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Fine control of neuronal activity is crucial to rapidly adjust to subtle changes of the environment. This fine tuning was thought to be purely neuronal until the discovery that astrocytes are active players of synaptic transmission. In the adult hippocampus, microglia are the other major glial cell type. Microglia are highly dynamic and closely associated with neurons and astrocytes. They react rapidly to modifications of their environment and are able to release molecules known to control neuronal function and synaptic transmission. Therefore, microglia display functional features of synaptic partners, but their involvement in the regulation of synaptic transmission has not yet been addressed. We have used a combination of pharmacological approaches with electrophysiological analysis on acute hippocampal slices and ATP assays in purified cell cultures to show that activation of microglia induces a rapid increase of spontaneous excitatory postsynaptic currents. We found that this modulation is mediated by binding of ATP to P2Y1R located on astrocytes and is independent of TNFα or NOS2. Our data indicate that, on activation, microglia cells rapidly release small amounts of ATP, and astrocytes, in turn, amplified this release. Finally, P2Y1 stimulation of astrocytes increased excitatory postsynaptic current frequency through a metabotropic glutamate receptor 5-dependent mechanism. These results indicate that microglia are genuine regulators of neurotransmission and place microglia as upstream partners of astrocytes. Because pathological activation of microglia and alteration of neurotransmission are two early symptoms of most brain diseases, our work also provides a basis for understanding synaptic dysfunction in neuronal diseases.

Key Points In the CNS, the postsynaptic response to an action potential is variable: neurotransmitter release is probabilistic and the postsynaptic response to neurotransmitter release has variable timing and amplitude. Synaptic transmission results from a sequence of reactive and diffusive molecular processes (such as conformational changes, binding events and diffusion) that display stochastic properties at the molecular scale. At individual synapses, the number of molecules of a given type is small and the stochastic properties of molecular events cannot be neglected. These stochastic properties underlie the variability of the postsynaptic response evoked by an action potential. The stochasticity of presynaptic molecular processes affects the probability of vesicular release, and the stochasticity of postsynaptic molecular processes accounts for the variability in timing and amplitude of the evoked postsynaptic potential. The stochasticity of molecular events seems to be in contradiction with the reliability of synaptic transmission, which raises the issues of robustness and sensitivity in the process. Building an integrated view of how the stochasticity of molecular processes contributes to the variability of synaptic transmission but is nevertheless also compatible with a reliable transmission, is a challenge. A key element is that the steps of synaptic transmission are temporally coupled to each other in cascade. The characteristics of the coupling between steps are likely to reduce the propagation of fluctuations and/or enhance the sensitivity of the system (the ability to distinguish signal from random fluctuations). These characteristics probably include temporal organization of signalling, spatial organization of molecules, cooperativity and stochastic resonance. The number of individual types of molecules that are involved in synaptic transmission is small enough for the stochastic (random) properties of molecular events to be non-negligible. Triller and colleagues discuss the implications of stochastic reactive and diffusive molecular behaviours for synaptic transmission. The variability of the postsynaptic response following a single action potential arises from two sources: the neurotransmitter release is probabilistic, and the postsynaptic response to neurotransmitter release has variable timing and amplitude. At individual synapses, the number of molecules of a given type that are involved in these processes is small enough that the stochastic (random) properties of molecular events cannot be neglected. How the stochasticity of molecular processes contributes to the variability of synaptic transmission, its sensitivity and its robustness to molecular fluctuations has important implications for our understanding of the mechanistic basis of synaptic transmission and of synaptic plasticity.

This paper presents Yellow Fluorescence-Activating and absorption-Shifting Tag (Y-FAST), a small monomeric protein tag, half as large as the green fluorescent protein, enabling fluorescent labeling of proteins in a reversible and specific manner through the reversible binding and activation of a cell-permeant and nontoxic fluorogenic ligand (a so-called fluorogen). A unique fluorogen activation mechanism based on two spectroscopic changes, increase of fluorescence quantum yield and absorption red shift, provides high labeling selectivity. Y-FAST was engineered from the 14-kDa photoactive yellow protein by directed evolution using yeast display and fluorescence-activated cell sorting. Y-FAST is as bright as common fluorescent proteins, exhibits good photostability, and allows the efficient labeling of proteins in various organelles and hosts. Upon fluorogen binding, fluorescence appears instantaneously, allowing monitoring of rapid processes in near real time. Y-FAST distinguishes itself from other tagging systems because the fluorogen binding is highly dynamic and fully reversible, which enables rapid labeling and unlabeling of proteins by addition and withdrawal of the fluorogen, opening new exciting prospects for the development of multiplexing imaging protocols based on sequential labeling.

