Abstract
The presynaptic active zone (AZ) of chemical synapses is a highly dynamic compartment where synaptic vesicle fusion and neurotransmitter release take place. During evolution the AZ was optimized for speed, accuracy, and reliability of chemical synaptic transmission in combination with miniaturization and plasticity. Single-molecule localization microscopy (SMLM) offers nanometer spatial resolution as well as information about copy number, localization, and orientation of proteins of interest in AZs. This type of imaging allows quantifications of activity dependent AZ reorganizations, e.g., in the context of presynaptic homeostatic potentiation. In combination with high-pressure freezing and optogenetic or electrical stimulation AZs can be imaged with millisecond temporal resolution during synaptic activity. Therefore SMLM allows the determination of key parameters in the complex spatial environment of AZs, necessary for next generation simulations of chemical synapses with realistic protein arrangements.
Introduction
Presynaptic Active Zones and Synaptic Vesicles
Neurotransmitter release at presynaptic active zones (AZs) of chemical synapses is currently investigated intensely and was recently reviewed from various perspectives (Brunger et al., 2018; Silva et al., 2021; Werner et al., 2021; Rizo, 2022; Wichmann and Kuner, 2022). Since the term AZ was coined in the last century (Tsuji, 2006) substantial progress occurred. As in any research field, quite obviously, specific techniques such as electron microscopy (EM), molecular genetics, structural biology, and patch clamp electrophysiology provide complementary data. In view of decades of research, it remains fascinating to witness how preparations and techniques for AZ research are continuously refined and more precise quantitative information accumulates.
Electron microscopy of AZs continues to provide critical insights, as for example was recently shown for structural transitions during synaptic vesicle (SV) priming (Grushin et al., 2022; Lichter et al., 2022). Evaluating the dimensions of electron dense material below docked SVs can provide information how the chaperone Munc13, synaptotagmin, SNARE complexes, and complexins are assembled (Rothman et al., 2017; Zhou et al., 2017). Furthermore, the combination of EM and high pressure freezing (HPF) with optical stimulation, aptly termed flash-and-freeze (Watanabe et al., 2013a,b; Chang et al., 2018; Borges-Merjane et al., 2020; Imig et al., 2020; Vandael et al., 2020), or electrical stimulation (zap-and-freeze, Kusick et al., 2020; Li et al., 2021; Vevea et al., 2021), brings certainly more than just a breath of fresh air to the field. Flash-and-freeze or zap-and-freeze provide millisecond resolution for activity dependent imaging of SVs in AZs. Although it is difficult to make predictions, especially about the future, it is probably safe to expect further substantial progress along this line of investigation.
We focus on yet another technique for super-resolution of SVs and AZs, namely localization microscopy in the form of direct stochastic optical reconstruction microscopy (dSTORM; van de Linde et al., 2011). dSTORM offers protein specificity and in ideal cases spatial resolutions of several nanometers. This was nicely demonstrated for nuclear pore complexes (Löschberger et al., 2012, 2014), which despite inherent flexibility (Schuller et al., 2021), are used as reference standards for quantitative super-resolution microscopy (Thevathasan et al., 2019). In the following we will: (1) present paradigmatic dSTORM data for two types of synapses, (2) discuss dSTORM of activity dependent AZ rearrangements, (3) return to the above-mentioned combination of HPF with either optical or electrical stimulation and will argue how dSTORM of AZs may profit from HPF with stimulation, and (4) end by touching the topic how a realistic ultrastructure can be achieved in next generation simulations of SVs in AZs.
Results and Discussion
Distinct Presynaptic Active Zones
Images of the abundant presynaptic AZ scaffolding protein Bassoon (Gundelfinger et al., 2016) in two chemical synapses of a mouse serve to introduce dSTORM images of AZs. The left panel in Figure 1A shows a representative Bassoon cluster in an endplate of a neuromuscular junction (NMJ). The left panel in Figure 1B illustrates a representative Bassoon cluster in a cerebellar parallel fiber (PF). The right panels in Figure 1 show histograms of cluster length in the two preparations. The experimental imaging was essentially performed as described earlier for 2D dSTORM in 1 μm thick tissue sections (Pauli et al., 2021). The substantial difference in Bassoon cluster length in Figures 1A,B is absolutely obvious and fits quite well to EM data of AZ dimensions in the two preparations (Nagwaney et al., 2009; Indriati et al., 2013). Since protein amount can be measured with dSTORM by quantifying the fluorescence signal, more precisely the number of localizations (Löschberger et al., 2012, 2014; Ehmann et al., 2014), the two images in the left panels of Figure 1 also reveal that the Bassoon content of endplate AZs is certainly much lower than that of PF AZs. Significant differences of Bassoon cluster length, localizations per cluster (Bassoon content) and cluster volumes were also measured recently for three types of hippocampal principal neurons, even within single tissue sections, using dSTORM (Figure 4 in Pauli et al., 2021). In principle, protein specific quantitative results with dSTORM for AZs are similar to data obtained by freeze-fracture replica immunogold labeling (Hagiwara et al., 2005; Éltes et al., 2017; Mrestani et al., 2021; Pauli et al., 2021). Figure 1 serves as illustration that it is possible to measure the amount and the distribution of proteins of interest in AZs with dSTORM.
