Radiation‐induced apoptosis of oligodendrocytes and its association with increased ceramide and down‐regulated protein kinase B/Akt activity

Abstract

Purpose: Oligodendrocytes are cells responsible for myelination in the central nervous system and have been shown to undergo radiation‐induced apoptosis. The roles of ceramide and protein kinase B/Akt (PKB/Akt) were assessed in radiation‐induced apoptosis of oligodendrocytes in vitro.

Materials and methods: Primary cultures of oligodendrocytes were established from neonatal rat brains and cell identity was assessed by immunohistochemistry. Apoptosis was assessed histologically according to its specific morphologic features using 4′,6‐diaminido‐2‐phenylindole, and by transferase‐mediated deoxynucleotidyl transferase nick end‐labelling staining. The ceramide level was measured using a diacyglycerol kinase assay, and PKB/Akt activity was determined using immunoblotting and a protein kinase assay.

Results: Ionizing radiation, C2‐ceramide or wortmannin induced apoptosis in oligodendrocytes but not astrocytes. A rapid increase in ceramide was observed in oligodendrocytes after ionizing radiation. Monensin, an inhibitor of acid sphingomyelinase, reduced the apoptotic response in oligodendrocytes after ionizing radiation. Fumonisin B1, an inhibitor of ceramide synthase, showed no such effect in the cells. Radiation‐induced apoptosis of oligodendrocytes was associated with a decrease in PKB activity, similar to that observed after treatment with C2‐ceramide or wortmannin, but not after dihydro‐C2‐ceramide. Confocal microscopy revealed a loss of phosphorylated PKB immunostaining in the nucleus of apoptotic oligodendrocytes after ionizing radiation or C2‐ceramide treatment. The level of phosphorylated FKHRL1, a transcription factor phosphorylated by PKB, decreased in irradiated oligodendrocytes.

Conclusions: A ceramide–PKB‐mediated signalling pathway might play a role in radiation‐induced apoptosis of oligodendrocytes.