Precise quantitative information about the molecular architecture of synapses is essential to understanding the functional specificity and downstream signaling processes at specific populations of synapses. Glycine receptors (GlyRs) are the primary fast inhibitory neurotransmitter receptors in the spinal cord and brainstem. These inhibitory glycinergic networks crucially regulate motor and sensory processes. Thus far, the nanoscale organization of GlyRs underlying the different network specificities has not been defined. Here, we have quantitatively characterized the molecular arrangement and ultra-structure of glycinergic synapses in spinal cord tissue using quantitative super-resolution correlative light and electron microscopy. We show that endogenous GlyRs exhibit equal receptor-scaffold occupancy and constant packing densities of about 2000 GlyRs µm -2 at synapses across the spinal cord and throughout adulthood, even though ventral horn synapses have twice the total copy numbers, larger postsynaptic domains, and more convoluted morphologies than dorsal horn synapses. We demonstrate that this stereotypic molecular arrangement is maintained at glycinergic synapses in the oscillator mouse model of the neuromotor disease hyperekplexia despite a decrease in synapse size, indicating that the molecular organization of GlyRs is preserved in this hypomorph. We thus conclude that the morphology and size of inhibitory postsynaptic specializations rather than differences in GlyR packing determine the postsynaptic strength of glycinergic neurotransmission in motor and sensory spinal cord networks.

A growing number of long nuclear‐retained non‐coding RNAs (ncRNAs) have recently been described. However, few functions have been elucidated for these ncRNAs. Here, we have characterized the function of one such ncRNA, identified as metastasis‐associated lung adenocarcinoma transcript 1 (Malat1). Malat1 RNA is expressed in numerous tissues and is highly abundant in neurons. It is enriched in nuclear speckles only when RNA polymerase II‐dependent transcription is active. Knock‐down studies revealed that Malat1 modulates the recruitment of SR family pre‐mRNA‐splicing factors to the transcription site of a transgene array. DNA microarray analysis in Malat1‐depleted neuroblastoma cells indicates that Malat1 controls the expression of genes involved not only in nuclear processes, but also in synapse function. In cultured hippocampal neurons, knock‐down of Malat1 decreases synaptic density, whereas its over‐expression results in a cell‐autonomous increase in synaptic density. Our results suggest that Malat1 regulates synapse formation by modulating the expression of genes involved in synapse formation and/or maintenance. Malat1 is a long non‐coding RNA that localizes to nuclear speckles, but whose function remains unclear. Here, the Spector and Bessis laboratories show that Malat1 is important for the recruitment of splicing factors to transcription sites, the expression of synaptic genes and as a consequence synaptogenesis.

Key Points The structure of the postsynaptic membrane is highly heterogeneous and dynamic. Receptors are stabilized by a network that consists of scaffold proteins, adhesion proteins and the cytoskeleton, and changes in the receptor profile of the membrane are mediated by endocytosis, exocytosis and diffusion. Receptor diffusion has a role during the formation of new synapses, and during synaptic turnover and synaptic plasticity. There are five main categories of diffusion, ranging from 'free' to 'confined'. The subsynaptic scaffold network constitutes a barrier to receptor movement, resulting in confined diffusion. Techniques such as single particle tracking and fluorescence recovery after photobleaching have been used to follow receptor movements. Fast random movements are interspersed with periods of relative immobility, indicating the presence of transient submicrometre domains in the membrane that are separated by barriers. Within these domains, receptor diffusion is as fast as expected from theoretical calculations. Receptors can escape these 'corrals' by 'jumping the fence' or by passing through gaps when the membrane skeleton is transiently dissociated. Receptors can diffuse individually or as part of a cluster. Clusters are aggregations of receptors that are stabilized by their associations with scaffold components. Diffusion of cluster-associated receptors may be due to movement of the entire cluster or movement of the individual receptor within the cluster. Equilibrium between receptors entering and exiting subdomains (corrals) accounts for the apparent stability of the postsynaptic membrane. So, gross changes in receptor number during synaptogenesis and synaptic plasticity can be considered to result from a change in the set-point of this equilibrium. Neurotransmitter receptor movement into and out of synapses is one of the core mechanisms for rapidly changing the number of functional receptors during synaptic plasticity. Recent data have shown that rapid gain and loss of receptors from synaptic sites are accounted for by endocytosis and exocytosis, as well as by lateral diffusion of receptors in the plane of the membrane. These events are interdependent and are regulated by neuronal activity and interactions with scaffolding proteins. Here we focus on the physical laws that govern receptor diffusion and stabilization, and how this might reshape how we think about the specific regulation of receptor accumulation at synapses.

