The Journal of Neuroscience, 1999:RC7:1-5
RAPID COMMUNICATION
Exacerbation of Facial Motoneuron Loss after Facial Nerve
Transection in Severe Combined Immunodeficient (scid)
Mice
Craig J.
Serpe1, 3,
Adam
P.
Kohm1,
Christopher B.
Huppenbauer1, 3,
Virginia M.
Sanders1, 2, and
Kathryn J.
Jones1, 3
Departments of 1 Cell Biology, Neurobiology, and
Anatomy and 2 Microbiology and Immunology, Loyola
University Medical Center, Illinois 60153, 3 Department of
Rehabilitation, Research and Development, Hines Veterans Administration
Hospital, Hines, Illinois 60141
The immune system functions to protect an organism against
microbial infections and may be involved in the reparative response to
nerve injury. The goal of this study was to determine whether the
immune system plays a role in regulating motoneuron survival after a
peripheral nerve injury. After a right facial nerve axotomy, facial
motoneuron (FMN) survival in C.B-17 (+/+) wild-type mice was found to
be 87 ± 3.0% of the unaxotomized left side control. In contrast,
facial nerve axotomy in C.B-17 (
/
) severe combined immunodeficient
(scid) mice, lacking functional T and B lymphocytes, resulted in an average FMN survival of 55 ± 3.5% relative to the unaxotomized left side control. This represented an ~40% decrease in
FMN survival compared with wild-type controls. The reconstitution of
scid mice with wild-type splenocytes containing T and B
lymphocytes restored FMN survival in these mice to the level of the
wild-type controls. These results suggest that immune cells associated
with acquired immunity play a role in regulating motoneuron survival after a peripheral nerve injury.
Key words:
scid; T and B Lymphocytes; neuroimmune
interactions; FMN; acquired immunity; reconstitution
Copyright © 1999 Society for Neuroscience 0270-6474/99/$05.00/0