Hill Evan S, Vasireddi Sunil K, Wang Jean, Bruno Angela M, Frost William N
Department of Cell Biology and Anatomy, The Chicago Medical School, Rosalind Franklin University of Medicine and Science, 3333 Green Bay Road, North Chicago, IL 60064, USA.
Department of Cell Biology and Anatomy, The Chicago Medical School, Rosalind Franklin University of Medicine and Science, 3333 Green Bay Road, North Chicago, IL 60064, USA.
Curr Biol. 2015 Nov 16;25(22):2879-88. doi: 10.1016/j.cub.2015.09.033. Epub 2015 Nov 5.
Prior studies have found that functional networks can rapidly add neurons as they build short-term memories, yet little is known about the principles underlying this process. Using voltage-sensitive dye imaging, we found that short-term sensitization of Tritonia's swim motor program involves rapid expansion of the number of participating neurons. Tracking neurons across trials revealed that this involves the conversion of recently discovered variably participating neurons to reliable status. Further, we identify a candidate serotonergic cellular mechanism mediating this process. Our findings reveal a new mechanism for memory formation, involving recruitment of pre-positioned, variably committed neurons into memory networks. This represents a shift from the field's long-term focus on synaptic plasticity, toward a view that certain neurons have characteristics that predispose them to join networks with learning.
先前的研究发现,功能网络在构建短期记忆时能够迅速增加神经元,但对于这一过程背后的原理却知之甚少。利用电压敏感染料成像技术,我们发现海兔游泳运动程序的短期敏感化涉及参与神经元数量的快速增加。通过追踪不同实验中的神经元,我们发现这一过程涉及将最近发现的可变参与神经元转变为可靠状态。此外,我们确定了一种介导这一过程的候选血清素能细胞机制。我们的研究结果揭示了一种新的记忆形成机制,即招募预先定位的、可变参与的神经元进入记忆网络。这代表了该领域从长期关注突触可塑性,转向认为某些神经元具有使其倾向于通过学习加入网络的特征的观点转变。