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Dm9 neurons in Drosophila have been proposed as functional homologs of horizontal cells in the outer retina of vertebrates. Here we combine genetic dissection of neuronal circuit function, two-photon calciumimaging in Dm9 and inner photoreceptors, and immunohistochemical analysis to reveal novel insights into the functional role of Dm9 in early visual processing. Our experiments show that Dm9 receive input from all four types of inner photoreceptor R7p, R7y, R8p, and R8y. Histamine released from all types R7/R8 directly inhibits Dm9 via the histamine receptorOrt, and outweighs simultaneous histamine-independent excitation of Dm9 by UV-sensitive R7. Dm9 in turn provides inhibitory feedback to all R7/R8, which is sufficient for color-opponent processing in R7 but not R8. Color opponent processing in R8 requires additional synaptic inhibition by R7 of the same ommatidium via axo-axonal synapses and the second Drosophila histamine receptor HisCl1. Notably, optogenetic inhibition of Dm9 prohibits color opponent processing in all types of R7/R8 and decreases intracellular calciumin photoreceptor terminals. The latter likely results fromreduced release of excitatory glutamate from Dm9 and shifts overall photoreceptor sensitivity toward higher light intensities. In summary, our results underscore a key role of Dm9 in color opponent processing in Drosophila and suggest a second role of Dm9 in regulating light adaptation in inner photoreceptors. These novel findings on Dm9 are indeed reminiscent of the versatile functions of horizontal cells in the vertebrate retina. [ABSTRACT FROM AUTHOR]

In presynaptic terminals, membrane-delimited Gi/o-mediated presynaptic inhibition is ubiquitous and acts via Gβc to inhibit Ca2+ entry, or directly at SNARE complexes to inhibit Ca21-dependent synaptotagmin-SNARE complex interactions. At CA1-subicular presynaptic terminals, 5-HT1B and GABAB receptors colocalize. GABAB receptors inhibit Ca21 entry, whereas 5-HT1B receptors target SNARE complexes. We demonstrate in male and female rats that GABAB receptors alter Pr, whereas 5-HT1B receptors reduce evoked cleft glutamate concentrations, allowing differential inhibition of AMPAR and NMDAR EPSCs. This reduction in cleft glutamate concentration was confirmed by imaging glutamate release using a genetic sensor (iGluSnFR). Simulations of glutamate release and postsynaptic glutamate receptor currents were made. We tested effects of changes in vesicle numbers undergoing fusion at single synapses, relative placement of fusing vesicles and postsynaptic receptors, and the rate of release of glutamate from a fusion pore. Experimental effects of Pr changes, consistent with GABAB receptor effects, were straightforwardly represented by changes in numbers of synapses. The effects of 5-HT1B receptor-mediated inhibition are well fit by simulated modulation of the release rate of glutamate into the cleft. Colocalization of different actions of GPCRs provides synaptic integration within presynaptic terminals. Train-dependent presynaptic Ca2+ accumulation forces frequency-dependent recovery of neurotransmission during 5-HT1B receptor activation. This is consistent with competition between Ca2+-synaptotagmin and Gβc at SNARE complexes. Thus, stimulus trains in 5-HT1B receptor agonist unveil dynamic synaptic modulation and a sophisticated hippocampal output filter that itself is modulated by colocalized GABAB receptors, which alter presynaptic Ca2+. In combination, these pathways allow complex presynaptic integration. [ABSTRACT FROM AUTHOR]

The canonical hippocampal NMDA memory receptor also controls the release of the transmitter glutamate and the growth factor BDNF.

Neurotransmitter release is a highly controlled process by which synapses can critically regulate information transfer within neural circuits. While presynaptic receptors – typically activated by neurotransmitters and modulated by neuromodulators – provide a powerful way of fine-tuning synaptic function, their contribution to activity-dependent changes in transmitter release remains poorly understood. Here, we report that presynaptic NMDA receptors (preNMDARs) at mossy fiber boutons in the rodent hippocampus can be activated by physiologically relevant patterns of activity and selectively enhance short-term synaptic plasticity at mossy fiber inputs onto CA3 pyramidal cells and mossy cells, but not onto inhibitory interneurons. Moreover, preNMDARs facilitate brain-derived neurotrophic factor release and contribute to presynaptic calcium rise. Taken together, our results indicate that by increasing presynaptic calcium, preNMDARs fine-tune mossy fiber neurotransmission and can control information transfer during dentate granule cell burst activity that normally occur in vivo.

