We compared migration of systemically injected microglia into normal brain
vs. ischaemic brain using a model of ischaemic hippocampal lesion. Microgli
a were labeled by a fluorescent dye using our standard phagocytosis procedu
re of microscopic particles and then injected intra-arterially into Mongoli
an gerbils subjected to ischaemia reperfusion neuronal injury. Delayed deat
h of pyramidal neurons was confirmed by conventional histological analysis
and dUTP nick end labeling (TUNEL) method. Clusters of dye-tagged cells mig
rating into the hippocampal ischaemic lesions were confirmed histochemicall
y to be microglia. Since peripherally injected microglia exhibit specific a
ffinity for ischaemic brain lesions and does not exacerbate ischaemic neuro
nal injury in the present model, we suggest that microglia may have a poten
tial to be used as a piggy-back ride to deliver therapeutic genes and/or dr
ugs for CNS repair following transitory global ischaemic insult. (C) 1999 E
lsevier Science Ireland Ltd. All rights reserved.