Hereditary deficiencies in complement C5 are associated with intensified neurodegenerative responses that implicate new roles for the C-system in neuronal and astrocytic functions

Neurobiol Dis. 1996;3(3):197-204. doi: 10.1006/nbdi.1996.0020.


Possible roles of the complement (C) system in the normal and injured brain were explored with inbred mice that carried a frameshift mutation in the C5 gene. A congenic pair was used: the C5-sufficient (C5+) B10.D2/nSnJ strain with the functional allele (Hc1) from the C57BL/10J donor strain was compared with the C5-deficient (C5-) B10.D2/oSnJ with the Hc0 allele from the C5-deficient DBA/2J donor strain. In response to the excitotoxin kainic acid (KA), C5- mice had more hippocampal pyramidal neuron death and greater induction of astrocyte mRNAs (GFAP, apoE, apoJ). In primary astrocyte cultures from unlesioned mice, an inflammatory stimulus (LPS) caused greater production of IL-6 and TNF production in C5- mice. These enhanced responses to KA and LPS suggest that hereditary C5 deficits modify responses to neurodegenerative stimuli of neurons and astrocytes. Moreover, unlesioned C5- mice had smaller input-output slopes for the NMDA component of the EPSP amplitude, but enhanced the Ca(+2)-dependent AMPA binding. Thus, C5 deficits also modify basal properties of glutamatergic neurotransmission that pertain to synaptic plasticity. These findings are also discussed in relation to roles of the C-system in Alzheimer disease (AD). C5 deficiencies may also be considered in the choice of strains as transgene hosts and for genetic analysis of normal and pathological brain functions. In recent transgenic studies for AD, C5- hosts showed greater neurodegeneration, consistent with the present data. These pleiotropic associations of C5 deficiency indicate roles for the C-system in neurodegeneration, but also in normal neural functions.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Astrocytes / drug effects
  • Astrocytes / metabolism
  • Astrocytes / physiology*
  • Cell Death
  • Cells, Cultured
  • Complement C5 / deficiency*
  • Complement C5 / physiology*
  • Electrophysiology
  • Hippocampus / cytology
  • Hippocampus / drug effects
  • Interleukin-6 / biosynthesis
  • Kainic Acid / pharmacology
  • Lipopolysaccharides / pharmacology
  • Mice
  • Mice, Inbred Strains / genetics
  • Nerve Degeneration / physiology*
  • Pyramidal Cells / drug effects
  • Pyramidal Cells / physiology*
  • RNA, Messenger / metabolism
  • Receptors, N-Methyl-D-Aspartate / physiology
  • Tumor Necrosis Factor-alpha / biosynthesis
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid / metabolism


  • Complement C5
  • Interleukin-6
  • Lipopolysaccharides
  • RNA, Messenger
  • Receptors, N-Methyl-D-Aspartate
  • Tumor Necrosis Factor-alpha
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid
  • Kainic Acid