Department of Physiology and Biophysics, University of Washington, Seattle, Washington 98195, USA.
J Neurosci. 2011 Jun 29;31(26):9466-71. doi: 10.1523/JNEUROSCI.6311-10.2011.
Wnt ligands are secreted glycoproteins controlling gene expression and cytoskeleton reorganization involved in embryonic development of the nervous system. However, their role in later stages of brain development, particularly in the regulation of established synaptic connections, is not known. We found that Wnt-5a acutely and specifically upregulates synaptic NMDAR currents in rat hippocampal slices, facilitating induction of long-term potentiation, a cellular model of learning and memory. This effect requires an increase in postsynaptic Ca(2+) and activation of noncanonical downstream effectors of the Wnt signaling pathway. In contrast, Wnt-7a, an activator of the canonical Wnt signaling pathway, has no effect on NMDAR-mediated synaptic transmission. Moreover, endogenous Wnt ligands are necessary to maintain basal NMDAR synaptic transmission, adjusting the threshold for synaptic potentiation. This novel role for Wnt ligands provides a mechanism for Wnt signaling to acutely modulate synaptic plasticity and brain function in later stages of development and in the mature organism.
Wnt 配体是分泌的糖蛋白,可控制基因表达和细胞骨架重组,参与神经系统的胚胎发育。然而,它们在大脑发育的后期阶段,特别是在调节已建立的突触连接中的作用尚不清楚。我们发现 Wnt-5a 可在大鼠海马切片中急性且特异性地上调突触 NMDA 受体电流,促进长时程增强(学习和记忆的细胞模型)的诱导。这种作用需要增加突触后 Ca2+并激活 Wnt 信号通路的非经典下游效应物。相比之下,Wnt-7a(经典 Wnt 信号通路的激活剂)对 NMDA 介导的突触传递没有影响。此外,内源性 Wnt 配体对于维持基础 NMDA 突触传递是必需的,从而调整了突触增强的阈值。Wnt 配体的这种新作用为 Wnt 信号提供了一种机制,可在发育后期和成熟生物体中急性调节突触可塑性和大脑功能。