PP2A phosphatase is required for dendrite pruning via actin regulation in Drosophila

Abstract Large‐scale pruning, the developmentally regulated degeneration of axons or dendrites, is an important specificity mechanism during neuronal circuit formation. The peripheral sensory class IV dendritic arborization (c4da) neurons of Drosophila larvae specifically prune their dendrites at the onset of metamorphosis in an ecdysone‐dependent manner. Dendrite pruning requires local cytoskeleton remodeling, and the actin‐severing enzyme Mical is an important ecdysone target. In a screen for pruning factors, we identified the protein phosphatase 2 A (PP2A). PP2A interacts genetically with the actin‐severing enzymes Mical and cofilin as well as other actin regulators during pruning. Moreover, Drosophila cofilin undergoes a change in localization at the onset of metamorphosis indicative of a change in actin dynamics. This change is abolished both upon loss of Mical and PP2A. We conclude that PP2A regulates actin dynamics during dendrite pruning.


Introduction
Neurite pruning, the physiological degeneration of axons or dendrites during development, is an important specificity mechanism during neuronal circuit formation [1,2]. While the mechanisms of neurite outgrowth and synapse formation have been studied in some detail, comparably little is known about the mechanisms underlying pruning. In holometabolous insects, pruning occurs at large scale during metamorphosis to remove larval-specific neurites. In the peripheral nervous system (PNS) of Drosophila, the so-called class IV dendritic arborization (c4da) neurons specifically prune their long and branched larval dendrites at the onset of the pupal phase by a degenerative mechanism [3,4]. C4da neuron dendrite pruning is induced by a prepupal peak in the steroid hormone ecdysone [3,4]. Ecdysone acts cell-autonomously in c4da neurons by inducing the expression of pruning genes such as the transcription factor Sox14 and the actin-severing enzyme Mical [5], an oxidoreductase that can sever actin filaments through actin oxidation [6], as well as the putative growth regulator headcase [7]. The first morphological signs of dendrite pruning are seen at around 3-5 h after puparium formation (h APF), when dendrites start to show local thinnings and varicosities in their proximal regions that appear to be due to changes in cytoskeletal and membrane stability. At these proximal sites, the dendrites are eventually severed between 6 and 12 h APF. Known pathways that contribute to this destabilization of the proximal dendrites are local microtubule disassembly [4,8,9] and alterations in plasma membrane trafficking [10][11][12][13]. Microtubule disassembly is induced by a signal transduction cascade involving the kinase Par-1 which negatively regulates the microtubule-associated protein tau to enhance microtubule dynamics [9]. Loss of microtubules starts at proximal dendrite branchpoints and proceeds with a proximal-to-distal directionality [14]. Dendritic microtubules display a uniform plus end-in orientation, and this uniformity is required for dendrite pruning [14]. Together with the observed directionality of microtubule breakdown, this indicates that microtubule breakdown occurs mostly from plus ends during dendrite pruning and that microtubule polarity acts as a spatial determinant [15]. Once severed, pruned dendrites are subsequently fragmented in a caspase-dependent manner and phagocytosed by epidermal cells [16,17].
While the roles and importance of microtubule regulation during pruning are emerging, relatively little is known about actin regulation during the process. While it is clear that the actin-severing enzyme Mical is induced in c4da neurons at the onset of the pupal stage and is required for dendrite pruning [5], it is not known whether it affects actin structures at this stage, and whether other actin regulators are involved in dendrite pruning. This is somewhat surprising because actin dynamics play important roles during earlier larval c4da neuron dendrite development. For example, Arp2/3-dependent actin polymerization promotes dendrite branching [18], and this also requires the actin disassembly factor cofilin to increase actin dynamics [19]. One factor that has recently been implicated in actin regulation during larval c4da neuron dendrite development is Widerborst (Wdb), encoding a regulatory B subunit of protein phosphatase 2A (PP2A) [20]. PP2A is known to regulate both microtubules, e.g., through tau [21], and actin, e.g., through Rho GTPases or regulators of cortical actin [22,23]. It is a trimeric protein complex consisting of an A subunit that acts as a scaffold (encoded by PP2A-29B in flies), a C subunit containing the active site (encoded by microtubule star/mts), and one of several regulatory B subunits. In addition to Wdb, the B subunit Twins (Tws) has also been linked to actin regulation during imaginal disk development [24].
In this study, we identify PP2A as a regulator of c4da neuron dendrite pruning. In a survey of phosphoregulators of dendrite pruning, we found that loss of the scaffold subunit PP2A-29B caused strong dendrite pruning defects. The catalytic subunit mts and-in a somewhat redundant manner, the B subunits Wdb and Tws are also required for this process, indicating the involvement of a specific PP2A holoenzyme. During dendrite pruning, PP2A displays genetic interactions with Mical, the actin disassembly factor cofilin and other actin regulators, indicating that PP2A acts via regulated actin disassembly during the process.

