Deficiency of the fifth component of complement in mice with an inherited complement defect

UR Nilsson, HJ Müller-Eberhard - The Journal of experimental …, 1967 - rupress.org
UR Nilsson, HJ Müller-Eberhard
The Journal of experimental medicine, 1967rupress.org
The inherited complement deficiency of certain inbred strains of mice was shown to be due
to an isolated lack of the fifth component of complement. The protein MuB1 (or hc'), which is
present in normal mouse serum but absent from the serum of complement-deficient mice,
was shown to be immunochemically related to the fifth component of human complement
(C'5). C'5 hemolytic activity was specifically inhibited in human serum by mouse anti-MuB1
and in normal mouse serum by mouse antiserum to human C'5. Highly purified human C'5 …
The inherited complement deficiency of certain inbred strains of mice was shown to be due to an isolated lack of the fifth component of complement. The protein MuB1 (or hc'), which is present in normal mouse serum but absent from the serum of complement-deficient mice, was shown to be immunochemically related to the fifth component of human complement (C'5). C'5 hemolytic activity was specifically inhibited in human serum by mouse anti-MuB1 and in normal mouse serum by mouse antiserum to human C'5. Highly purified human C'5 reconstituted the hemolytic activity of complement-deficient mouse serum. It was, therefore, concluded that he', or MuB1, constitutes the murine analogue of the fifth component of human complement.
The MuB1 concentration in normal mouse serum was found to be subject to a sex-related variation. By quantitative precipitin analysis it was demonstrated that serum from male mice contains twice as much MuB1 as that of female mice. This difference in C'5 concentration was also detected by hemolytic assay. In addition, C'6 and C'7 were also found to be subject to sex-related variations.
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