FIGURE 1
Presynaptic Bassoon AZ scaffold in two murine synaptic connections. (A) The left panel shows a representative 2D one-color dSTORM image of a Bassoon cluster in a mouse motor endplate of a Levator auris muscle preparation. On the right a histogram for Bassoon cluster length is displayed (n = 34 AZs, length = 120 ± 35 nm, mean ± SD). (B) The left panel shows a dSTORM image of a Bassoon cluster in a parallel fiber to Purkinje neuron synapse in a sagittal cryosection of a mouse cerebellar vermis. On the right again, a histogram for Bassoon cluster length is shown (n = 184 AZs, length = 520 ± 88 nm).
Activity Dependent Rearrangements
While protein distribution measurements with scale bars of 300 nm (Figure 1) are valuable, another level is reached by more detailed evaluations of the fine structure of dSTORM data. For the Drosophila NMJ, it was reported that the AZ cytomatrix is composed of units containing approximately 137 copies of Bruchpilot (Brp) protein, three quarters of which are organized into about 15 heptameric clusters (Ehmann et al., 2014). Bassoon and Brp are often used as AZ markers, since they are relatively abundant AZ proteins.
More recently, hierarchical density-based spatial clustering of applications with noise (HDBSCAN) was used to study Brp distribution and AZ plasticity during presynaptic homeostatic potentiation (PHP; Mrestani et al., 2021; Figure 2). Compaction of individual AZs was found in acute philanthotoxin-induced and chronic genetically induced PHP but Brp protein copy numbers did not change. Compaction occurs even at the level of Brp subclusters (SCs), which additionally move toward AZ centers. Furthermore, compaction happens also within SCs of Rab3 interacting molecule-binding protein (RBP), another AZ protein closer to the membrane (Mrestani et al., 2021). Brp SCs in wild type have average diameters of about 46 nm, compared to a diameter of about 27 nm for RBP SCs (Mrestani et al., 2021, note scale difference in Figures 2B,C). Furthermore, RBP SCs contain only about 1/3 of the localizations of Brp SCs, and RBP is thus less abundant in AZs (Mrestani et al., 2021). However, other proteins, such as calcium channel subunits, are again substantially less abundant than RBP, but still readily detectable in AZs with dSTORM and related techniques (Ehmann et al., 2015; Newman et al., 2022). AZ proteins can also be arranged in still smaller clusters with diameters well below the diameter of a typical SV, approaching the localization precision of about 6 nm in our dSTORM images (Mrestani et al., 2021). It might thus be possible to obtain activity dependent dSTORM protein maps, e.g., for presynaptic calcium channels or other less abundant AZ proteins.
FIGURE 2
Compaction of presynaptic AZ SCs (A) HDBSCAN for SC detection applied to an AZ of a wild-type Ib bouton of a Drosophila melanogaster neuromuscular junction stained for BrpNC82. Black lines indicate alpha shapes used for AZ area quantification. Left: colored Brp SCs surrounded by colored lines indicating alpha shapes. Gray dots represent unclustered localizations. Right: centers of mass (c.o.m.) of the AZ (cross) and of SCs (colored dots) are indicated. A dashed line shows the Euclidean distance between the AZ c.o.m. and an SC c.o.m., referred to as radial distance. Scale bar 100 nm. (B) Chronic PHP (GluRIIAko) decreases Brp SC area. Scatterplots of Ib AZs from control (ctrl) and GluRIIAko animals. (C) Compaction of RBP SCs at GluRIIAko AZs. Scatterplots of Ib AZs from control (ctrl) and GluRIIAko animals. Reprinted from Mrestani et al. (2021). ***p < 0.001.
