Optic tectal superficial interneurons detect motion in larval zebrafish
- 429 Downloads
Detection of moving objects is an essential skill for animals to hunt prey, recognize conspecifics and avoid predators. The zebrafish, as a vertebrate model, primarily uses its elaborate visual system to distinguish moving objects against background scenes. The optic tectum (OT) receives and integrates inputs from various types of retinal ganglion cells (RGCs), including direction-selective (DS) RGCs and size-selective RGCs, and is required for both prey capture and predator avoidance. However, it remains largely unknown how motion information is processed within the OT. Here we performed in vivo whole-cell recording and calcium imaging to investigate the role of superficial interneurons (SINs), a specific type of optic tectal neurons, in motion detection of larval zebrafish. SINs mainly receive excitatory synaptic inputs, exhibit transient ON- or OFF-type of responses evoked by light flashes, and possess a large receptive field (RF). One fifth of SINs are DS and classified into two subsets with separate preferred directions. Furthermore, SINs show size-dependent responses to moving dots. They are efficiently activated by moving objects but not static ones, capable of showing sustained responses to moving objects and having less visual adaptation than periventricular neurons (PVNs), the principal tectal cells. Behaviorally, ablation of SINs impairs prey capture, which requires local motion detection, but not global looming-evoked escape. Finally, starvation enhances the gain of SINs’ motion responses while maintaining their size tuning and DS. These results indicate that SINs serve as a motion detector for sensing and localizing sized moving objects in the visual field.
Keywordsoptic tectum motion detection direction selectivity visual adaptation zebrafish
Animals distinguish prey, conspecifics and predators from the constantly changing world through combing a number of objective features, among which motion is an essential one (Mauss et al., 2017). In visual areas of the brain, local circuits integrate visual inputs to represent motion information. The optic tectum (OT), the visual center in low vertebrates and the homolog of the superior colliculus in mammals, is the primary target of RGC axon terminals and transmits behavior-relevant information down to motor outputs, which orient the body axis toward or away from perceived objects (Dunn et al., 2016; Gahtan et al., 2005; Nevin et al., 2010). Thus, the processing of motion information within the OT is instrumental to object monitoring and visuomotor transformation. With regard to motion detection, an important feature that can be extracted is the direction of a moving object. Different cell types within the retina have been characterized to be tuned to motion directions (Barlow and Hill, 1963; Kim et al., 2008; Oyster and Barlow, 1967; Vaney et al., 2012; Wyatt and Daw, 1975). In zebrafish, different subtypes of DS-RGCs and orientation-selective (OS) RGCs were also identified (Nikolaou et al., 2012). Beyond the retina, downstream DS cells, especially distinct neuronal subtypes within the OT are just beginning to be characterized (Grama and Engert, 2012; Hunter et al., 2013; Niell and Smith, 2005). Specifically, two subtypes of GABAergic DS cells were identified with a matching laminar distribution of DS-RGC inputs (Gabriel et al., 2012). In addition to directional information, RGCs also encode size information for moving objects, endowing the animal the ability to localize and distinguish sized local objects (Preuss et al., 2014). Ethologically, motion information provides essential cues to signal physiological meaning such as food resources and threatening and thus is under elaborate processing (Borst and Euler, 2011).
Resided in the input layer of the tectal neuropil, superficial interneurons (SINs), a population of GABAergic interneurons, were reported to be involved in prey capture (Del Bene et al., 2010). However, the functional properties of SINs specialized for specific visuomotor behaviors remain poorly understood. Here, we address this question by using in vivo whole-cell recording and functional calcium imaging in larval zebrafish. We identified two subsets of DS SINs with preferred directions separated by ∼120° and approximately cover rostral to caudal (RC) directional information separated by ∼120° SINs exhibit sustained high frequency firing with current injection, transient ON- and OFF-type light responses, large RF consistent with their broadly stratified arborization, and mainly receive excitatory inputs. SINs show size-dependent responses to moving dots. Further characterization reveals that SINs are activated by a moving object but not a static one and capable of showing sustained responses to a moving object within the RF, which could be explained by less visual adaptation to paired-pulse stimuli than that of periventricular neurons (PVNs). Behaviorally, ablation of SINs impairs prey capture which requires fine local motion detection but not global looming-evoked fast escape. In addition, motion responses of SINs show gain modulation by feeding state, in which starvation increases response amplitude and ratio of responsive cells while maintaining size tuning and DS properties.