An important pool of chelatable zinc is present in the synaptic vesicles of mossy fiber terminals from hippocampal CA3 area, being zinc released following single or repetitive electrical stimulation. Previous studies have suggested different synaptic roles for released mossy fiber zinc, including the inhibition of presynaptic calcium and of postsynaptic N-methyl-D-aspartate (NMDA) and gamma amino-butiric acid (GABA A) receptors. The effect of endogenously released zinc on mossy fiber long-term potentiation (LTP) induction also is not yet established. We have investigated the effect of the permeant zinc chelator N,N,N',N'-tetrakis(2-pyridylmethyl) ethylenediamine (TPEN) on mossy fiber calcium and on synaptic transmission, before and during the application of LTP-inducing stimulation. We have found, using the calcium indicator Fura-2, that single and tetanically-evoked mossy fiber calcium signals are both enhanced in the presence of 20 μM TPEN, while the single field potentials are unaffected. As expected, no effect was observed on the single calcium signals or field potentials obtained at the CA3-CA1 synapses, from the CA1 area, which has a lower concentration of vesicular zinc. These results support the idea that at the hippocampal mossy fiber synapses, released zinc inhibits presynaptic calcium mechanisms. A higher concentration of TPEN (100 μM) significantly reduced mossy fiber synaptic transmission but did not prevent the induction of mossy fiber LTP, suggesting that zinc is not required for the formation of this form of LTP.

Tight coupling between Ca2+ channels and the sensor for vesicular transmitter release at the presynaptic active zone (AZ) is crucial for high-fidelity synaptic transmission. It has been hypothesized that a switch from a loosely coupled to a tightly coupled transmission mode is a common step in the maturation of CNS synapses. However, this hypothesis has never been tested at cortical synapses. We addressed this hypothesis at a representative small cortical synapse: the synapse connecting mouse cerebellar cortical parallel fibers to Purkinje neurons. We found that the slow Ca2+ chelator EGTA affected release significantly stronger at immature than at mature synapses, while the fast chelator BAPTA was similarly effective in both groups. Analysis of paired-pulse ratios and quantification of release probability (pr) with multiple-probability fluctuation analysis revealed increased facilitation at immature synapses accompanied by reduced pr Cav2.1 Ca2+ channel immunoreactivity, assessed by quantitative high-resolution immuno-electron microscopy, was scattered over immature boutons but confined to putative AZs at mature boutons. Presynaptic Ca2+ signals were quantified with two-photon microscopy and found to be similar between maturation stages. Models adjusted to fit EGTA dose-response curves as well as differential effects of the Ca2+ channel blocker Cd2+ indicate looser and less homogenous coupling at immature terminals compared with mature ones. These results demonstrate functionally relevant developmental tightening of influx-release coupling at a single AZ cortical synapse and corroborate developmental tightening of coupling as a prevalent phenomenon in the mammalian brain. [ABSTRACT FROM AUTHOR]

Synaptic short-term plasticity is a key regulator of neuronal communication and is controlled via various mechanisms. A well established property of mossy fiber to CA3 pyramidal cell synapses is the extensive short-term facilitation during high-frequency bursts. We investigated the mechanisms governing facilitation using a combination of whole-cell electrophysiological recordings, electrical minimal stimulation, and random-access two-photon microscopy in acute mouse hippocampal slices. Two distinct presynaptic mechanisms were involved in short-term facilitation, with their relative contribution dependent on extracellular calcium concentration. The synchronization of multivesicular release was observed during trains of facilitating EPSCs recorded in 1.2 mM external Ca2+ ([Ca2+]e). Indeed, covariance analysis revealed a gradual augmentation in quantal size during trains of EPSCs, and application of the low-affinity glutamate receptor antagonist y-D-glutamylglycine showed an increase in cleft glutamate concentration during paired-pulse stimulation. Whereas synchronization of multivesicular release contributed to the facilitation in 1.2 mM [Ca2+]e, variance-mean analysis showed that recruitment of more release sites (JV) was likely to account for the larger facilitation observed in 2.5 mM [Ca2+]e. Furthermore, this increase in N could be promoted by calcium microdomains of heterogeneous amplitudes observed in single mossy fiber boutons. Our findings suggest that the combination of multivesicular release and the recruitment of additional release sites act together to increase glutamate release during burst activity. This is supported by the compartmentalized spatial profile of calcium elevations in boutons and helps to expand the dynamic range of mossy fibers information transfer. [ABSTRACT FROM AUTHOR]

