Misonou Hiroaki, Menegola Milena, Mohapatra Durga P, Guy Lauren K, Park Kang-Sik, Trimmer James S
Department of Pharmacology, School of Medicine, University of California, Davis, California 95616, USA.
J Neurosci. 2006 Dec 27;26(52):13505-14. doi: 10.1523/JNEUROSCI.3970-06.2006.
Activity-dependent dephosphorylation of neuronal Kv2.1 channels yields hyperpolarizing shifts in their voltage-dependent activation and homoeostatic suppression of neuronal excitability. We recently identified 16 phosphorylation sites that modulate Kv2.1 function. Here, we show that in mammalian neurons, compared with other regulated sites, such as serine (S)563, phosphorylation at S603 is supersensitive to calcineurin-mediated dephosphorylation in response to kainate-induced seizures in vivo, and brief glutamate stimulation of cultured hippocampal neurons. In vitro calcineurin digestion shows that supersensitivity of S603 dephosphorylation is an inherent property of Kv2.1. Conversely, suppression of neuronal activity by anesthetic in vivo causes hyperphosphorylation at S603 but not S563. Distinct regulation of individual phosphorylation sites allows for graded and bidirectional homeostatic regulation of Kv2.1 function. S603 phosphorylation represents a sensitive bidirectional biosensor of neuronal activity.
神经元Kv2.1通道的活性依赖性去磷酸化使其电压依赖性激活产生超极化偏移,并对神经元兴奋性进行稳态抑制。我们最近鉴定出16个调节Kv2.1功能的磷酸化位点。在此,我们表明,在哺乳动物神经元中,与其他受调节位点(如丝氨酸(S)563)相比,S603位点的磷酸化对体内海藻酸盐诱导的癫痫发作以及培养的海马神经元的短暂谷氨酸刺激所引起的钙调神经磷酸酶介导的去磷酸化超敏感。体外钙调神经磷酸酶消化显示,S603去磷酸化的超敏感性是Kv2.1的固有特性。相反,体内麻醉剂对神经元活动的抑制会导致S603而非S563的过度磷酸化。各个磷酸化位点的不同调节允许对Kv2.1功能进行分级和双向的稳态调节。S603磷酸化代表了一种敏感的神经元活动双向生物传感器。