基于Ca2+/钙调素依赖性蛋白激酶特性的长期记忆模型的评估。

Journal de physiologie Pub Date : 1988-01-01
J Lisman, M Goldring
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引用次数: 0

摘要

1.) 本文进一步探讨了长期记忆模型的可行性(Lisman, 1985;Lisman and Goldring, 1988)。根据该模型,单个突触的突触效能值由突触后密度中包含的Ca2+/钙调素依赖性蛋白激酶II分子组局部存储。2)。在之前的一篇论文中提出的计算表明,这些激酶分子编码具有长期记忆所需的稳定性的信息是可行的。这些计算是基于酶上的30个磷酸化位点以串行方式磷酸化的假设,即这些位点不是独立的。本文提出了类似的计算基于另一种假设,即位点是独立磷酸化的。3.) 被“打开”的激酶分子经历了一个连续的去磷酸化和再磷酸化过程。对这个循环所消耗的能量的估计表明,所需的能量不会对神经元代谢产生不合理的要求。讨论了分子开关耗能的必要性。4)。Ca2+/钙调蛋白依赖激酶的分子内自磷酸化速率表明,胞质游离Ca2+浓度必须保持升高几秒钟,才能使激酶分子“打开”。讨论了如何实现Ca2+的持续上升。5)。另一种观点认为,长期记忆的储存与基因表达的变化有关。支持这一观点的主要证据是蛋白质合成抑制剂对记忆的影响。一个模型显示,观察到的蛋白质合成抑制剂的作用并不一定意味着信息存储是在基因表达水平。6)。“突触前”和“突触后”联想学习机制之间的区别进行了讨论。结论是,这种区别可能具有误导性,不应排除潜在机制相似的可能性。
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Evaluation of a model of long-term memory based on the properties of the Ca2+/calmodulin-dependent protein kinase.

1.) This paper further explores the feasibility of a model for long-term memory (Lisman, 1985; Lisman and Goldring, 1988). According to this model, the value of synaptic efficacy of individual synapses is stored locally by the group of Ca2+/calmodulin-dependent protein kinase II molecules contained within the post-synaptic density. 2.) Calculations presented in a previous paper indicate that it is feasible for these kinase molecules to encode information with the stability required for long-term memory. These calculations were based on the assumption that the 30 phosphorylation sites on the enzyme are phosphorylated in a serial fashion, i.e. that the sites are not independent. This paper presents similar calculations based on the alternative assumption that the sites are phosphorylated independently. 3.) Kinase molecules that have been switched "on" undergo a continuous process of dephosphorylation and rephosphorylation. Estimates of the energy consumed by this cycle indicate that the energy required would not make unreasonable demands on neuronal metabolism. The necessity of energy consumption by molecular switches is discussed. 4.) The rate of intramolecular autophosphorylation of the Ca2+/calmodulin dependent kinase implies that the cytoplasmic free Ca2+ concentration must stay elevated for several seconds in order for kinase molecules to switch "on". How such a sustained rise in Ca2+ might be achieved is discussed. 5.) An alternative view is that long-term memory storage involves a change in gene expression. The principal evidence supporting this view is the effect of protein synthesis inhibitors on memory. A model is presented showing that the observed effect of protein synthesis inhibitors does not necessarily imply that information storage is at the level of gene expression. 6.) The distinction between "presynaptic" and "postsynaptic" associative learning mechanisms is discussed. It is concluded that this distinction can be misleading and that the possibility that the underlying mechanisms are similar should not be excluded.

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