The effects of Cuprizone on murine subventricular zone-derived neural stem cells and progenitor cells grown as neurospheres

MOLINARI YAMILA A.; BYRNE AGUSTÍN JESÚS; PEREZ MARIA JULIA; SILVESTROFF LUCAS; FRANCO PAULA G.

MOLECULAR NEUROBIOLOGY

HUMANA PRESS INC

Lugar: Totowa, NJ; Año: 2022

0893-7648

Despite the extensive use of the cuprizone (CPZ) demyelination animal model, there is little evidence regarding the effects of CPZ on a cellular level. Initial studies have suggested that oligodendrocytes (OL) are the main cell targets for CPZ toxicity. However, recent data have revealed additional effects on neural stem cells and progenitor cells (NSC/NPC), which constitute a reservoir for OL regeneration during brain remyelination.We cultured NSC/NPC as neurospheres to investigate CPZ effects on cell mechanisms which are thought to be involved in demyelination and remyelination processes in vivo. Proliferating NSC/NPC cultures exposed to CPZ showed overproduction of intracellular reactive oxygen species and increased progenitor migration at the expense of a significant inhibition of cell proliferation. Although NSC/NPC survival was not affected by CPZ in proliferative conditions, we found that CPZ treated cultures undergoing cell differentiation were more prone to cell death than controls. The commitment and cell differentiation towards neural lineages did not seem to be affected by CPZ, as shown by the conserved proportions of OL, astrocytes and neurons. Nevertheless, when CPZ treatment was performed after cell differentiation, we detected a significant reduction in the number and the morphological complexity of OL, astrogliosis and neuronal damage. We conclude that, in addition to damaging mature OL, CPZ also reduces NSC/NPC proliferation and activates progenitor migration. These results shed light on CPZ toxicity in the brain and could serve to understand the exhaustion of regenerative mechanisms from NSC/NPC in the chronic CPZ animal model.