Morphological studies have provided ample evidence for synaptic connections between cerebellar Purkinje cells (PCs), but the functional properties of these synapses remain elusive. We report on direct recordings of synaptically connected PC5 in mice cerebellar slices. In PCs filled with a fluorescent dye to aid axon visualization and postsynaptic target identification, presynaptic action potentials elicited unitary inhibitory postsynaptic currents in neighboring PCs in 10% of potential connections tested. In 11 pairs. postsynaptic currents had a delay onset of 1.62 ± 0.16 ms with respect to the presynaptic spike, a 10—90% rise time of 2.20 ± 0.33 ms. and a monoexponential decay with a time constant of 13.3 ± 1.7 ms. Average values for peak current and variance-to-mean ratio were 55 ± 14 and 30 ± 3 pA, respectively. In contrast to the depressing nature of the synapse between PC5 and deep cerebellar nuclei neurons, PC-PC synapses exhibited strong facilitation operating within a time window of a few milliseconds; paired-pulse ratios for 3-and 20-ms intervals were 1.79 ± 0.18 and 1.01 ± 0.14, respectively (n = 6). The facilitation is of presynaptic nature because it is accompanied by a decrease in failure rate. Trains of action potentials evoked in presynaptic varicosities volume-averaged calcium transients whose peak increased 1.7-fold as the frequency increased from 50 to 166 Hz. We suggest that PC-PC synapses are tuned for high fidelity of transmission during bursts of PC activity and that their operation in the cerebellar circuit modulates synchronized PC firing. [ABSTRACT FROM AUTHOR]

Activity-dependent elevation of calcium within presynaptic boutons regulates many aspects of synaptic transmission. Here, we examine presynaptic residual calcium (Cares) transients in individual presynaptic boutons of cerebellar granule cells at near-physiological temperatures using two-photon microscopy. Properties of Cares under conditions of zero-added buffer were determined by measuring Cares transients while loading boutons to a steady-state indicator concentration. These experiments revealed that, in the absence of exogenous calcium buffers, a single action potential evokes transients of Cares that vary widely in different boutons both in amplitude (400-900 nM) and time course (25-55 ms). Variation in calcium influx density, endogenous buffer capacity, and calcium extrusion density contribute to differences in Cares among boutons. Heterogeneity in Cares within different boutons suggests that plasticity can be regulated independently at different synapses arising from an individual granule cell. In a given bouton, Cares signals were highly reproducible from trial to trial and failures of calcium influx were not observed. We find that a factor contributing to this reliability is that an action potential opens a large number of calcium channels (20-125) in a bouton. Presynaptic calcium signals were also used to assess the ability of granule cell axons to convey somatically generated action potentials to distant synapses. In response to pairs of action potentials or trains, granule cell boutons showed a remarkable ability to respond reliably at frequencies up to 500 Hz. Thus, individual boutons appear specialized for reliable calcium signaling during bursts of high-frequency activation such as those that are observed in vivo. [ABSTRACT FROM AUTHOR]

The hippocampal mossy fiber long-term potentiation (LTP) is an N-methyl-d-aspartate (NMDA) receptor-independent form of long-lasting synaptic plasticity characteristic of the zinc-enriched mossy fiber synapses. Its expression is generally considered to have a presynaptic locus and to be mediated by a persistent increase of evoked transmitter release. Because the release process is calcium-dependent, the observed increase in synaptic efficacy could be due to a persistent modification of presynaptic calcium mechanisms, triggered by the large calcium influx associated with long-term potentiation induction. Alternatively, it might be caused by an enhancement in the sensitivity to calcium of some components of the synaptic vesicle release system, following the large intraterminal calcium accumulation. We investigated the first hypothesis by measuring presynaptic Fura-2 calcium signals associated with electrically induced mossy fiber long-term potentiation. We have observed that like residual calcium, single presynaptic calcium changes are not enhanced during the maintenance phase of mossy fiber long-term potentiation. This result supports the idea that this form of long-term potentiation may be mediated by persistent changes of some process occurring after calcium entry. It has been established that voltage-dependent calcium channels are inhibited by zinc and that endogenous zinc is released in a calcium-dependent way following intense mossy fiber activation. Because there is evidence that at these synapses zinc is also released following single electrical stimulation, we investigated the effect of endogenous zinc on single presynaptic calcium signals and on field potentials associated with mossy fiber LTP. We have observed that this form of LTP could be induced in the presence of the permeant heavy metal chelator N,N,N′,N′-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN) and that application of this chelator, during LTP, caused an enhancement of the presynaptic calcium signals without affecting synaptic transmission. This enhancement is consistent with the idea that mossy fiber zinc, released following individual stimuli, inhibits presynaptic calcium mechanisms. [Copyright &y& Elsevier]

