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DOI 10.1021/acschemneuro.6b00222

Медицинская библиотека · ACS chemical neuroscience · 2016

miRNA-187-3p-Mediated Regulation of the KCNK10/TREK-2 Potassium Channel in a Rat Epilepsy Model.

Haenisch Sierk, von Rüden Eva-Lotta, Wahmkow Hannes, Rettenbeck Maruja L, Michler Christina, Russmann Vera, Bruckmueller Henrike, Waetzig Vicki, Cascorbi Ingolf, Potschka Heidrun

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Аннотация

Regulatory RNAs play a key role in the regulation of protein expression patterns in neurological diseases. Here we studied the regulation of miRNAs in a chronic rat model of temporal lobe epilepsy. The analysis was focused on a putative link with pharmacoresponsiveness as well as the functional implications of the regulation of a selected miRNA. The findings did not reveal a difference in hippocampal miRNA expression between phenobarbital responders and nonresponders. However, when comparing rats following status epilepticus with control rats we identified 13 differentially expressed miRNAs with miRNA-187-3p being most strongly regulated. mRNAs encoding KCNK10/TREK-2 as well as DYRK2 were confirmed as targets of miRNA-187-3p. Expression of the potassium channel protein KCNK10/TREK-2 negatively correlated with hippocampal miRNA-187-3p expression and proved to be upregulated in the chronic phase of the epilepsy model. In conclusion, our data do not suggest a relevant impact of miRNA expression patterns on pharmacoresponsiveness. However, we confirmed regulation of miRNA-187-3p and demonstrated that it impacts the expression of the two-pore domain potassium channel protein KCNK10/TREK-2. Considering evidence from brain ischemia models, KCNK10/TREK-2 upregulation might serve a protective function with a beneficial impact on astrocytic potassium and glutamate homeostasis.

Для цитирования: Haenisch Sierk, von Rüden Eva-Lotta, Wahmkow Hannes, Rettenbeck Maruja L, Michler Christina, Russmann Vera, Bruckmueller Henrike, Waetzig Vicki, Cascorbi Ingolf, Potschka Heidrun. miRNA-187-3p-Mediated Regulation of the KCNK10/TREK-2 Potassium Channel in a Rat Epilepsy Model.. ACS chemical neuroscience. 2016. DOI: 10.1021/acschemneuro.6b00222.

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