P. Ye et al., Insulin-like growth factor-I (IGF-I) protects myelination from undernutritional insult: Studies of transgenic mice overexpressing IGF-I in brain, J NEUROSC R, 62(5), 2000, pp. 700-708
Using insulin-like growth factor-I (IGF-I)-overexpressing transgenic (Tg) m
ice as a model, we have shown that IGF-I promotes myelination by increasing
the number of oligodendrocytes and stimulating the expression of myelin-sp
ecific protein genes. In the present study, we investigated whether IGF-I p
rotects myelination from undernutritional insult in Tg mice. Mice were unde
rnourished beginning from postnatal (P) day 1, a time coincident with the o
nset of transgene expression, and sacrificed at P20. Consistently with our
previous studies, brain weights of undernourished non-Tg control mice were
decreased by similar to 18%. Brain weights of undernourished IGF-I Tg mice,
however, were the same as those of well-fed control mice and much greater
than those of undernourished control mice. The expression of two major myel
in proteins [myelin basic protein (MBP) and proteolipid protein (PLP)] in c
erebral cortex (CTX) and hippocampus (HIP) was decreased by 73-92% in under
nourished control mice, as judged by Northern and Western blot hybridizatio
n. The abundances of MBP and PLP mRNAs and proteins, however, were decrease
d by only 40-70% in undernourished IGF-I Tg mice. To assess the number of o
ligodendrocytes and their precursors, antibodies specific for carbonic anhy
drase II (CAII; an oligodendrocyte marker) and NG2 (a precursor marker) wer
e used. Compared to their well-fed counterparts, undernourished control mic
e exhibited 17-30% decreases in the number of oligodendrocytes and their pr
ecursors in CTX and corpus callosum (CC), whereas well-fed IGF-I Tg mice ha
d 21-35% increases in CTX and CC. Undernourished IGF-I Tg mice exhibited ce
ll numbers similar to those of well-fed control mice. These data indicate t
hat IGF-I protects myelination from undernutrition damage during developmen
t. J. Neurosci. Res. 62: 700-708, 2000. (C) 2000 Wiley-Liss, Inc.