Results
The serine/threonine phosphatase PP2A is required for c4da neuron dendrite pruning In order to identify phosphoregulators of c4da neuron dendrite pruning, we expressed dsRNA constructs targeting signaling molecules under the control of the c4da neuron-specific GAL4 driver ppk-GAL4 and visualized c4da neurons by coexpression of membrane-bound GFP. Control c4da neurons expressing Orco dsRNA (against Odorant receptor co-receptor which is not expressed in c4da neurons) have long and branched dendrites at the thirdinstar larval stage (Fig 1A), which are completely and specifically pruned at 18 h APF (Fig 1A', G, and H). Loss of PP2A-29B, encoding the A subunit of the serine/threonine phosphatase PP2A, or the catalytic C subunit encoded by Microtubule star (mts), caused a decrease in branching and dendritic field coverage at the third-instar larval stage (Figs 1B-F and EV1). At 18 h APF, PP2A-29B knockdown caused dendrite pruning defects (Fig 1B'). This phenotype was highly penetrant, as most c4da neurons showed pruning defects at this stage (Fig 1G), and also very severe, as most neurons retained many primary and secondary dendrites still attached to the soma ( Fig 1H). In order to confirm this result, we next used Mosaic Analysis with a Repressible Cell Marker (MARCM) [25] to generate homozygous PP2A-29B mutant c4da neurons. C4da neurons homozygous for the loss-of-function allele PP2A-29B GE16781 also displayed dendrite pruning defects at 18 h APF (Fig 1C', G, and H). Furthermore, these pruning defects could be rescued by GAL4/UASmediated expression of HA-tagged PP2A-29B in the MARCM clones (Fig 1D', G, and H).
In order to assess the requirement for PP2A catalytic activity, we next expressed a dominant-negative version of the catalytic subunit, dnMts, in c4da neurons. Similar to the effects of PP2A-29B downregulation, the expression of dnMts caused strong and penetrant dendrite pruning defects at 18 h APF (Fig 1E, E', G, and H). In order to confirm this result, we again used MARCM to create c4da neurons homozygous for mts s5286 , a P element insertion in the Mts gene. These c4da neurons also displayed strong dendrite pruning defects (Fig 1F-H).
In order to test which B subunit might be involved in the regulation of c4da neuron dendrite pruning, we used sgRNAs or dsRNA constructs for tissue-specific CRISPR and/or RNAi, as well as mutant analyses. The four B/B' subunits in the fly genome are encoded by Twins (Tws), PR72/CG4733, Well rounded (Wrd), and Widerborst (Wdb). While the expression of an sgRNA construct directed against CG4733 under ppk-GAL4 did not cause dendrite pruning defects at 18 h APF, an sgRNA construct against Tws resulted in mild pruning defects (Fig EV2A-D). The expression of a dsRNA construct against Wrd did not cause significant dendrite pruning defects (Fig EV2F), while the expression of a dsRNA construct against Tws again caused very mild defects (Fig EV2G and  J). In order to manipulate Widerborst, we used the mutant allele wdb 14 for MARCM analysis. Homozygous wdb 14 c4da neuron MARCM clones displayed clear dendrite pruning defects ( Fig EV2H). However, the penetrance of these defects was still lower than expected from the very strong defects caused by manipulation of PP2A-29B or Mts. PP2A B subunits can sometimes act in a redundant manner [26]. To address this possibility, we expressed Tws dsRNA in c4da neurons in a wdb 14 /+ heterozygous mutant background. This manipulation caused stronger dendrite pruning defects more similar to those caused by loss of PP2A-29B or Mts ( Fig EV2I  and J), indicating that these two B subunits can regulate pruning redundantly. Taken together, our data indicate that a PP2A holoenzyme complex is required for c4da neuron dendrite pruning.
PP2A does not interact with the Par-1/tau microtubule pathway during dendrite pruning We next asked how PP2A could regulate dendrite pruning. Because the role of PP2A in cytoskeleton regulation is well established, we wanted to assess a potential role for PP2A in microtubule disassembly. To this end, we expressed PP2A-29B dsRNA in c4da neurons and tested whether upregulation of the microtubule disassembly pathway(s) involved in dendrite pruning could ameliorate the dendrite pruning defects caused by this treatment. Tau heterozygosity or overexpression of Par-1 or kat-60L1 did not cause dendrite pruning defects by themselves (Fig EV3A-E). We next assessed whether these manipulations suppressed the pruning defects induced by PP2A downregulation. In order to control for potential UAS titration effects, we compared the effects of PAR-1 and kat-60L1 overexpression to overexpression of lacZ. However, none of the microtubule manipulations suppressed the pruning defects induced by loss of PP2A-29B (Fig EV3F-J), suggesting that the function of PP2A during c4da neuron dendrite pruning is not linked to Par-1/tau-mediated microtubule regulation.
The pruning defects caused by loss of PP2A also seemed qualitatively different from the defects caused by loss of PAR-1. Pruning dendrites of control c4da neurons develop varicosities as a sign of degeneration during the early pruning stages between approximately 3 h APF and 12 h APF [10]. These varicosities are round, occur in thinned regions of (proximal) dendrites, and are usually smaller than 5 lm in diameter. In contrast, unpruned c4da neuron dendrites expressing PP2A-29B dsRNA displayed varicosities at 18 h APF that were larger and often occurred at distal dendrite tips. Sometimes, they developed small filopodia-like protrusions (e.g., Fig EV4C), somewhat reminiscent of axonal growth cones, and these varicosities also were positive for the actin marker lifeact::GFP [27]. In unpruned dendrites of c4da neurons lacking PAR-1, only small, proximal varicosities could be seen that were reminiscent of the ones normally occurring in earlier (Fig EV4A-D, arrow in Fig EV4B).

