunology ·Vol. 9 ·No. 2 ·1985-00-00 ·Pages 311-25

Vogel CW, Müller-Eberhard HJ

Abstract

The complement system of the cobra snake is of particular interest because cobra venom contains cobra venom factor (CVF), a protein that is related to C3 and forms a stable C3 convertase with mammalian Factor B. We investigated the alternative pathway of cobra complement. Cobra plasma lysed erythrocytes in presence of Mg-EGTA of some mammalian species, but not cobra erythrocytes. The hemolytic activity was inhibited by EDTA and destroyed by heating. Preincubation of cobra plasma with alternative pathway activators (zymosan, inulin, lipopolysaccharide), with small nucleophiles (methylamine, hydrazine), or with chaotropes (KSCN) abrogated the hemolytic activity. The activity of cobra plasma was not affected by CVF. Cobra plasma also lysed EAC1423 cells in presence of EDTA but not EAC142 cells (prepared with sheep erythrocytes, rabbit antibody, and human complement proteins) indicating the presence of C5 in cobra plasma that is susceptible to activation by the human C5 convertase. These results indicate that the cobra has a complement system with an alternative pathway very similar to mammalian complement.

MeSH Terms
Animals Complement Activation/drug effects Complement C3/immunology Complement C5/immunology Complement Pathway, Alternative/drug effects Elapid Venoms/immunology Erythrocytes/immunology Hemolysis Humans In Vitro Techniques Methylamines/pharmacology Phylogeny Snakes/immunology Species Specificity
Chemicals
Complement C3 Complement C5 Elapid Venoms Methylamines cobra venom factor methylamine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Vogel C W
Müller-Eberhard H J
Article Info
Journal
Developmental and comparative immunology
Abbr.
Dev Comp Immunol
ISSN
0145-305X
Published
1985-00-00
Pages
311-25
Language
English
Region
United States
NLM ID
7708205
Subset
IM
Grants
NIAID NIH HHS · AI 17354 · United States
NCI NIH HHS · CA 27489 · United States
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