Mr. Del Bigio et al., Glial swelling with eosinophilia in human post-mortem brains: a change indicative of plasma extravasation, ACT NEUROP, 100(6), 2000, pp. 688-694
Swollen, intensely eosinophilic glial cells are often observed in the vicin
ity of hemorrhagic lesions in post-mortem human brains. We sought to determ
ine the nature of this change. Thirty adult human brains removed at autopsy
and three surgical specimens were obtained 6h to 60 days following a hemor
rhagic event. They were subjected to a battery of histochemical and immunoh
istochemical stains. The swollen cells, which were observed in the majority
of autopsy specimens in which hemorrhage had occurred within the previous
9 days, stained intensely red with Masson stain and were immunoreactive for
IgG, IgM, IgA, and fibrinogen. Some were also immunoreactive for glial fib
rillary acidic protein, particularly in subpial and subependymal areas, if
the lesions were more than 3 days old. In white matter some of the cells we
re immunoreactive for CNPase. There was no labeling with markers for macrop
hage/microglial cells. The absence of DNA fragment detection by TUNEL sugge
sts that the cells were not dying. Mild glial cytoplasmic eosinophilia with
out swelling was observed in surgical specimens. No eosinophilic swollen gl
ia were seen in perfusion-fixed rat brains with experimental intracerebral
hemorrhage, although they were seen in rat brains that were not promptly fi
xed. We conclude that human macroglia, including astrocytes and oligodendro
cytes, ingest plasma proteins that have been released into brain parenchyma
. This likely represents a homeostatic mechanism that maintains the composi
tion of the extracellular environment. If the tissue is not promptly fixed
the cells become more swollen and eosinophilic.