Pa. Felts et Kj. Smith, CHANGES IN THE DISTRIBUTION OF A CALCIUM-DEPENDENT ATPASE DURING DEMYELINATION AND REMYELINATION IN THE CENTRAL-NERVOUS-SYSTEM, Journal of neurocytology, 25(3), 1996, pp. 171-180
A calcium-adenosine triphosphatase (Ca2+-ATPase) activity expressed by
CNS nerve fibres has been examined during demyelination and remyelina
tion in rats, 21-26 days after an intraspinal injection of ethidium br
omide. The Ca2+-ATPase distribution was determined cytochemically, usi
ng a technique believed primarily to reflect the presence of ecto-ATPa
ses. We confirm that in normal nerve fibres Ca2+-ATPase activity was p
resent on the external surface of the myelin sheath, and on the axolem
ma at the nodes of Ranvier. Labelling of the internodal axolemma was r
estricted to small, scattered, punctate regions. However, following de
myelination the Ca2+-ATPase activity was expressed continuously along
both the exposed, previously internodal axolemma of entirely naked axo
ns, and it was particularly prominent at sites of contact between axon
s and glial-cell processes. During remyelination (which in this lesion
is accomplished predominantly by Schwann cells) the proportion of the
axonal surface exhibiting Ca2+-ATPase activity decreased in concert w
ith the progressive thickening of the new myelin sheath. The non-myeli
n forming plasmalemma of Schwann cells was positive for the Ca2+ ATPas
e activity, but activity was abruptly lost at the site of compaction b
etween the inner and outer leaflets of the forming myelin sheath. Ecto
-ATPase activity is a property of some cell adhesion molecules, and it
follows that the changes observed in the distribution of ATPase activ
ity in this study may reflect changes in the axolemma which are import
ant for the successful repair of the lesion by remyelination. The ATPa
se activity may, for example, reflect the changing distribution of mol
ecules important in aiding axo-glial recognition and the establishment
of axo-glial contacts.