Although the endoplasmic reticulum (ER) is present throughout axons, and IP 3 and ryanodine receptors are widely expressed in nerve terminals, whether Ca2+ release from presynaptic stores contributes to action potential (AP)-evoked Ca2+ transients remains controversial. We investigated the release of Ca2+ from ER stores in boutons en passant of neocortical layer 5 pyramidal neurons. A hallmark of these stores is that they spontaneously release Ca2+ at a low frequency. Using a high-affinity Ca2+ indicator, we documented and characterised such spontaneous Ca2+ transients (sCaTs), which occurred at a rate of ~0.2 per min and raised the intracellular Ca2+ concentration ([Ca2+] i) by ~2 µM in the absence of exogenous buffers. Caffeine increased the average frequency of sCaTs by 90%, without affecting their amplitude and decay kinetics. Therefore, presynaptic ryanodine receptors were likely involved. To determine if presynaptic ER stores contribute to intracellular Ca2+ accumulation during repetitive stimulation, we measured [Ca2+] i during 2 s long trains of APs evoked at 10–50 Hz. We found that for frequencies <20 Hz, [Ca2+] i reached a steady state within ~500 ms after stimulation onset. However, for higher frequencies, [Ca2+] i continued to increase with AP number, suggesting that the rate of Ca2+ entry exceeded the rate of clearance. Comparison between measured and predicted values indicates supralinear summation of Ca2+. Block of the sarco/endoplasmic reticulum Ca2+-ATPase reduced the supralinearity of summation, without reducing the amplitude of a single AP-evoked Ca2+ transient. Together, our results implicate presynaptic ER stores as a source of Ca2+ during repetitive stimulation. • Spontaneous Ca2+ transients are observed in boutons en passant. • The frequency of these transients is increased by caffeine. • During repetitive high-frequency firing, presynaptic Ca2+ sums supralinearly. • Block of SERCA pump reduces the supralinearity of summation. • Store release underlies the supralinear increase of presynaptic Ca2+. [Display omitted] [ABSTRACT FROM AUTHOR]

The canonical hippocampal NMDA memory receptor also controls the release of the transmitter glutamate and the growth factor BDNF., Competing Interests: HW, OC, PS No competing interests declared, (© 2021, Wong et al.)

Presynaptic Ca V 2 channels are essential for Ca2+-triggered exocytosis. In addition, there are two competing models for their roles in synapse structure. First, Ca2+ channels or Ca2+ entry may control synapse assembly. Second, active zone proteins may scaffold Ca V 2s to presynaptic release sites, and synapse structure is Ca V 2 independent. Here, we ablated all three Ca V 2s using conditional knockout in cultured hippocampal neurons or at the calyx of Held, which abolished evoked exocytosis. Compellingly, synapse and active zone structure, vesicle docking, and transsynaptic nano-organization were unimpaired. Similarly, long-term blockade of action potentials and Ca2+ entry did not disrupt active zone assembly. Although Ca V 2 knockout impaired the localization of β subunits, α2δ-1 localized normally. Rescue with Ca V 2 restored exocytosis, and Ca V 2 active zone targeting depended on the intracellular C-terminus. We conclude that synapse assembly is independent of Ca V 2s or Ca2+ entry through them. Instead, active zone proteins recruit and anchor Ca V 2s via Ca V 2 C-termini. • Ca V 2s mediate evoked synaptic vesicle release and cannot be replaced by Ca V 1 or Ca V 3 • Active zone nano-assemblies and docking persist after removing Ca V 2s or Ca2+ entry • α2δ-1 localization within nerve terminals is broad and does not require Ca V 2s • Ca V 2 C-termini and their binding to active zone proteins mediate Ca V 2 targeting Ca V 2 channels provide Ca2+ for triggering neurotransmitter release at central synapses. Held et al. remove all Ca V 2s and Ca2+ entry and find that synaptic protein nano-assemblies persist and synapse ultrastructure is unimpaired despite abolishing synaptic transmission. Rescue experiments establish that Ca V 2 C-termini are important for channel anchoring at active zones. [ABSTRACT FROM AUTHOR]