PP2A interacts genetically with ecdysone target genes
During c4da neuron dendrite pruning, the steroid hormone ecdysone induces the expression of important pruning genes, in particular the transcription factor Sox14 and the actin-severing enzyme Mical. We therefore tested next whether Sox14 or Mical might interact with PP2A during dendrite pruning. Overexpression of Sox14 or Mical alone did not cause dendrite pruning defects (Fig 2A-C). However, Sox14 overexpression significantly reduced the severity of the dendrite pruning defects induced by loss of PP2A-29B, as assessed by the reduced number of dendrites attached to the soma under these conditions (Fig 2F, G, K, and L). Mical overexpression caused a significant reduction in both penetrance and severity of the pruning defects caused by PP2A-29B knockdown (Fig 2H, K, and L). In order to address whether actin-related domains of Mical, such as the oxidoreductase domain and the calponin homology (CH) domain, a putative actin binding site [28], are required for this genetic interaction, we next tested whether the expression of Mical mutants lacking these domains could also suppress the dendrite pruning defects induced by PP2A-29B knockdown. Overexpression of MicalDredox alone in c4da neurons did not cause dendrite dsRNA strongly enhanced the severity of the dendrite pruning defects (Fig 2J-L). While Mical overexpression strongly suppressed the pruning defects caused by loss of PP2A, it did not significantly affect the larval dendrite defects (Fig EV1), suggesting that the mechanistic basis underlying these defects may not be identical. Taken together, these data indicate that the role of PP2A during dendrite pruning is linked to the ecdysone targets Sox14 and Mical, and the actin-modifying domains of Mical are crucial for this.

