The expression of transforming growth factor-beta 1, which has neurotrophic
effects, was investigated in 25 neonates with periventricular leukomalacia
using immunohistochemistry. In controls, transforming growth factor-beta 1
immunoreactivity was not detected in the cerebral white matter or cortex.
Of the 25 cases of periventricular leukomalacia, transforming; growth facto
r-beta 1 immunoreactivity was found in 16, and was distributed mainly in th
e cytoplasm of astrocytes, being prominent around necrotic foci in the whit
e matter. The immunoreactivity was negative or weak at the acute stage of p
eriventricular leukomalacia, and increased at the subacute stage and then d
ecreased or was absent at the chronic stage. Astrocytes that were moderatel
y or markedly positive for transforming growth factor-beta 1 were not found
before 27 weeks' gestation, but were observed after 32 weeks' gestation in
the white matter of the brains of neonates with periventricular leukomalac
ia. Transforming growth factor-beta 1 expression tended to be more obvious
in focal periventricular leukomalacia than in widespread or diffuse periven
tricular leukomalacia. Our results suggest that transforming growth factor-
beta 1 could be involved in the delayed glial response rather than the init
ial glial activation, and could play a role in the inhibition and repair of
injury in periventricular leukomalacia. Exogenous transforming growth fact
or-beta 1 could have therapeutic potential for periventricular leukomalacia
.