In the brain, in vivo as in vitro, glial cells represent the main cell
population which communicates through intercellular channels forming
gap junctions. These cells, and specially the astrocytes, also express
a large variety of ionic channels and membrane receptors. The combina
tion of biochemical, immunological and electrophysiological techniques
has allowed to determine that connexin 32 is present in oligodendrocy
tes while connexin 43 is the major junctional protein in astrocytes. T
he conductance and permeability of gap junctions in astrocytes are con
trolled by endogenous compounds released from izeurorzs or endothelial
cells. This suggests that gap junctional communication in astrocyte n
etworks exhibits some degree of plasticity and are under the control o
f other brain cell populations. The expression of connexins and the re
gulation of junctional permeability in astrocytes may contribute to se
veral glial functions such as intercellular calcium signalling and met
abolic trafficking within the brain.