Effects of PP2A on Sox14 and Mical expression
Sox14 and Mical are both transcriptionally induced by the ecdysone receptor at the onset of the pupal stage [5]. The observed genetic interactions between PP2A and these two factors could therefore reflect a defect in Sox14 and/or Mical expression (and hence a defect in ecdysone-mediated gene expression). To address this possibility, we next assessed the effects of PP2A knockdown on Sox14 and Mical expression by immunofluorescence. At 2 h APF, Sox14 can be detected in the nucleus of control c4da neurons ( Fig 3A). In order to downregulate PP2A, we next expressed either PP2A-29B dsRNA or dominant-negative Mts in c4da neurons and assessed the effects on Sox14 expression. While PP2A-29B knockdown did not affect Sox14 expression (Fig 3B and D), Sox14 levels seemed to be increased upon dnMts expression (Fig 3C and D). At 2 h APF, Mical is also robustly expressed in c4da neurons and localizes to the cytoplasm (Fig 3E). Mical was also normally expressed in neurons expressing PP2A-29B dsRNA (Fig 3F and J). Surprisingly, many c4da neurons expressing dnMts showed strongly reduced Mical staining at this stage (Fig 3G and J). To address these potentially contradictory results, we reassessed Mical expression at the white pupal stage (0 h APF). At this stage, c4da neurons expressing PP2A-29B dsRNA also displayed reduced Mical levels ( Fig 3H-J). We interpret these data as indicating a 2-h delay in Mical expression upon PP2A downregulation. However, dendrite severing and pruning take place between 5 h APF and 10 h APF. We assess pruning phenotypes at 18 h APF, and the pruning defects induced by PP2A-29B knockdown are still highly penetrant and severe at this much later stage. We therefore conclude that the observed genetic interactions between PP2A and Sox14/Mical cannot be explained through a role of PP2A in Mical gene expression alone.

PP2A-linked pruning defects can be suppressed by cofilin overexpression
The observation that PP2A interacts with Mical during dendrite pruning prompted us to investigate whether PP2A could be linked to actin regulation during this process. We therefore asked whether upregulation of a different actin-severing activity could also suppress the pruning defects caused by loss of PP2A. Cofilin is a well-characterized actin depolymerization factor that can also functionally cooperate with Mical [29]. We first asked whether Drosophila cofilin, encoded by Twinstar (tsr), was itself required for c4da neuron dendrite pruning. MARCM clones homozygous for the cofilin mutant allele tsr N121 did not display dendrite pruning defects at 18 h APF (Fig EV5A). However, tsr overexpression caused a partial suppression of the pruning defects upon PP2A-29B knockdown compared to the lacZ titration control (Fig 4A, D, E, H, and I).
Cofilin is inhibited by phosphorylation by LIM kinase [30,31] and activated through dephosphorylation by slingshot phosphatases [32], and this is important for neuronal morphogenesis [33]. Consequently, nonphosphorylatable versions of tsr are constitutively active, and phosphomimetic tsr mutant versions are inactive. Overexpression of UAS transgenes encoding nonphosphorylatable tsr S3A or phosphomimetic tsr S3E alone did not cause dendrite pruning defects (Fig 4B and C). UAS-tsr S3A afforded a similar, but not better, suppression of the pruning defects induced by PP2A knockdown as UAS-tsr wt (Fig 4F, H, and I), indicating that the phosphorylation state of cofilin does not affect its ability to suppress PP2A. UAStsr S3E enhanced the severity of the pruning defects upon PP2A knockdown, consistent with a mild dominant or synergistic effect (Fig 4G-I).
We also wished to assess the localization of cofilin in c4da neurons. To this end, we used transgenic N-terminally GFP-tagged Drosophila tsr driven by the GAL4/UAS system (UAS-GFP::tsr). GFP::tsr localized to multiple punctate, sometimes elongated structures in the soma and dendrites of c4da neurons during the larval stage (Figs 4J and M, and EV5). These GFP::tsr punctae were reminiscent of cofilin/actin aggregates that can be induced by cofilin overexpression or stress in mammalian cells [34]. In support of the idea that these punctae contained actin, GFP::tsr also strongly localized to the dendritic "spikes" on the dendrites of c3da neurons that are known to be actin-rich [35] (Fig EV5D) (the ppk-GAL4 insertion used for GFP::tsr expression in these experiments is also stochastically expressed in c3da neurons). At 6 h APF, most GFP::tsr punctae in c4da neurons had vanished and GFP::tsr now displayed a largely dispersed distribution (Fig 4J' and M). Notably, one or two bright elongated GFP::tsr accumulations could still be seen at this stage that localized proximally to dendritic thinnings in primary dendrites (Fig 4J'). This localization was somewhat reminiscent of the localization of active cofilin in filopodia [36]. C4da neurons expressing Mical dsRNA had a similar number of GFP::tsr punctae as control neurons at the larval stage (Fig 4K and M). However, several c4da neurons expressing Mical dsRNA still displayed many GFP::tsr accumulations at 6 h APF (Fig 4K' and M), indicating that Mical was required for the observed changes in GFP::tsr localization between larvae and pupae. In contrast to control neurons, GFP::tsr was evenly dispersed in larval c4da neurons expressing PP2A-29B dsRNA, with no punctae visible (Fig 4L and M). At 6 h APF, such GFP::tsr accumulations were also not seen at the bases of proximal dendrites in these neurons (Fig 4L' and M). Thus, PP2A interacts genetically with actin disassembly factors and affects the localization of cofilin in c4da neurons.

