1] State Key Laboratory of Organ Failure Research, Department of Neurobiology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China. [2] Key Laboratory of Neuroplasticity of Guangdong Higher Education Institutes, Southern Medical University, Guangzhou, China.
School of Public Health and Tropical Medicine, Southern Medical University, Guangzhou, China.
Nat Neurosci. 2014 Aug;17(8):1055-63. doi: 10.1038/nn.3744. Epub 2014 Jun 22.
Ion channels are essential for the regulation of neuronal functions. The significance of plasma membrane, mitochondrial, endoplasmic reticulum and lysosomal ion channels in the regulation of Ca(2+) is well established. In contrast, surprisingly little is known about the function of ion channels on the nuclear envelope (NE). Here we demonstrate the presence of functional large-conductance, calcium-activated potassium channels (BK channels) on the NE of rodent hippocampal neurons. Functionally, blockade of nuclear BK channels (nBK channels) induces NE-derived Ca(2+) release, nucleoplasmic Ca(2+) elevation and cyclic AMP response element binding protein (CREB)-dependent transcription. More importantly, blockade of nBK channels regulates nuclear Ca(2+)-sensitive gene expression and promotes dendritic arborization in a nuclear Ca(2+)-dependent manner. These results suggest that the nBK channel functions as a molecular link between neuronal activity and nuclear Ca(2+) to convey signals from synapse to nucleus and is a new modulator, operating at the NE, of synaptic activity-dependent neuronal functions.
离子通道对于神经元功能的调节至关重要。已经证实,质膜、线粒体、内质网和溶酶体离子通道在调节 Ca(2+)方面具有重要意义。相比之下,关于核膜(NE)上离子通道的功能却知之甚少。本文作者证明了啮齿动物海马神经元 NE 上存在功能性大电导、钙激活钾通道(BK 通道)。功能上,核 BK 通道(nBK 通道)的阻断会诱导 NE 源性 Ca(2+)释放、核质 Ca(2+)升高和环磷酸腺苷反应元件结合蛋白(CREB)依赖性转录。更重要的是,nBK 通道的阻断以核 Ca(2+)依赖的方式调节核 Ca(2+)敏感基因表达并促进树突分支。这些结果表明,nBK 通道作为神经元活动和核 Ca(2+)之间的分子联系,将信号从突触传递到核,并作为一种新的调节剂,在 NE 上调节突触活动依赖性神经元功能。