Although the endoplasmic reticulum (ER) is present throughout axons, and IP 3 and ryanodine receptors are widely expressed in nerve terminals, whether Ca 2+ release from presynaptic stores contributes to action potential (AP)-evoked Ca 2+ transients remains controversial. We investigated the release of Ca 2+ from ER stores in boutons en passant of neocortical layer 5 pyramidal neurons. A hallmark of these stores is that they spontaneously release Ca 2+ at a low frequency. Using a high-affinity Ca 2+ indicator, we documented and characterised such spontaneous Ca 2+ transients (sCaTs), which occurred at a rate of ~0.2 per min and raised the intracellular Ca 2+ concentration ([Ca 2+ ] i ) by ~2 µM in the absence of exogenous buffers. Caffeine increased the average frequency of sCaTs by 90%, without affecting their amplitude and decay kinetics. Therefore, presynaptic ryanodine receptors were likely involved. To determine if presynaptic ER stores contribute to intracellular Ca 2+ accumulation during repetitive stimulation, we measured [Ca 2+ ] i during 2 s long trains of APs evoked at 10-50 Hz. We found that for frequencies <20 Hz, [Ca 2+ ] i reached a steady state within ~500 ms after stimulation onset. However, for higher frequencies, [Ca 2+ ] i continued to increase with AP number, suggesting that the rate of Ca 2+ entry exceeded the rate of clearance. Comparison between measured and predicted values indicates supralinear summation of Ca 2+ . Block of the sarco/endoplasmic reticulum Ca 2+ -ATPase reduced the supralinearity of summation, without reducing the amplitude of a single AP-evoked Ca 2+ transient. Together, our results implicate presynaptic ER stores as a source of Ca 2+ during repetitive stimulation., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Neurotransmitter release is a highly controlled process by which synapses can critically regulate information transfer within neural circuits. While presynaptic receptors - typically activated by neurotransmitters and modulated by neuromodulators - provide a powerful way of fine-tuning synaptic function, their contribution to activity-dependent changes in transmitter release remains poorly understood. Here, we report that presynaptic NMDA receptors (preNMDARs) at mossy fiber boutons in the rodent hippocampus can be activated by physiologically relevant patterns of activity and selectively enhance short-term synaptic plasticity at mossy fiber inputs onto CA3 pyramidal cells and mossy cells, but not onto inhibitory interneurons. Moreover, preNMDARs facilitate brain-derived neurotrophic factor release and contribute to presynaptic calcium rise. Taken together, our results indicate that by increasing presynaptic calcium, preNMDARs fine-tune mossy fiber neurotransmission and can control information transfer during dentate granule cell burst activity that normally occur in vivo., Competing Interests: PL, HK, KA, RL, PC No competing interests declared, (© 2021, Lituma et al.)

The loss of cognitive function accompanying healthy aging is not associated with extensive or characteristic patterns of cell death, suggesting it is caused by more subtle changes in synaptic properties. In the hippocampal CA1 region, long‐term potentiation requires stronger stimulation for induction in aged rats and mice and long‐term depression becomes more prevalent. An age‐dependent impairment of postsynaptic calcium homeostasis may underpin these effects. We have examined changes in presynaptic calcium signalling in aged mice using a transgenic mouse line (SyG37) that expresses a genetically encoded calcium sensor in presynaptic terminals. SyG37 mice showed an age‐dependent decline in cognitive abilities in behavioural tasks that require hippocampal processing including the Barnes maze, T‐maze and object location but not recognition tests. The incidence of LTP was significantly impaired in animals over 18 months of age. These effects of aging were accompanied by a persistent increase in resting presynaptic calcium, an increase in the presynaptic calcium signal following Schaffer collateral fibre stimulation, an increase in postsynaptic fEPSP slope and a reduction in paired‐pulse facilitation. These effects were not caused by synapse proliferation and were of presynaptic origin since they were evident in single presynaptic boutons. Aged synapses behaved like younger ones when the extracellular calcium concentration was reduced. Raising extracellular calcium had little effect on aged synapses but altered the properties of young synapses into those of their aged counterparts. These effects can be readily explained by an age‐dependent change in the properties or numbers of presynaptic calcium channels. [ABSTRACT FROM AUTHOR]

Summary Color vision extracts spectral information by comparing signals from photoreceptors with different visual pigments. Such comparisons are encoded by color-opponent neurons that are excited at one wavelength and inhibited at another. Here, we examine the circuit implementation of color-opponent processing in the Drosophila visual system by combining two-photon calcium imaging with genetic dissection of visual circuits. We report that color-opponent processing of UV short /blue and UV long /green is already implemented in R7/R8 inner photoreceptor terminals of “pale” and “yellow” ommatidia, respectively. R7 and R8 photoreceptors of the same type of ommatidia mutually inhibit each other directly via HisCl1 histamine receptors and receive additional feedback inhibition that requires the second histamine receptor Ort. Color-opponent processing at the first visual synapse represents an unexpected commonality between Drosophila and vertebrates; however, the differences in the molecular and cellular implementation suggest that the same principles evolved independently. [ABSTRACT FROM AUTHOR]