Chergui Karima, Svenningsson Per, Greengard Paul
Laboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York 10021, USA.
J Neurosci. 2005 Jul 13;25(28):6601-9. doi: 10.1523/JNEUROSCI.1082-05.2005.
Casein kinase 1 (CK1) is a highly conserved serine/threonine kinase, present in virtually all cell types, in which it phosphorylates a wide variety of substrates. So far, no role has been found for this ubiquitous protein kinase in the physiology of nerve cells. In the present study, we show that CK1 regulates fast synaptic transmission mediated by glutamate, the major excitatory neurotransmitter in the brain. Through the use of CK1 inhibitors, we present evidence that activation of CK1 decreases NMDA receptor activity in the striatum via a mechanism that involves activation by this kinase of protein phosphatase 1 and/or 2A and resultant increased dephosphorylation of NMDA receptors. Indeed, inhibition of CK1 increases NMDA-mediated EPSCs in medium spiny striatal neurons. This effect is associated with an increased phosphorylation of the NR1 and NR2B subunits of the NMDA receptor and is occluded by the phosphatase inhibitor okadaic acid. The mGluR1, but not mGluR5, subclass of metabotropic glutamate receptors uses CK1 to inhibit NMDA-mediated synaptic currents. These results provide the first evidence for a role of CK1 in the regulation of synaptic transmission in the brain.
酪蛋白激酶1(CK1)是一种高度保守的丝氨酸/苏氨酸激酶,几乎存在于所有细胞类型中,可磷酸化多种底物。到目前为止,尚未发现这种普遍存在的蛋白激酶在神经细胞生理学中有任何作用。在本研究中,我们表明CK1调节由谷氨酸介导的快速突触传递,谷氨酸是大脑中的主要兴奋性神经递质。通过使用CK1抑制剂,我们提供证据表明,CK1的激活通过一种机制降低纹状体中NMDA受体的活性,该机制涉及该激酶对蛋白磷酸酶1和/或2A的激活以及由此导致的NMDA受体去磷酸化增加。事实上,抑制CK1会增加中等棘状纹状体神经元中NMDA介导的兴奋性突触后电流(EPSCs)。这种效应与NMDA受体的NR1和NR2B亚基磷酸化增加有关,并且被磷酸酶抑制剂冈田酸所阻断。代谢型谷氨酸受体的mGluR1亚型而非mGluR5亚型利用CK1来抑制NMDA介导的突触电流。这些结果为CK1在调节大脑突触传递中的作用提供了首个证据。