Abstract
The goal of this study was to evaluate an effect of interleukin-10 (IL-10) on the Ca2+ response induced by repeated NMDA receptor activation with brief hypoxia in cultured hippocampal neurons. We focused on the importance of internal Ca2+ stores in the modulation of this Ca2+ response by IL-10. To test this, we compared roles of InsP3- and ryanodine-sensitive internal stores in the effects of IL-10. Measurements of intracellular cytosolic calcium concentration ([Ca2+]i) in cultured hippocampal neurons were made by imaging Fura-2AM loaded hippocampal cells. Repeated episodes of NMDA receptor activation with brief hypoxia induced the spontaneous (s) [Ca2+]i increases about 3min after each hypoxic episode. The amplitude of the s[Ca2+]i increases was progressively enhanced from the first hypoxic episode to the third one. IL-10 (1ng/ml) abolished these s[Ca2+]i increases. Exposure of cultured hippocampal neurons with thapsigargin (1μM) or an inhibitor of phospholipase C (U73122, 1μM) for 10min also abolished the s[Ca2+]i increases. On the other hand, antagonist of ryanodine receptors (ryanodine, 1μM) did not affect this Ca2+ response. These studies appear to provide the first evidence that Ca2+ release from internal stores is affected by anti-inflammatory cytokine IL-10 in brain neurons. It is suggested that these data increase our understanding of the neuroprotective mechanisms of IL-10 in the early phase of hypoxia.
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