AUTHOR=Foncelle Alexandre , Mendes Alexandre , Jędrzejewska-Szmek Joanna , Valtcheva Silvana , Berry Hugues , Blackwell Kim T. , Venance Laurent TITLE=Modulation of Spike-Timing Dependent Plasticity: Towards the Inclusion of a Third Factor in Computational Models JOURNAL=Frontiers in Computational Neuroscience VOLUME=12 YEAR=2018 URL=https://www.frontiersin.org/journals/computational-neuroscience/articles/10.3389/fncom.2018.00049 DOI=10.3389/fncom.2018.00049 ISSN=1662-5188 ABSTRACT=
In spike-timing dependent plasticity (STDP) change in synaptic strength depends on the timing of pre- vs. postsynaptic spiking activity. Since STDP is in compliance with Hebb’s postulate, it is considered one of the major mechanisms of memory storage and recall. STDP comprises a system of two coincidence detectors with N-methyl-D-aspartate receptor (NMDAR) activation often posited as one of the main components. Numerous studies have unveiled a third component of this coincidence detection system, namely neuromodulation and glia activity shaping STDP. Even though dopaminergic control of STDP has most often been reported, acetylcholine, noradrenaline, nitric oxide (NO), brain-derived neurotrophic factor (BDNF) or gamma-aminobutyric acid (GABA) also has been shown to effectively modulate STDP. Furthermore, it has been demonstrated that astrocytes, via the release or uptake of glutamate, gate STDP expression. At the most fundamental level, the timing properties of STDP are expected to depend on the spatiotemporal dynamics of the underlying signaling pathways. However in most cases, due to technical limitations experiments grant only indirect access to these pathways. Computational models carefully constrained by experiments, allow for a better qualitative understanding of the molecular basis of STDP and its regulation by neuromodulators. Recently, computational models of calcium dynamics and signaling pathway molecules have started to explore STDP emergence in