Gf. Tseng et al., PERINEURONAL MICROGLIAL REACTIVITY FOLLOWING PROXIMAL AND DISTAL AXOTOMY OF RAT RUBROSPINAL NEURONS, Brain research, 715(1-2), 1996, pp. 32-43
Microglial reactivity in the red nucleus of rats was studied following
upper cervical and lower thoracic rubrospinal tractotomy using the le
ctin binding method. Following axotomy, the contralateral nucleus cont
aining the axotomized neurons was identified using the retrograde trac
er Fast blue. It was subdivided into dorsomedial (DM) and ventrolatera
l (VL) portions known to project to the cervical and lumbar spinal cor
d, respectively. Lectin-labeled microglial cells and processes on the
contralateral as well as in the ipsilateral nucleus were then quantifi
ed. An early and a late increase in microglial reactivity was observed
in the nucleus at 2-5 days and 2-8 weeks following thoracic and cervi
cal tractotomy with the latter producing a more pronounced reactivity.
In rats subjected to thoracic axotomy, a similar microglial increase
also occurred in the intact contralateral DM nuclear area suggesting t
he possible action of diffusible factor(s) that might have triggered t
he microglial activation from the axotomized VL nuclear area. The unin
jured ipsilateral nucleus also exhibited a similar pattern of microgli
al reactivity irrespective of the number of ipsilaterally projecting n
eurons following both cervical and thoracic axotomy. This could have b
een elicited by the retrograde influence from the denervated targets c
arried by the intact rubrospinal fibers of the opposite side since man
y of them in fact terminate bilaterally (Antal, M. et al., J. Comp. Ne
urol., 325 (1992) 22-37). In all the axotomized or intact nucleus, mic
roglial processes did not appear to surround neuronal cell bodies. The
characteristic responses of microglial cells in the red nucleus may b
e related to the failure of rubrospinal neurons to regenerate followin
g the severance of their axons.