Electrophysiological properties of SINs
To directly investigate SIN visual functions, whole-field dimming stimulation was imposed to the larva. The majority of SINs showed transient ON and OFF responses (84%; n = 77/92) while the rest showed only transient OFF responses (16%; n = 15/92; Fig. 1D). To compare excitatory and inhibitory inputs, diming stimulation evoked responses at different holding potentials were temporally divided into two synaptic components after stimulation onset (Fig. 1E). The early component (42 ± 1 ms to 82 ± 10 ms after stimulation onset) was large and reversed at ~0 mV, suggesting strong excitatory inputs from RGCs. Meanwhile, the late component (127 ± 24 ms to 168 ± 32 ms after stimulation onset) was weak and reversed at ~−60 mV, equal to the reversal potential of chloride currents(~−60 mV), suggesting weak or absence of inhibitory inputs (Fig. 1F). We calculated evoked conductance from linear regression over a fixed voltage range from −80 to −20 mV to avoid the sublinear behavior at the extremes of the I–V relationship. The ratio of excitatory conductance (0.51 ± 0.09 nS) to inhibitory conductance (0.2 ± 0.03 nS) was 2.6, suggesting inputs to SINs are dominated by barrages of excitation. We next mapped the RF properties of SINs, which reflect the spatial arrangement of inputs and support fundamental visual functions (Figs. 1G, S1C and S1D). The RF size was quantified as the average of the half width at half maximal from the two axis of the ellipse that was fitted from a 2D Gaussian model. SINs had large spatial RF size of 37° ± 3° in average. In addition, we found that the averaged RF size in the horizontal axis (49° ± 6°) is significantly larger than that in the vertical axis (25° ± 3°; Fig. 1H), which reflects more coverage and intense information processing of the horizontal field.
A proportion of SINs are direction selective
SINs are size-tuned to moving objects
Then we asked how PVNs, the potential downstream tectal cells, respond to moving dots with different sizes. To this end, we measured the size tuning property of PVNs with Tg(HuC:GCaMP5) line, which expresses GCaMP5 pan-neuronally (Fig. 3D). The distribution of preferred sizes of individual PVNs revealed a maximal preference of 20 degree (Fig. 3E and 3F). A direct comparison of the tuning curves between SINs and PVNs revealed sharpened tuning for PVNs, in which local SIN inhibitory input is likely to play a role (Fig. 3G).
SINs detect and show sustained responses to moving objects
SINs are crucial for prey capture but not escape
Brain state-dependent gain modulation of motion detection of SINs
In the present study, we provide direct evidence for motion detection properties of SINs within the tectum. As SINs are located at the most superficial neuropil layer where RGC afferents terminate, it is probable that SINs themselves receive only RGC excitatory inputs. While the negligible inhibitory inputs evoked by dimming stimulation may result from potential mutual inhibition among SINs.
