Bayazitov Ildar T, Richardson Robert J, Fricke Robert G, Zakharenko Stanislav S
Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.
J Neurosci. 2007 Oct 24;27(43):11510-21. doi: 10.1523/JNEUROSCI.3077-07.2007.
Long-term potentiation (LTP) mediates learning and memory in the mammalian hippocampus. Whether a presynaptic or postsynaptic neuron principally enhances synaptic transmission during LTP remains controversial. Acute hippocampal slices were made from transgenic mouse strains that express synaptopHluorin in neurons. SynaptopHluorin is an indicator of synaptic vesicle recycling; thus, we monitored functional changes in presynaptic boutons of CA3 pyramidal cells by measuring changes in synaptopHluorin fluorescence. Simultaneously, we recorded field excitatory postsynaptic potentials to monitor changes in the strength of excitatory synapses between CA3 and CA1 pyramidal neurons. We found that LTP consists of two components, a slow presynaptic component and a fast postsynaptic component. The presynaptic mechanisms contribute mostly to the late phase of compound LTP, whereas the postsynaptic mechanisms are crucial during the early phase of LTP. We also found that protein kinase A (PKA) and L-type voltage-gated calcium channels are crucial for the expression of the presynaptic component of compound LTP, and NMDA channels are essential for that of the postsynaptic component of LTP. These data are the first direct evidence that presynaptic and postsynaptic components of LTP are temporally and mechanistically distinct.
长时程增强(LTP)介导哺乳动物海马体中的学习和记忆。在LTP过程中,究竟是突触前神经元还是突触后神经元主要增强突触传递仍存在争议。从在神经元中表达突触pH荧光蛋白的转基因小鼠品系制备急性海马切片。突触pH荧光蛋白是突触小泡循环的一个指标;因此,我们通过测量突触pH荧光蛋白荧光的变化来监测CA3锥体细胞突触前终扣的功能变化。同时,我们记录场兴奋性突触后电位,以监测CA3和CA1锥体细胞之间兴奋性突触强度的变化。我们发现LTP由两个成分组成,一个缓慢的突触前成分和一个快速的突触后成分。突触前机制主要作用于复合LTP的后期,而突触后机制在LTP的早期至关重要。我们还发现蛋白激酶A(PKA)和L型电压门控钙通道对复合LTP突触前成分的表达至关重要,而NMDA通道对LTP突触后成分的表达必不可少。这些数据是LTP的突触前和突触后成分在时间和机制上截然不同的首个直接证据。