Am. J. Respir. Cell Mol. Biol., Vol 12, No. 1, Jan 1995, 56-64.
Regulation of the insulin-like growth factor system during normal rat lung development
BM Moats-Staats, WA Price, L Xu, HW Jarvis and AD Stiles
Department of Pediatrics, University of North Carolina at Chapel Hill.
Insulin-like growth factor (IGF)-I and IGF-II are small peptide growth
factors that interact with a specific membrane receptor, the type 1 IGF
receptor, to stimulate cellular proliferation and/or differentiation. The
actions of these growth factors and their availability to their receptors
are modulated by specific binding proteins, IGF binding protein (IGFBP)-1
through -6, which together with the IGFs and IGF receptors form the IGF
system. We have analyzed RNA extracted from fetal (gestation day 16 [E16]
through 22 [E22]) and adult (60-day-old) rat lung for expression of each
component of the IGF system. IGF-I and - II RNAs are expressed throughout
fetal development. IGF-I mRNA remained relatively constant in fetal and
adult lung, whereas IGF-II RNA decreased in later gestation to levels below
detection by Northern analyses in adult lung. Type 1 IGF receptor
expression varied little through all ages studied, whereas the type 2 IGF
receptor RNA displayed developmental regulation with a decline in
expression with advancing age. IGFBP-1 transcripts were not detected in
fetal or adult lung. IGFBP-2 RNA was expressed from E16 to E22, although
its abundance decreased in late gestation and in adult lung, with the
lowest levels of expression on day E22. IGFBP-3, -4, and -5 had similar
profiles of RNA abundance, with fetuses at ages E21 and E22 displaying
higher levels of transcript abundance as compared with those aged E17 to
E20; the lowest RNA abundance was seen at E20.(ABSTRACT TRUNCATED AT 250
WORDS)
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Copyright © 1995 American Thoracic Society.
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