We have previously demonstrated that mice deficient in ICAM-1 and P-selecti
n (ICAM-1/PS-/-) have improved functional recovery after spinal cord injury
(SCI), compared to injured controls. In this study the spinal cords from w
ild-type and ICAM-1/PS-/- mice were evaluated histopathologically 14 days a
fter severe compression-type SCI. Following injury there was an atrophy of
the spinal cord. Significant sparing of total cross-sectional area was note
d in ICAM-1/PS-/- mice compared to injured controls at the site of compress
ion and in the distal peri-injury zone. Likewise, significant preservation
of white matter area, as measured by Luxol staining, was found in mutant mi
ce at the site of injury and in the proximal peri-injury zone. Gray matter
damage was investigated by microtubule-associated protein 2 immunohistochem
istry. Following severe SCI, a trend of gray matter sparing was noticed in
ICAM-1/PS-/- animals. Quantitation of iba1 immunohistochemistry revealed th
at microglial reaction was significantly suppressed in the mutant animals.
Astroglial reaction, visualized by GFAP immunostaining, did not differ betw
een groups. Our results indicate that ICAM-1 and P-selectin are involved in
autodestructive events provoked by the initial injury but the precise unde
rlying mechanisms remain obscure.