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Volume 17, Number 9,
Issue of May 1, 1997
pp. 3096-3111
Copyright ©1997 Society for Neuroscience
Differential Expression of Connexins during Neocortical
Development and Neuronal Circuit Formation
Received Dec. 19, 1996; revised Feb. 7, 1997; accepted Feb. 12, 1997.
B. Nadarajah1,
A. M. Jones2,
W. H. Evans2, and
J. G. Parnavelas1
1 Department of Anatomy and Developmental
Biology, University College London, London WC1E 6BT, United Kingdom,
and 2 Department of Medical Biochemistry, University of
Wales College of Medicine, Cardiff CF4 4XN, United Kingdom
Gap junctions are membrane channels that mediate the direct
passage of ions and molecules between adjacent cells. Recent tracer coupling and optical recording studies have revealed the presence of
gap junction-mediated communication between neurons during neocortical
development. We have visualized gap junctions in the developing rat
cerebral cortex with electron microscopy and studied the pattern of
expression and cellular localization of connexins 26, 32, and 43 that
take part in their formation. We found that these connexins (Cxs) are
expressed differentially during development, and their patterns of
expression are correlated with important developmental events such as
cell proliferation, migration, and formation of cortical neuronal
circuits. Specifically, we observed that the developmental profile of
Cx 26 during the first 3 weeks of postnatal life matched closely the
development of neuronal coupling, suggesting that coupled neurons use
this gap junction protein during circuit formation in the cortex. The
subsequent diminution of Cx 26 was mirrored by an increase in Cx 32 immunoreactivity, which became pronounced at the late stages of
cortical maturation. In contrast, Cx 43 was localized in the cortex
throughout the period of development. Its localization in radial glial
fibers closely associated with migrating neurons suggests that this Cx may be involved in neuronal migration.
Key words:
connexin 26;
connexin 32;
connexin 43;
gap junctions;
development;
neocortex;
immunocytochemistry;
electron microscopy
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