High Pressure Freezing, Stimulation, and Direct Stochastic Optical Reconstruction Microscopy of Active Zones
Facing activity dependent positional changes of AZ proteins with dSTORM, we are led to ask: What could be gained by combining dSTORM with flash- or zap-and-freeze? HPF alone eliminates artifacts commonly associated with classical chemical fixation. More fascinating is, that dSTORM after flash- or zap-and-freeze should yield AZ protein maps with millisecond temporal resolution after synaptic stimulations. While it is not entirely clear how much spatiotemporal protein changes we will find with such investigations, it is instructive to speculate briefly about such experiments. Protein arrangements of SVs change during fusion (Brunger et al., 2018; Rizo, 2022). Perhaps more subtle protein repositioning during SV fusion will remain invisible with currently achievable dSTORM. However, larger protein displacements such as, e.g., the ones of complexin and Rab3 during SV fusion might be resolvable. Furthermore, other quantitative predictions, such as the hexameric arrangement of Munc13 below docked SVs, or the position of synaptotagmin on SVs (Rothman et al., 2017; Grushin et al., 2022) could be experimentally tested. We should probably move from whole mounts or currently used 1 μm thick tissue to thinner sections, for these experiments. A section thicknesses of 50 nm or below, and thus in the range of the diameter of individual SVs or even below, might be ideal. Perhaps even serial sections or correlative light and electron microscopy (CLEM) should be tested (Markert et al., 2016). Furthermore, beyond inspections of individual SVs it may be instructive to map the AZ scaffold further with millisecond resolution during the SV cycle with single-molecule localization microscopy (SMLM).
Next Generation Simulations
Models of SVs and AZs should be built considering all available data and thus be reality based. With increasingly detailed ultrastructural data for SV and AZ proteins the mesoscale, bridging the atomic nanoscale and the cellular microscale, still remains largely invisible (Goodsell et al., 2020). This shortcoming can be addressed and we argued above how critical information regarding copy number, localization, and orientation of key SV and AZ proteins can be obtained with dSTORM. It appears the time is ripe for further measurements of activity dependent protein rearrangements of SVs and AZs with SMLM. This might in turn set the stage for next generation simulations of chemical synapses with a more realistic protein nano-architecture.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Statements
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
Ethical review and approval was not required for the animal study because according to German regulation tissue was taken from sacrificed animals.
Author contributions
MH and MP conceived, wrote, and revised the manuscript. Both authors approved the submitted version.
Funding
This work was supported by the German Research Foundation (DFG) project B06 of CRC166; P1 of FOR3004 SYNABS and by the Interdisciplinary Clinical Research Center (IZKF) Würzburg project N-229 to MH.
Acknowledgments
We thank F. Köhler and M. Oppmann for excellent technical assistance and K. Lippmann for comments on the manuscript.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
1
Borges-MerjaneC.KimO.JonasP. (2020). Functional electron microscopy, “flash and freeze,” of identified cortical synapses in acute brain slices.Neuron105992.e–1006.e. 10.1016/j.neuron.2019.12.022
2
BrungerA. T.ChoiU. B.LaiY.LeitzJ.ZhouQ. (2018). molecular mechanisms of fast neurotransmitter release.Annu. Rev. Biophys.47469–497. 10.1146/annurev-biophys-070816-034117
3
ChangS.TrimbuchT.RosenmundC. (2018). Synaptotagmin-1 drives synchronous Ca2+-triggered fusion by C2B-domain-mediated synaptic-vesicle-membrane attachment.Nat. Neurosci.2133–40. Epub 2017 Dec 11. 10.1038/s41593-017-0037-5
