Oligodendrocyte cell migration is required for the development of the nervo
us system and the repopulation of demyelinated lesions in the adult central
nervous system. We have investigated the role of the calcium-dependent adh
esion molecules, the cadherins, in oligodendrocyte-astrocyte interaction an
d oligodendrocyte progenitor migration. Immunostaining demonstrated the exp
ression of N-cadherin on the surfaces of both oligodendrocytes and astrocyt
es, and oligodendrocyte-like cells adhered to and spread on N-cadherin subs
trates. The blocking of cadherin function by antisera or specific peptides
reduced adhesion of oligodendroglia to astrocyte monolayers, diminished con
tact time between oligodendrocyte processes and individual astrocytes, and
significantly increased the migration of oligodendrocyte-like cells on astr
ocyte monolayers. Furthermore, a soluble cadherin molecule without adhesive
properties increased oligodendroglial proliferation on various extracellul
ar matrix substrates. These data suggest that cadherins are at least partia
lly responsible for the poor migration-promoting properties of astrocytes a
nd that decreasing cell-cell adhesion might effect repopulation of demyelin
ated multiple sclerosis lesions by oligodendrocyte progenitors.