Loss of PP2A can be ameliorated by manipulation of actin regulators
In order to deepen the links between PP2A and actin regulation during dendrite pruning, we next sought to identify additional genetic interactions between PP2A and actin. To this end, we 4 of 12 EMBO reports 21: e48870 | 2020 ª 2020 The Authors downregulated known actin regulators and asked whether this could ameliorate the pruning defects caused by loss of PP2A. As a control, we expressed GFP::tsr in this background. While GFP::tsr did not reduce the penetrance of the pruning defects induced by PP2A-29 dsRNA, when compared to overexpression of tdTomato, it decreased their severity (Fig 5A, B, I, and J). This suppression was lower than with untagged tsr, but this could be due to lower expression levels of GFP::tsr (this construct is a site-directed transgene which in our experience has lower expression when compared to randomly inserted ones    significantly, such that each neuron had fewer dendrite branches attached to the soma at 18 h APF (Fig 5C, D, I, and J). In order to manipulate additional regulators of actin polymerization, we next used mutants or dsRNA constructs. Partial loss of the actin polymerase enabled in a heterozygous ena 210 /+ mutant background did not have an effect on the severity of the pruning defects (Fig 5E, I, and J). Downregulation of profilin, an actin binding protein involved in the regulation of actin dynamics, significantly reduced the effects of PP2A-29B dsRNA when compared to an Orco control dsRNA (Fig 5F, G, I, and J). The strongest suppression of the severity of the pruning defects was achieved by downregulation of the cortical actin regulator moesin (Fig 5H-J).  We also performed an overexpression survey to identify possible kinases counteracting PP2A. While overexpression of LIM kinase, active atypical protein kinase C (aPKC), or abelson kinase (abl, a tyrosine kinase), did not cause dendrite pruning defects, overexpression of a constitutively active form of protein kinase A (PKA mc*) caused strong and fully penetrant c4da neuron dendrite pruning defects (Fig EV6). However, neither inhibition of PKA nor the previously identified negative pruning regulator TOR [37] could suppress the pruning defects caused by PP2A knockdown (Fig EV6).

A B C D
Taken together, our results suggest that PP2A regulates one or several aspects of actin dynamics and/or cortical actin organization that are required for dendrite pruning.

