N. Benjelloun et al., DNA FRAGMENTATION IN GLIAL-CELLS IN A CEREBRAL BIOPSY FROM A MULTIPLE-SCLEROSIS PATIENT, Cellular and molecular biology, 44(4), 1998, pp. 579-583
Multiple sclerosis is characterized by myelin destruction and oligoden
drocyte loss. The neuropathological hallmark of the disease is the pre
sence of demyelinated plaques in the central nervous system. We have r
ecently found a gliotoxic factor in MS cerebrospinal fluid which induc
es programmed cell death in vitro, in glial cells. Here we show DNA fr
agmentation and glial cell death in biopsy samples, obtained from a pa
tient who underwent surgery with suspicion of tumor, and whose disease
record, including brain autopsy, demonstrated an active multiple scle
rosis. We used the in situ TUNEL technique, a method which sensitively
detects the DNA fragmentation accompanying programmed cell death in t
issue sections, and compatible with classical fixation techniques. We
found intense DNA fragmentation in nuclei of glial cells at-or very ne
ar-to the site of demyelination. A double labeling technique showed th
at glial fibrillary associated protein positive astrocytes may undergo
programmed cell death in multiple sclerosis.