The transmissible spongiform encephalopathies are neurodegenerative di
sorders which include Creutzfeldt-Jakob disease in humans, and scrapie
and bovine spongiform encephalopathy in animals. A major component of
the infectious agent responsible for these diseases is considered to
be a post-translationally modified form of a host-encoded glycoprotein
PrPc, termed PrPSc. While PrPc is abundantly expressed in tissues of
the central nervous system (CNS), little is known about its normal fun
ction. The expression of PrPc is not restricted to the CNS, as this pr
otein can also be detected in the lymphoid tissues of mice and sheep.
In this report we demonstrate that resting murine splenic lymphocytes
express PrPc protein on their cell membranes. Furthermore, expression
of PrPc was significantly enhanced following in vitro stimulation with
the non-specific T-cell mitogen concanavalin A (Con A). Genetically e
ngineered mice with an inactive PrPc gene (PrP(-/-)mice), were utilize
d to investigate the involvement of PrPc in lymphocyte activation. Exp
eriments revealed that the Con A-induced proliferation of lymphocytes
from PrP(-/-)mice was significantly reduced to approximate to 50-80% t
hat of wild-type (PrP+/+) mice 48 hr post-stimulation. These findings
demonstrate an important role for PrPc in extra-neuronal tissues and s
uggest that PrPc is a lymphocyte surface molecule that participates in
T-cell activation.