Discussion
In this study, we identified an important role for the protein phosphatase PP2A during large-scale dendrite pruning of Drosophila c4da neurons during metamorphosis. Our data indicate that a PP2A holoenzyme containing either the Wdb or Tws regulatory subunit is involved in pruning regulation. Our data strongly link PP2A to actin regulation during dendrite pruning. In particular, our genetic interaction studies show that the pruning defects caused by loss of PP2A can be suppressed by overexpression of the actin-severing enzyme Mical. Mical is induced by ecdysone at the onset of the pupal stage and is required for c4da neuron dendrite pruning. While our data and an accompanying study by Yu and colleagues [38] show that induction of Mical expression is delayed by loss of PP2A, this effect is transient, and there is no strong effect on Mical expression at 2 h APF, when other mutants that directly affect Mical expression still show strongly reduced Mical levels (e.g., Ref. [39,40]). While the delay in Mical expression could contribute to the observed pruning defects, several lines of evidence indicate that PP2A has an additional function in actin regulation, such as the observations that the actin-related domains of Mical are required for suppression of the PP2A phenotype (Fig 2) and that overexpression of cofilin can also partially rescue the PP2A phenotype (Fig 4). Furthermore, our genetic analyses (Fig 5) link PP2A to actin dynamics and cortical actin organization. In this context, it is interesting that c4da neurons lacking PP2A had an altered distribution of GFP::tsr (GFP-tagged cofilin) (Fig 4). This transgene localized to punctate structures upon GAL4-mediated expression. It is known that active cofilin can coassemble with actin into so-called cofilin rods that resemble actin/ cofilin structures at the base of filopodia where actin turnover is high [36]. As GFP::tsr also localizes to the actin-rich dendritic spikes of c3da neurons (Fig EV5), it is interesting to speculate that the formation of these structures may in part reflect the overall F-actin amount in the cell, or a cell's propensity to form F-actin. The lack of GFP::tsr punctae in c4da neurons lacking PP2A might therefore indicate globally altered actin dynamics (Fig 4). These results will be important leads in order to better define the role of PP2A and actin regulation during dendrite pruning in the future. Since the data presented by us and others [23,24] suggest that loss of PP2A affects actin dynamics and hence possibly both F-actin assembly and disassembly, it is interesting to speculate that the underlying causes for the larval dendrite morphogenesis defects and the pruning defects may be similar. We therefore tentatively place PP2A in a pathway at least partially in parallel to Mical during dendrite pruning (Fig 6).
While our genetic data suggest that PP2A is not involved in the temporal regulation of microtubule disassembly via the Par-1/tau pathway (Fig EV3), the parallel study by the Yu lab [38] found that loss of PP2A leads to a defect in dendritic microtubule orientation. We have previously found that the uniform plus end-in orientation of dendritic microtubules is required for dendrite pruning [14]. It is therefore conceivable that these microtubule-based defects also contribute to the observed dendrite pruning defects. Which of the observed defects in gene expression, microtubule orientation and actin dynamics contributes most to the observed defects remains to be seen. However, the combination of the two studies clearly establishes PP2A as a broad and important regulator of the neuronal cytoskeleton during development.
Cloning and transgenes HA PP2A-29B and GFP::tsr were cloned into pUAST attB by standard methods. Transgenes were injected in flies carrying the 86Fb acceptor site [53].

Dissection, microscopy, and live imaging
For analysis of pruning defects, pupae were dissected out of the pupal case at 18 h APF and analyzed live using a Zeiss LSM 710 confocal microscope. For PP2A-29B genetic interactions, candidate modifiers were crossed to a second chromosome insertion of ppk-GAL4 combined with UAS-CD8GFP and UAS-dicer2 and UAS-PP2A-29B dsRNA on the third chromosome (BL# 29384). UAS-GFP::tsr was expressed under ppk-GAL4 and imaged live in ether-anaesthetized third-instar larvae or at 6 h APF. All images were analyzed using Fiji [54].

Antibodies and immunohistochemistry
Pupal body wall filets were dissected quickly in PBS and fixed in PBS containing 4% formaldehyde for 20 minutes. Chicken anti-GFP antibodies were from Aves labs, respectively. Other antibodies were guinea pig anti-Sox14 [55] and rabbit anti-Mical [40].

Quantification and statistical analysis
Pruning phenotypes in Figs 1, 2, 4, and 5 were analyzed by determining the fraction of neurons that still had dendrites attached to the soma to reflect the phenotypic penetrance, and these data were analyzed using a two-tailed Fisher's exact test. To assess severity, we also counted the number of primary and secondary branches (i.e., the sum of all primary and secondary dendrites per neuron) still attached to the soma at 18 h APF. These data were analyzed using Wilcoxon's test. In a similar way, we determined the number of neurons with unusual varicosities in Fig 5A-C. For quantification of immunofluorescence experiments, c4da neuron staining intensities were measured in Fiji and normalized to c1da neuron staining intensities in the same image. These data were analyzed using Wilcoxon's test.
The number of GFP::tsr punctae was mean AE s.d. and analyzed using Wilcoxon's test. For dendritic field coverage analysis, dendritic fields were defined by segment border denticles (in the anterior/posterior direction), the dorsal midline, and the middle between dorsal and lateroventral c4da neuron dendrites (in the dorsoventral direction). Actual coverage was calculated by actin disassembly

PP2A
? ? dendrite pruning Our data indicate a two-pronged effect of PP2A on pruning: firstly, PP2A is required for timely expression of Mical via an unknown mechanism. Secondly, PP2A appears to affect actin dynamics in neurons during both the larval and pupal stages.
10 of 12 EMBO reports 21: e48870 | 2020 ª 2020 The Authors connecting outer dendrite terminals with each other as in Ref. [35]. The covered area was then compared to the maximal dendritic field.
Expanded View for this article is available online.