Ancatén-González Carlos, Meza Rodrigo C, Gonzalez-Sanabria Naileth, Segura Ignacio, Alcaino Alejandro, Peña-Pichicoi Antonio, Latorre Ramón, Chiu Chiayu Q, Chávez Andrés E
Programa de Doctorado en Ciencias Mención Neurociencia, Facultad de Ciencias, Universidad de Valparaíso, Valparaíso 2340000, Chile.
Instituto de Neurociencias, Centro Interdisciplinario de Neurociencia de Valparaíso, Facultad de Ciencias, Universidad de Valparaíso, Valparaíso 2340000, Chile.
Proc Natl Acad Sci U S A. 2025 Jan 14;122(2):e2411506122. doi: 10.1073/pnas.2411506122. Epub 2025 Jan 8.
BK channels can control neuronal function, but their functional relevance in activity-dependent changes of synaptic function remains elusive. Here, we report that repetitive low-frequency stimulation activates BK channels through 12(S)HPETE, an arachidonic acid metabolite, produced downstream of postsynaptic metabotropic glutamate receptors (mGluRs) to trigger long-term depression (LTD) at CA3-CA1 synapses in hippocampal slices from P7-P10 mice. Activation of BK channels is subunit specific, as paxilline but not iberiotoxin blocked mGluR-LTD. Also, 12(S)HPETE does not change the electrophysiological properties of the BK channel when the BKα subunit is expressed alone but increases the channel open probability when the BKα is coexpressed with the β4-subunit. Our findings reveal an interaction between 12(S)HPETE and BK channels to regulate synaptic strength at central synapses and increase our understanding of the mechanisms underlying mGluR-LTD in the neonatal hippocampus that likely contribute to circuit maturation necessary for learning.
BK通道可控制神经元功能,但其在突触功能的活动依赖性变化中的功能相关性仍不清楚。在此,我们报告重复低频刺激通过12(S)HPETE激活BK通道,12(S)HPETE是一种花生四烯酸代谢产物,在突触后代谢型谷氨酸受体(mGluRs)下游产生,以触发P7 - P10小鼠海马切片中CA3 - CA1突触处的长时程抑制(LTD)。BK通道的激活具有亚基特异性,因为蜂毒明肽而非iberiotoxin可阻断mGluR - LTD。此外,当单独表达BKα亚基时,12(S)HPETE不会改变BK通道的电生理特性,但当BKα与β4亚基共表达时,会增加通道开放概率。我们的研究结果揭示了12(S)HPETE与BK通道之间的相互作用,以调节中枢突触的突触强度,并增进了我们对新生海马体中mGluR - LTD潜在机制的理解,这可能有助于学习所需的神经回路成熟。