Ligation of cell surface major histocompatibility class I (MHC-I) proteins
by antibodies, or by their native counter receptor, the CD8 molecule, media
tes transduction of signals into the cells. MHC-I-mediated signaling can le
ad to both increased and decreased activity of the MHC-I-expressing cell de
pending on the fine specificity of the anti-MHC-I antibodies, the context o
f CD8 ligation, the nature and cell cycle state of the MHC-I-expressing cel
l and the presence or absence of additional cellular or humoral stimulation
. This paper reviews the biochemical, physiological and cellular events imm
ediately after and at later intervals following MHC-I ligation. It is hypot
hesized that MHC-I expression, both ontogenically and in evolution, is driv
en by a cell-mediated selection pressure advantageous to the MHC-I-expressi
ng cell. Accordingly, in addition to their role in T-cell selection and fun
ctioning, MHC-I molecules might be of importance for the maintenance of cel
lular homeostasis not only within the immune system, but also in the interp
lay between the immune system and other organ systems.