Abstract

Cerebral tissue acidosis following ischemia or traumatic brain injury contributes to cytotoxic brain edema formation. In vitro lactacidosis induces swelling of glial cells by intracellular Na +- and Cl −-accumulation by the Na +/H +-antiporter, Cl −/HCO 3 −-antiporters and the Na +–K +–2Cl −-cotransport. The present study aimed to elucidate whether mechanisms of lactacidosis-induced glial swelling are dependent on intra- or extracellular Ca 2+-ions. Therefore, C6 glioma cells were exposed to a lactacidosis of pH 6.2 in standard or calcium-free medium and following intracellular calcium chelation. Cell volume and intracellular pH were assessed by flow cytometry. Lactacidosis of pH 6.2 induced a prompt and sustained swelling of suspended C6 glioma cells reaching a maximum of 128% within 60 min. Omission of Ca 2+ from the suspension medium strongly attenuated cell swelling while chelation of intracellular Ca 2+ had no effects. Intracellular acidosis was not affected by either treatment. The present data show a strong dependency of lactacidosis-induced glial swelling upon extracellular Ca 2+ while intracellular acidosis is not affected by omission of [Ca 2+] e. Therefore, our data suggest that the Na +–K +–2Cl −-cotransporter, the only so far known transporter involved in cell volume regulation but not in pH i regulation during lactacidosis, is activated in a [Ca 2+] e-dependent manner.

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