INTERACTIONS BETWEEN GLIAL PROGENITORS AND BLOOD-VESSELS DURING EARLYPOSTNATAL CORTICOGENESIS - BLOOD-VESSEL CONTACT REPRESENTS AN EARLY-STAGE OF ASTROCYTE DIFFERENTIATION
M. Zerlin et Je. Goldman, INTERACTIONS BETWEEN GLIAL PROGENITORS AND BLOOD-VESSELS DURING EARLYPOSTNATAL CORTICOGENESIS - BLOOD-VESSEL CONTACT REPRESENTS AN EARLY-STAGE OF ASTROCYTE DIFFERENTIATION, Journal of comparative neurology, 387(4), 1997, pp. 537-546
The post-neurogenic period in the mammalian neocortex is characterized
by the growth of astrocyte and oligodendrocyte populations and their
incorporation into the network of the developing central nervous syste
m (CNS). Many of these glial cells originate as progenitors in the sub
ventricular zone (SVZ) and then migrate into white and gray matter bef
ore differentiating. What determines the specific cellular fate of pro
genitors in vivo is not known, however. In examining the early stages
of gliogenesis from progenitors in the SVZ, we noted that interactions
with cortical blood vessels took place at what appeared to be an earl
y stage of glial differentiation. We have examined in more detail the
interactions of progenitors with blood vessels in the early postnatal
rat neocortex after labeling progenitors in vivo with a LacZ-encoding
retrovirus. These early interactions are accompanied by an increase in
intermediate filament expression, consistent with astrocytic differen
tiation. Because astrocytes interact with blood vessels and pia, we su
ggest that such contact represents an early stage in astrocytic differ
entiation. Furthermore, since angiogenesis and astrogenesis occur over
a similar period, the growth of blood vessels may even play a role in
the selection of astrocytic fate by a progenitor. As vessel growth sl
ows, fewer progenitors may be directed toward an astrocyte fate, allow
ing more to differentiate into oligodendrocytes, perhaps explaining th
e shift from astrocyte genesis to oligodendrocyte genesis during early
postnatal cortical development. J. Comp. Neurol. 387:537-546, 1997. (
C) 1997 Wiley-Liss, Inc.