Previously, we have demonstrated that integrin-associated protein (IAP) mRN
A level is approximately fourfold higher in rats showing good. retention pe
rformance (600 sec) than rats showing poor retention performance (<80 sec)
in an inhibitory avoidance learning paradigm. In the present study, we have
used. the gene-targeted IAP-defident mice to further investigate the role
of IAP involved in memory formation and hippocampal long-term potentiation
(LTP) in vivo. Results revealed that there was a significant impairment in
memory retention and a significant reduction in the magnitude of LTP in IAP
-deficient mice when compared with the wild-type and heterozygote mice, whe
reas the wild-type and heterozygote animals did not show marked, difference
s on these measures; Furthermore, the impairment in retention performance o
f IAP-deficient mice was not due to different sensitivities of these animal
s to the electric shock. When we examined locomotor activity and rotarod tr
eadmill performance, no differences were observed among these three groups
of animals either. Western blot analysis confirmed the lack of IAP protein
in IAP-deficient mice, whereas IAP expression was similar in both the wild-
type and heterozygote controls. These results together demonstrate that IAP
plays an important role in the process of memory formation and synaptic pl
asticity in mice.