4
EhmannN.SauerM.KittelR. J. (2015). Super-resolution microscopy of the synaptic active zone.Front. Cell. Neurosci.9:7. 10.3389/fncel.2015.00007
5
EhmannN.van de LindeS.AlonA.LjaschenkoD.KeungX. Z.HolmT.et al (2014). Quantitative super-resolution imaging of bruchpilot distinguishes active zone states.Nat. Commun.5:4650. 10.1038/ncomms5650
6
ÉltesT.KirizsT.NusserZ.HolderithN. (2017). Target cell type-dependent differences in Ca2+ channel function underlie distinct release probabilities at hippocampal glutamatergic terminals.J. Neurosci.371910–1924. 10.1523/JNEUROSCI.2024-16.2017
7
GoodsellD. S.OlsonA. J.ForliS. (2020). Art and science of the cellular mesoscale.Trends Biochem. Sci.45472–483. 10.1016/j.tibs.2020.02.010
8
GrushinK.Kalyana SundaramR. V.SindelarC. V.RothmanJ. E. (2022). Munc13 structural transitions and oligomers that may choreograph successive stages in vesicle priming for neurotransmitter release.Proc. Natl. Acad. Sci. U.S.A.119:e2121259119. 10.1073/pnas.2121259119
9
GundelfingerE. D.ReissnerC.GarnerC. C. (2016). Role of bassoon and piccolo in assembly and molecular organization of the active zone.Front. Synaptic Neurosci.7:19. 10.3389/fnsyn.2015.00019
10
HagiwaraA.FukazawaY.Deguchi-TawaradaM.OhtsukaT.ShigemotoR. (2005). Differential distribution of release-related proteins in the hippocampal CA3 area as revealed by freeze-fracture replica labeling.J. Comp. Neurol.489195–216. 10.1002/cne.20633
11
ImigC.López-MurciaF. J.MausL.García-PlazaI. H.MortensenL. S.SchwarkM.et al (2020). Ultrastructural imaging of activity-dependent synaptic membrane-trafficking events in cultured brain slices.Neuron108843.e–860.e. 10.1016/j.neuron.2020.09.004
12
IndriatiD. W.KamasawaN.MatsuiK.MeredithA. L.WatanabeM.ShigemotoR. (2013). Quantitative localization of Cav2.1 (P/Q-type) voltage-dependent calcium channels in Purkinje cells: somatodendritic gradient and distinct somatic coclustering with calcium-activated potassium channels.J. Neurosci.333668–3678. 10.1523/JNEUROSCI.2921-12.2013
13
KusickG. F.ChinM.RaychaudhuriS.LippmannK.AdulaK. P.HujberE. J.et al (2020). Synaptic vesicles transiently dock to refill release sites.Nat. Neurosci.231329–1338. 10.1038/s41593-020-00716-1
14
LiS.RaychaudhuriS.LeeS. A.BrockmannM. M.WangJ.KusickG.et al (2021). Asynchronous release sites align with NMDA receptors in mouse hippocampal synapses.Nat. Commun.12:677. 10.1038/s41467-021-21004-x
15
LichterK.PaulM. M.PauliM.SchochS.KollmannsbergerP.StigloherC.et al (2022). Ultrastructural analysis of wildtype and RIM1α knock-out active zones in a large cortical synapse.[Preprint] biorxiv 2022.03.04.482996
16
LöschbergerA.FrankeC.KrohneG.van de LindeS.SauerM. (2014). Correlative super-resolution fluorescence and electron microscopy of the nuclear pore complex with molecular resolution.J. Cell. Sci.1274351–4355. 10.1242/jcs.156620
17
LöschbergerA.van de LindeS.DabauvalleM. C.RiegerB.HeilemannM.KrohneG.et al (2012). Super-resolution imaging visualizes the eightfold symmetry of gp210 proteins around the nuclear pore complex and resolves the central channel with nanometer resolution.J. Cell. Sci.125570–575. 10.1242/jcs.098822
18
MarkertS. M.BritzS.ProppertS.LangM.WitvlietD.MulcahyB.et al (2016). Filling the gap: adding super-resolution to array tomography for correlated ultrastructural and molecular identification of electrical synapses at the C. elegans connectome.Neurophotonics3:041802. 10.1117/1.NPh.3.4.041802
19
MrestaniA.PauliM.KollmannsbergerP.ReppF.KittelR. J.EilersJ.et al (2021). Active zone compaction correlates with presynaptic homeostatic potentiation.Cell Rep.37:109770. 10.1016/j.celrep.2021.109770
20
NagwaneyS.HarlowM. L.JungJ. H.SzuleJ. A.RessD.XuJ.et al (2009). Macromolecular connections of active zone material to docked synaptic vesicles and presynaptic membrane at neuromuscular junctions of mouse.J. Comp. Neurol.513457–468. 10.1002/cne.21975