The dynamic modulation of receptor diffusion-trapping at inhibitory synapses is crucial to synaptic transmission, stability, and plasticity. In this review article, we will outline the progression of understanding of receptor diffusion dynamics at the plasma membrane. We will discuss how regulation of reversible trapping of receptor-scaffold interactions in combination with theoretical modeling approaches can be used to quantify these chemical interactions at the postsynapse of living cells.

Long-term synaptic plasticity is believed to be the cellular substrate of learning and memory. Synaptic plasticity rules are defined by the specific complement of receptors at the synapse and the associated downstream signaling mechanisms. In young rodents, at the cerebellar synapse between granule cells (GC) and Purkinje cells (PC), bidirectional plasticity is shaped by the balance between transcellular nitric oxide (NO) driven by presynaptic N-methyl-D-aspartate receptor (NMDAR) activation and postsynaptic calcium dynamics. However, the role and the location of NMDAR activation in these pathways is still debated in mature animals. Here, we show in adult rodents that NMDARs are present and functional in presynaptic terminals where their activation triggers NO signaling. In addition, we find that selective genetic deletion of presynaptic, but not postsynaptic, NMDARs prevents synaptic plasticity at parallel fiber-PC (PF-PC) synapses. Consistent with this finding, the selective deletion of GC NMDARs affects adaptation of the vestibulo-ocular reflex. Thus, NMDARs presynaptic to PCs are required for bidirectional synaptic plasticity and cerebellar motor learning.

Dieterich et al . describe a methodology to label all newly synthesized neuronal proteins in situ . This method, which they name FUNCAT, relies on the inclusion of noncanonical amino acids and selective fluorescent labeling via click chemistry. The authors show that this system is amenable to dual pulse-chase experiments and dynamic tracking of newly synthesized proteins. Protein translation has been implicated in different forms of synaptic plasticity, but direct in situ visualization of new proteins is limited to one or two proteins at a time. Here we describe a metabolic labeling approach based on incorporation of noncanonical amino acids into proteins followed by chemoselective fluorescence tagging by means of 'click chemistry'. After a brief incubation with azidohomoalanine or homopropargylglycine, a robust fluorescent signal was detected in somata and dendrites. Pulse-chase application of azidohomoalanine and homopropargylglycine allowed visualization of proteins synthesized in two sequential time periods. This technique can be used to detect changes in protein synthesis and to evaluate the fate of proteins synthesized in different cellular compartments. Moreover, using strain-promoted cycloaddition, we explored the dynamics of newly synthesized membrane proteins using single-particle tracking and quantum dots. The newly synthesized proteins showed a broad range of diffusive behaviors, as would be expected for a pool of labeled proteins that is heterogeneous.

The synaptic weight between a pre- and a postsynaptic neuron depends in part on the number of postsynaptic receptors. On the surface of neurons, receptors traffic by random motion in and out from a microstructure called the postsynaptic density (PSD). In the PSD, receptors can be stabilized at the membrane when they bind to scaffolding proteins. We propose a mathematical model to compute the postsynaptic counterpart of the synaptic weight based on receptor trafficking. We take into account the receptor fluxes at the PSD, which can be regulated by neuronal activity, and the interactions of receptors with the scaffolding molecules. Using a Markovian approach, we estimate the mean and the fluctuations of the number of bound receptors. When the number of receptors is large, a deterministic system is also derived. Moreover, these equations can be used, for example, to fit fluorescence-recovery-after-photobleaching experiments to determine, in living neurons, the chemical binding constants for the receptors/scaffolding molecules interaction at synapses.