Insulin-like growth factor-1 (IGF-1) is essential to hippocampal neurogenesis and the neuronal response to
hypoxia/
ischemia injury. IGF (IGF-1 and -2) signaling is mediated primarily by the type 1 IGF receptor (IGF-1R) and modulated by six high-affinity
binding proteins (
IGFBP) and the type 2 IGF receptor (IGF-2R), collectively termed IGF system
proteins. Defining the precise cells that express each is essential to understanding their roles. With the exception of
IGFBP-1, we found that mouse hippocampus expresses
mRNA for each of these
proteins during the first 2 weeks of postnatal life. Compared to postnatal day 14 (P14),
mRNA abundance at P5 was higher for
IGF-1,
IGFBP-2, -3, and -5 (by 71%, 108%, 100%, and 98%, respectively), lower for
IGF-2, IGF-2R, and
IGFBP-6 (by 65%, 78%, and 44%, respectively), and unchanged for IGF-1R and
IGFBP-4. Using
laser capture microdissection (LCM), we found that granule neurons and pyramidal neurons exhibited identical patterns of expression of
IGF-1, IGF-1R, IGF-2R,
IGFBP-2, and -4, but did not express other IGF system genes. We then compared IGF system expression in mature granule neurons and their progenitors. Progenitors exhibited higher
mRNA levels of
IGF-1 and IGF-1R (by 130% and 86%, respectively), lower levels of IGF-2R (by 72%), and similar levels of
IGFBP-4. Our data support a role for IGF in hippocampal neurogenesis and provide evidence that IGF actions are regulated within a defined in vivo milieu.