Department of Pharmacology, Emory University School of Medicine, Rollins Research Center, Atlanta, GA 30322, USA.
Trends Pharmacol Sci. 2011 Nov;32(11):666-74. doi: 10.1016/j.tips.2011.07.005. Epub 2011 Sep 8.
Learning and memory are encoded within the brain as biochemical and physical changes at synapses that alter synaptic transmission, a process known as synaptic plasticity. Although much is known about factors that positively regulate synaptic plasticity, very little is known about factors that negatively regulate this process. Recently, the signaling protein RGS14 (Regulator of G protein Signaling 14) was identified as a natural suppressor of hippocampal-based learning and memory as well as synaptic plasticity within CA2 hippocampal neurons. RGS14 is a multifunctional scaffolding protein that integrates unconventional G protein and mitogen-activated protein (MAP) kinase signaling pathways that are themselves key regulators of synaptic plasticity, learning, and memory. Here, we highlight the known roles for RGS14 in brain physiology and unconventional G protein signaling pathways, and propose molecular models to describe how RGS14 may integrate these diverse signaling pathways to modulate synaptic plasticity in CA2 hippocampal neurons.
学习和记忆是在突触中作为生化和物理变化来编码的,这些变化改变了突触传递,这一过程被称为突触可塑性。虽然人们已经了解了很多正向调节突触可塑性的因素,但对于负向调节这一过程的因素却知之甚少。最近,信号蛋白 RGS14(G 蛋白信号调节因子 14)被确定为海马相关学习和记忆以及 CA2 海马神经元中突触可塑性的天然抑制剂。RGS14 是一种多功能支架蛋白,可整合非传统的 G 蛋白和丝裂原活化蛋白激酶(MAP)激酶信号通路,而这些信号通路本身就是突触可塑性、学习和记忆的关键调节因子。在这里,我们强调了 RGS14 在大脑生理学和非传统 G 蛋白信号通路中的已知作用,并提出了分子模型来描述 RGS14 如何整合这些不同的信号通路来调节 CA2 海马神经元中的突触可塑性。