IGF/mTORC1/S6 Signaling Is Potentiated and Prolonged by Acute Loading of Subtoxicological Manganese Ion.

The insulin-like growth factor (IGF)/insulin signaling (IIS) pathway is involved in cellular responses against intracellular divalent manganese ion (Mn 2+ ) accumulation. As a pathway where multiple nodes utilize Mn 2+ as a metallic co-factor, how the IIS signaling patterns are affected by Mn 2+ overload is unresolved. In our prior studies, acute Mn 2+ exposure potentiated IIS kinase activity upon physiological-level stimulation, indicated by elevated phosphorylation of protein kinase B (PKB, also known as AKT). AKT phosphorylation is associated with IIS activity; and provides direct signaling transduction input for the mammalian target of rapamycin complex 1 (mTORC1) and its downstream target ribosomal protein S6 (S6). Here, to better define the impact of Mn 2+ exposure on IIS function, Mn 2+ -induced IIS activation was evaluated with serial concentrations and temporal endpoints. In the wild-type murine striatal neuronal line ST Hdh , the acute treatment of Mn 2+ with IGF induced a Mn 2+ concentration-sensitive phosphorylation of S6 at Ser235/236 to as low as 5 μM extracellular Mn 2+ . This effect required both the essential amino acids and insulin receptor (IR)/IGF receptor (IGFR) signaling input. Similar to simultaneous stimulation of Mn 2+ and IGF, when a steady-state elevation of Mn 2+ was established via a 24-h pre-exposure, phosphorylation of S6 also displayed higher sensitivity to sub-cytotoxic Mn 2+ when compared to AKT phosphorylation at Ser473. This indicates a synergistic effect of sub-cytotoxic Mn 2+ on IIS and mTORC1 signaling. Furthermore, elevated intracellular Mn 2+ , with both durations, led to a prolonged activation in AKT and S6 upon stimulation. Our data demonstrate that the downstream regulator S6 is a highly sensitive target of elevated Mn 2+ and is well below the established acute cytotoxicity thresholds (<50 μM). These findings indicate that the IIS/mTORC1 pathways, in which Mn 2+ normally serves as an essential co-factor, are dually responsible for the cellular changes in exposures to real-world Mn 2+ concentrations.