Organ-specific manganese toxicity: a comparative in vitro study on five cellular models exposed to MnCl2.

Manganese (Mn) is both an essential nutrient and a toxicant, with speciWc eVects on liver and kidney (acute exposure) and on central nervous system (CNS) (chronic exposure). Mn neurotoxicity includes neurobehavioral disorders and extra-pyramidal motor dysfunctions (manganism), possibly due to focal injuries to the basal ganglia. Even if widely investigated, the molecular mechanisms responsible for Mn toxicity remain to be clariWed. Aim of this study was to identify suitable in vitro models to investigate these molecular pathways. To this purpose we compared the eVect of manganese chloride on four cell lines, representative of the main target organs of Mn toxicity in vivo. HepG2 and MDCK cell lines were selected for liver and kidney, respectively; glial GL15 and neuronal SHSY5Y cells were used as models of CNS components. To complete the “motor system” model, skeletal muscle C2C12 cells were also included. Our results demonstrate that hepatic, renal, glial and neuronal cell types diVerently react to Mn, mirroring the speciWc in vivo response of the tissue they represent. This conWrms their value as suitable in vitro models to study Mn-related toxic events. Interestingly, also muscle C2C12 cells showed a noticeable sensitivity to Mn, preferential targets being diVerentiated myotubes.