The elution characteristics from DEAE cellulose are presented for four components of guinea pig serum, which are capable of interacting sequentially with sheep erythrocytes sensitized with antibody and the first, fourth, and second components of complement (EAC'1,4,2) to cause immune hemolysis, and information is given regarding some of the properties of these components, termed C'3c, C'3b, C'3a, and C'3d. All can react in the presence of ethylene-diaminetetraacetate, and are non-dialyzable. C'3c is quite stable at 56 degrees C, but is rapidly inactivated at low pH or by contact with hydrazine or ammonium hydroxide. C'3b is moderately heat-stable, quite susceptible to low pH, and less readily destroyed by hydrazine. C'3a is very heat-labile, but relatively stable at low pH, while C'3d is heat-labile, sensitive to low pH, and insensitive to bydrazine. EAC'1,4,2 reacts with C'3c to form EAC'1,4,2,3c, which reacts then with C'3b to give the intermediate, EAC'1,4,2,3cb. The following reaction with C'3a yields EAC'1,4,2,3cba, which reacts finally with C'3d to give EAC'1,4, 2,3cbad (E*). The first and last reactions proceed moderately well at 0 degrees C, but more rapidly at 30-37 degrees C. The reaction with C'3b is almost completely inhibited at 0 degrees C, while that involving C'3a proceeds almost as rapidly at 0 degrees C as at higher temperatures. EAC'1,4,2,3cba cells have an increased fragility as compared with the other intermediate forms. Depletion studies with purified fractions and appropriate intermediate complexes showed a high degree of depletion of C'3c, somewhat less of C'3b, and little or no depletion of C'3a from the fluid phase. Examination of a beta(1C) globulin prepared from fresh human serum revealed high C'3c and C'3b activity, and very little C'3a or C'3d.
Citing Articles
Absence of CD59 in Guinea Pigs: Analysis of the Genome Suggests the Evolution of a Pseudogene.
Boshra H, Zelek W, Hughes T, Rodriguez de Cordoba S, Morgan B
J Immunol. 2017; 200(1):327-335.
PMID: 29167230
PMC: 5739282.
DOI: 10.4049/jimmunol.1701238.
THE HEMOLYSIS OF RED CELLS FROM PATIENTS WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA BY PARTIALLY PURIFIED SUB-COMPONENTS OF THE THIRD COMPLEMENT COMPONENT.
YACHNIN S
J Clin Invest. 1965; 44:1534-46.
PMID: 14332166
PMC: 292635.
DOI: 10.1172/JCI105260.
ISOLATION OF BETA IF-GLOBULIN FROM HUMAN SERUM AND ITS CHARACTERIZATION AS THE FIFTH COMPONENT OF COMPLEMENT.
Nilsson U, MUELLER-EBERHARD H
J Exp Med. 1965; 122:277-98.
PMID: 14316946
PMC: 2138056.
DOI: 10.1084/jem.122.2.277.
THE INITIATION AND ENHANCEMENT OF HUMAN RED CELL LYSIS BY ACTIVATORS OF THE FIRST COMPONENT OF COMPLEMENT AND BY FIRST COMPONENT ESTERASE; STUDIES USING NORMAL RED CELLS AND RED CELLS FROM PATIENTS WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA.
YACHNIN S, RUTHENBERG J
J Clin Invest. 1965; 44:518-34.
PMID: 14278168
PMC: 292519.
DOI: 10.1172/JCI105165.
PH OPTIMA IN IMMUNE HEMOLYSIS: A COMPARISON BETWEEN GUINEA PIG AND HUMAN COMPLEMENT.
YACHNIN S, RUTHENBERG J
J Clin Invest. 1965; 44:149-58.
PMID: 14254250
PMC: 442027.
DOI: 10.1172/JCI105121.
DISTRIBUTION, INHERITANCE, AND PROPERTIES OF AN ANTIGEN, MUB1, AND ITS RELATION TO HEMOLYTIC COMPLEMENT.
Cinader B, DUBISKI S, Wardlaw A
J Exp Med. 1964; 120:897-924.
PMID: 14247728
PMC: 2137855.
DOI: 10.1084/jem.120.5.897.
COMPONENTS OF GUINEA PIG COMPLEMENT. I. SEPARATION OF A SERUM FRACTION ESSENTIAL FOR IMMUNE HEMOLYSIS AND IMMUNE ADHERENCE.
Nishioka K, Linscott W
J Exp Med. 1963; 118:767-93.
PMID: 14087621
PMC: 2137683.
DOI: 10.1084/jem.118.5.767.
Multiple nature of the third component of guinea-pig complement. II. Separation and description of two additional factors beta and d; preparation and characterization of four intermediate products.
WELLENSIEK H, KLEIN P
Immunology. 1965; 8(6):604-17.
PMID: 5891629
PMC: 1423544.
Multiple nature of the third component of guinea-pig complement. I. Separation and characterization of three factors a, b, and c, essential for haemolysis.
KLEIN P, WELLENSIEK H
Immunology. 1965; 8(6):590-603.
PMID: 5891628
PMC: 1423545.
Preparation and partial characterization of sheep erythrocyte-antibody-complement intermediate.
ROMMEL F, Stolfi R
Immunology. 1968; 15(4):469-79.
PMID: 5696260
PMC: 1409510.
Electrophoresis of guinea-pig complement components (C3, C5, C6, C7, C8 and C9) on polyacrylamide gel.
Okada H, Mayumi M, Mukojima T, Sekine T, Torisu M
Immunology. 1970; 18(4):493-500.
PMID: 5421032
PMC: 1455485.
Complement in skin grafting in mice.
Caren L, Rosenberg L
Immunology. 1965; 9(4):359-64.
PMID: 5320985
PMC: 1423586.
Further evidence for immune cytolysis by antibody and the first eight components of complement in the absence of C9.
Tamura N, Shimada A, Chang S
Immunology. 1972; 22(1):131-40.
PMID: 5013908
PMC: 1408206.
Immunoconglutinins in human saliva--a group of unusual IgA antibodies.
LACHMANN P, Thomson R
Immunology. 1970; 18(2):157-69.
PMID: 4984622
PMC: 1455547.
Enhancement of hemagglutination inhibition by complement.
Reno P, Hoffmann E
Infect Immun. 1972; 6(6):945-51.
PMID: 4674079
PMC: 419316.
DOI: 10.1128/iai.6.6.945-951.1972.
Multiple differentiated functions in an unusual clonal strain of hepatoma cells.
TASHJIAN Jr A, Bancroft F, Richardson U, Goldlust M, ROMMEL F, Ofner P
In Vitro. 1970; 6(1):32-45.
PMID: 4399803
DOI: 10.1007/BF02616132.
The reaction mechanism of beta-1C-globulin (C'3) in immune hemolysis.
Mullereberhard H, Dalmasso A, Calcott M
J Exp Med. 1966; 123(1):33-54.
PMID: 4159289
PMC: 2138124.
DOI: 10.1084/jem.123.1.33.
The ninth component of guinea-pig complement. Isolation and identification as an alpha 2-globulin.
Tamura N, Shimada A
Immunology. 1971; 20(3):415-25.
PMID: 4101489
PMC: 1455836.