By combining the merits of GCaMP-HS, an improved version of calcium indicator, and behaviorally relevant visual stimuli, our results demonstrate that SINs respond robustly to 10° moving bars and moving dots of various sizes. The observation of the tuning properties of the two populations of DS SINs is supported by the result from OGB-labeled superficial neuropil cells (Hunter et al., 2013), although a minor population of SINs that prefer caudal-to-rostral motion were reported (Abbas et al., 2017). SIN’s DS may directly derive from the subset of DS-RGCs, thus enabling SINs specialized for detecting motion along the horizontal axis of the visual field. The stronger RC inhibition derived from SINs, together with relatively strong CR-tuned retinal input to the tectum (Maximov et al., 2005; Nikolaou et al., 2012), may contribute to the prevalence of CR-tuned tectal cells. In the tectal cell body region, two DS subtypes were identified with opposite preferred directions in the horizontal axis (Gabriel et al., 2012). Except for potential mutual inhibition under competing stimuli (Mysore and Knudsen, 2012, 2013), SINs may provide null direction inhibition observed in the CR-tuned DS type. This form of feedforward null-direction inhibition could contribute to fine-tuning the turning angle of an orienting swim. Collectively, these distinct cell types tuned to directional motion endow the tectum and the superior colliculus the functional role in directing eye-head-body movements toward or away from a moving object (Gandhi and Katnani, 2011).
PVNs were reported to show negative spatial summation, wherein neurons have RF size larger than their preferred size (Niell and Smith, 2005). Comparing the tuning curves of SINs and PVNs, it’s probable that large size tuned SINs provide local inhibition that underlies the negative spatial summation in PVNs. Similar to SINs, somatostatin-positive inhibitory neurons (SOMs) in the superficial layers of the mouse visual cortex exhibit increasing responses with stimulation of the RF surround and contribute to pyramidal cells’ surround suppression (Adesnik et al., 2012; Barker and Baier, 2013). Distinct size discrimination properties therefore comprise a functional module within the tectum that distinguishes differentially sized objects with ethological meanings.
If one neuron is sensitive to motion, then it’s intriguing to know whether it keeps the motion information or only show transient response profile. Our finding that SINs are motion sensitive and show sustained response provides a substrate for maintaining local motion information and allowing the tectum to assemble a representation of the overall pattern of motion in the environment for execution of distinct, ethologically relevant behaviors (Silies et al., 2014). Correspondingly, functional imaging showed that tectal neurons of larval zebrafish responded robustly to a paramecium when it started swimming but not staying still in the visual field (Muto et al., 2013).
Ablation of SINs impaired zebrafish visually guided prey capture behavior but not global looming evoked fast escape, indicating the important role of localization of fine local objects by SINs and possible mechanism of compensation or redundancy for representation of global motion by the tectal circuit. To be mentioned, our ablation manipulation was based on the Gal4 enhancer trap line which labels only a fraction of SINs. Thus we do not exclude the possibility that the whole SIN population may also play a role in fast escape evoked by looming stimuli (Dunn et al., 2016) or affect avoidance response to a moving dot a little bit larger than the size of a paramecium, which could evoke avoidance behavior (Bianco et al., 2011; Trivedi and Bollmann, 2013).
Sensory processing is strongly influenced by brain state, in which starvation positively or negatively modulates neural activities in olfactory, gustatory and visual systems across animal species according to feeding requirement and limited energy allocation (de Araujo et al., 2006; Longden et al., 2014; Marella et al., 2012; Pager et al., 1972; Root et al., 2011). The modification of response gain of SINs in different feeding states may result from neuromodulation originated from the hypothalamic-pituitary-adrenal axis (Filosa et al., 2016) and further contribute to visual size discrimination in zebrafish under behavioral choices.
Future studies are required to probe the connectivity patterns among SINs and other cell types both at the upstream and downstream and how SINs directly involve in the local circuit. In conclusion, our results coherently demonstrate that SINs serve as motion detectors for extracting local spatial displacement feature derived from environmental moving objects, which underlies the important role of the tectum or the superior colliculus in appropriate behavioral choices among vertebrate species.
MATERIALS AND METHODS
Adult zebrafish (Danio rerio) were maintained in the National Zebrafish Resources of China (Shanghai, China) with an automatic fish-housing system (ESEN, China) at 28 °C following standard protocols (Mu et al., 2012; Wei et al., 2012). Electrophysiological recording and calcium imaging were performed on 7–8 days post fertilization (dpf) of larval zebrafish. All zebrafish handling procedures followed the Animal Use Committee of Institute of Neuroscience, Chinese Academy of Sciences.
