Abrahamsson Therése, Gustafsson Bengt, Hanse Eric
University of Gothenburg, Department of Physiology, Box 432, Medicinaregatan 11, 405 30 Gothenburg, Sweden.
J Neurophysiol. 2008 Nov;100(5):2605-14. doi: 10.1152/jn.90476.2008. Epub 2008 Sep 17.
AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid) unsilencing is an often proposed expression mechanism both for developmental long-term potentiation (LTP), involved in circuitry refinement during brain development, and for mature LTP, involved in learning and memory. In the hippocampal CA3-CA1 connection naïve (nonstimulated) synapses are AMPA signaling and AMPA-silent synapses are created from naïve AMPA-signaling (AMPA-labile) synapses by test-pulse synaptic activation (AMPA silencing). To investigate to what extent LTPs at different developmental stages are explained by AMPA unsilencing, the amount of LTP obtained at these different developmental stages was related to the amount of AMPA silencing that preceded the induction of LTP. When examined in the second postnatal week Hebbian induction was found to produce no more stable potentiation than that causing a return to the naïve synaptic strength existing prior to the AMPA silencing. Moreover, in the absence of a preceding AMPA silencing Hebbian induction produced no stable potentiation above the naïve synaptic strength. Thus this early, or developmental, LTP is nothing more than an unsilencing (dedepression) and stabilization of the AMPA signaling that was lost by the prior AMPA silencing. This dedepression and stabilization of AMPA signaling was mimicked by the presence of the protein kinase A activator forskolin. As the relative degree of AMPA silencing decreased with development, LTP manifested itself more and more as a "genuine" potentiation (as opposed to a dedepression) not explained by unsilencing and stabilization of AMPA-labile synapses. This "genuine," or mature, LTP rose from close to nothing of total LTP prior to postnatal day (P)13, to about 70% of total LTP at P16, and to about 90% of total LTP at P30. Developmental LTP, by stabilization of AMPA-labile synapses, thus seems adapted to select synaptic connections to the growing synaptic network. Mature LTP, by instead strengthening existing stable connections between cells, may then create functionally tightly connected cell assemblies within this network.
α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)沉默解除是一种常被提出的表达机制,既适用于发育性长时程增强(LTP),其参与大脑发育过程中的神经回路精细化,也适用于成熟LTP,其参与学习和记忆。在海马CA3-CA1连接中,未成熟(未受刺激)的突触是AMPA信号传导的,而AMPA沉默突触是由未成熟的AMPA信号传导(AMPA不稳定)突触通过测试脉冲突触激活(AMPA沉默)产生的。为了研究在不同发育阶段的LTP在多大程度上可由AMPA沉默解除来解释,在这些不同发育阶段获得的LTP量与LTP诱导之前的AMPA沉默量相关。在出生后第二周进行检查时,发现赫布型诱导产生的增强并不比导致恢复到AMPA沉默之前存在的未成熟突触强度更稳定。此外,在没有先前的AMPA沉默的情况下,赫布型诱导不会产生高于未成熟突触强度的稳定增强。因此,这种早期的或发育性的LTP只不过是对先前AMPA沉默所丧失的AMPA信号传导的沉默解除(去抑制)和稳定化。蛋白激酶A激活剂福斯可林的存在模拟了AMPA信号传导的这种去抑制和稳定化。随着AMPA沉默的相对程度随着发育而降低,LTP越来越多地表现为一种“真正的”增强(与去抑制相反),这无法由AMPA不稳定突触的沉默解除和稳定化来解释。这种“真正的”或成熟的LTP从出生后第13天之前几乎占总LTP的零,上升到出生后第16天占总LTP的约70%,以及出生后第30天占总LTP的约90%。因此,发育性LTP通过稳定AMPA不稳定突触,似乎适合于选择与不断生长的突触网络的突触连接。相反,成熟LTP通过加强细胞之间现有的稳定连接,可能会在这个网络内创建功能紧密连接的细胞集合体。