21
NewmanZ. L.BakshinskayaD.SchultzR.KennyS. J.MoonS.AghiK.et al (2022). Determinants of synapse diversity revealed by super-resolution quantal transmission and active zone imaging.Nat. Commun.13:229. 10.1038/s41467-021-27815-2
22
PauliM.PaulM. M.ProppertS.MrestaniA.SharifiM.ReppF.et al (2021). Targeted volumetric single-molecule localization microscopy of defined presynaptic structures in brain sections.Commun. Biol.4:407. 10.1038/s42003-021-01939-z
23
RizoJ. (2022). Molecular mechanisms underlying neurotransmitter release.Annu. Rev. Biophys.51, 377–408. 10.1146/annurev-biophys-111821-104732
24
RothmanJ. E.KrishnakumarS. S.GrushinK.PincetF. (2017). Hypothesis - buttressed rings assemble, clamp, and release SNAREpins for synaptic transmission.FEBS Lett.5913459–3480. 10.1002/1873-3468.12874
25
SchullerA. P.WojtynekM.MankusD.TatliM.Kronenberg-TengaR.RegmiS. G.et al (2021). The cellular environment shapes the nuclear pore complex architecture.Nature598667–671. 10.1038/s41586-021-03985-3
26
SilvaM.TranV.MartyA. (2021). Calcium-dependent docking of synaptic vesicles.Trends Neurosci.44579–592. 10.1016/j.tins.2021.04.003
27
ThevathasanJ. V.KahnwaldM.CieślińskiK.HoessP.PenetiS. K.ReitbergerM.et al (2019). Nuclear pores as versatile reference standards for quantitative superresolution microscopy.Nat. Methods161045–1053. 10.1038/s41592-019-0574-9
28
TsujiS. (2006). Rene Couteaux (1909-1999) and the morphological identification of synapses.Biol. Cell.98503–509. 10.1042/BC20050036
29
van de LindeS.LöschbergerA.KleinT.HeidbrederM.WolterS.HeilemannM.et al (2011). Direct stochastic optical reconstruction microscopy with standard fluorescent probes.Nat. Protoc.6991–1009. 10.1038/nprot.2011.336
30
VandaelD.Borges-MerjaneC.ZhangX.JonasP. (2020). Short-term plasticity at hippocampal mossy fiber synapses is induced by natural activity patterns and associated with vesicle pool engram formation.Neuron107509.e–521.e. 10.1016/j.neuron.2020.05.013
31
VeveaJ. D.KusickG. F.CourtneyK. C.ChenE.WatanabeS.ChapmanE. R. (2021). Synaptotagmin 7 is targeted to the axonal plasma membrane through γ-secretase processing to promote synaptic vesicle docking in mouse hippocampal neurons.Elife10:e67261. 10.7554/eLife.67261
32
WatanabeS.LiuQ.DavisM. W.HollopeterG.ThomasN.JorgensenN. B.et al (2013a). Ultrafast endocytosis at caenorhabditis elegans neuromuscular junctions.Elife2:e00723. 10.7554/eLife.00723
33
WatanabeS.RostB. R.Camacho-PérezM.DavisM. W.Söhl-KielczynskiB.RosenmundC.et al (2013b). Ultrafast endocytosis at mouse hippocampal synapses.Nature504242–247. Epub 2013 Dec 4. 10.1038/nature12809
34
WernerC.SauerM.GeisC. (2021). Super-resolving microscopy in neuroscience.Chem. Rev.12111971–12015. 10.1021/acs.chemrev.0c01174
35
WichmannC.KunerT. (2022). Heterogeneity of glutamatergic synapses: cellular mechanisms and network consequences.Physiol. Rev.102269–318. 10.1152/physrev.00039.2020
36
ZhouQ.ZhouP.WangA. L.WuD.ZhaoM.SüdhofT. C.et al (2017). The primed SNARE-complexin-synaptotagmin complex for neuronal exocytosis.Nature548420–425. 10.1038/nature23484
Summary
Keywords
active zone, depression, facilitation, plasticity, potentiation, synapse
Citation
Heckmann M and Pauli M (2022) Visualizing Presynaptic Active Zones and Synaptic Vesicles. Front. Synaptic Neurosci. 14:901341. doi: 10.3389/fnsyn.2022.901341
Received
21 March 2022
Accepted
21 April 2022
Published
18 May 2022
Volume
14 - 2022
Edited by
Jae Hoon Jung, National Institutes of Health (NIH), United States
Reviewed by
Silvio O. Rizzoli, Max Planck Society, Germany
Updates
Copyright
© 2022 Heckmann and Pauli.
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*Correspondence: Manfred Heckmann, heckmann@uni-wuerzburg.deMartin Pauli, martin.pauli@uni-wuerzburg.de
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.