It has been shown recently in mouse model systems that the Id proteins play
a critical role in angiogenesis both during embryogenesis and tumor format
ion. The Id proteins are intracellular proteins that inhibit the activity o
f differentiation-promoting transcription factors and thereby block differe
ntiation and promote cell cycle progression. Loss of Id function in mice le
ads to premature neural differentiation and withdrawal from the cell cycle
in neurons and also the execution of an aberrant differentiation cascade in
endothelial cells. This latter event is associated with a midgestational b
rain hemorrhage when Id dosage is sufficiently low. Partial reduction in Id
levels spares the endothelium in the brain but adults born fail to support
the vascularization of tumors. Through the analysis of these phenotypes an
d characterization of altered gene expression in the Id knockout endotheliu
m, subdivisions in the angiogenic process are being defined which may lead
to selective anti-angiogenic treatments in the management of human disease.
(C) 2001, Elsevier Science Inc.