Amphotericin B–Induced Interleukin‐1β Expression in Human Monocytic Cells is Calcium and Calmodulin Dependent

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Abstract
Amphotericin B remains the agent of choice for treatment of severe fungal infections. Its use is hindered by adverse effects, including infusion-related fever, chills, and hypotension, as well as nephrotoxicity with secondary anemia, hypokalemia, and hypomagnesemia. Amphotericin B-induced transcription and expression of interleukin (IL)-lβ by human monocytes is believed to be involved in mediating infusion-related adverse effects. It is shown here that agents that increase intracellular calcium [Ca++], (A23187 and thapsigargin) in human monocytic cells also induce IL-1ß expression. Furthermore, amphotericin B-induced IL-lβ expression is attenuated by the calmodulin antagonist calmidazolium. Amphotericin B 5.41 μM increases [Ca++], by up to 300 nM in these cells. In the presence of a nominal calcium buffer or EGTA, amphotericin B-induced IL-1γ expression is attenuated. Thus, amphotericin B acts as an ionophore to increase [Ca++], and activates calmodulin-mediated expression of IL-lγ in human monocytes.

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