Paramecium prey capture test
Zebrafish larvae were placed in a 24-well plate individually with 1.5 mL of paramecium solution containing approximately 15 paramecia per 200 μL. Intact control, ablated fish and blank control were separated sequentially to minimize effect of paramecium concentration. After adding larvae to individual well, the 24-well plate was placed in 28 °C incubator four hour later. Thereafter, remaining paramecia were counted in 200 μL solution from the well twice under a stereomicroscope and quantified as the averaged number. All values were normalized to the average number of the well without larvae. Consumed paramecia were calculated by (100%-(normalized remaining paramecia)).
Escape behavior test
Larval behavior was monitored with an infrared-sensitive high-speed camera at 500 Hz (Redlake Motionscope M3, US). Each larva was placed in a 3.5-cm Petri dish and allowed to freely swim in the test arena for over 15 min before experiment for adaptation. The behavior of six larvae in six individual dishes was simultaneously recorded during an experiment. Eight trials with 5 min interval were performed to calculate the probability of escape behavior for each larva.
In vivo electrophysiological recording
Zebrafish larvae were first paralyzed with the neuromuscular junction blocker a-bungarotoxin (100 μg/ml, Sigma) for 10–15 min, and were then embedded in ~1.5% low melting agarose (Sigma) for mechanical fixation. The extracellular solution consisted of (in mmol/L): 134 NaCl, 2.9 KCl, 2.1 CaCl2, 1.2 MgCl2, 10 HEPES and 10 glucose (290 mOsm/L, pH = 7.8). In vivo whole-cell recording of SINs and PVNs were made under infra-red visual guidance through a tiny cut for breaking the skin made at the middle line. The recording pipette was pulled from borosilicate glass capillaries (BF100-58-10, WPI), had a resistance in the range of 15-20 MΩ, and was tip filled with internal solution and then backfilled with internal solution. The internal solution consisted of (in mmol/L): 110 K-gluconate, 10 KCl, 2 CaCl2, 2 Mg-ATP, 0.3 Na2-GTP, 10 HEPES, 10 EDTA and 10 phosphocreatine (280 mOsm/L, pH 7.4). Recording was made with a patch-clamp amplifier (MultiClamp 700B; Axon Instruments) and signals were filtered at 5 kHz and sampled at 10 kHz using AxoScope software 10.0 (Axon Instruments). The data were discarded if the series resistance varied by >20% during recording. All drugs were purchased from Sigma-Aldrich unless otherwise mentioned.
For calcium imaging of SINs, we used double transgenic zebrafish Tg(Gal4-1156t,UAS:GCaMP-HS) larvae that were obtained by crossing Tg(UAS:GCaMP-HS) (gift from Dr. Koichi Kawakami) with the Gal4 enhancer trap line Tg(Gal4-1156t) (ZIRC). Confocal calcium imaging was carried out under a 40×, 0.8 NA water-immersion objective using an Olympus Fluoview 1000 confocal microscope. A recording chamber was custom built with one side enclosed by a diffusive screen. The larva was mounted dorsal side up in ~1.5% agarose on the edge of a raised platform in the imaging chamber, allowing an unobstructed view of the projected stimuli on the screen of the chamber and positioned with the contralateral eye facing the projection area, which covered a visual field of approximately 110° by 110°.
Visual stimuli were programmed using custom-written software based on MATLAB (Mathworks) and the Psychophysics Toolbox (Brainard, 1997; Pelli, 1997) and presented with a micro-projector (ASK). A colored filter directly in front of the display was used to block green light, in order to prevent interference with the fluorescence emission of GCaMP-HS. To measure the spatial RF, a pseudo random sequence of single black squares (4 × 10°) was presented for 0.2 s with an interval of 0.2 s. To measure size tuning, the black dot of various sizes that were compensated for constant visual angles was moving at a speed of 30°/s. To measure direction selectivity, the black bar was 10° in width and moving at a speed of 30°/s, in eight directions evenly spanning 360°. To measure motion sensitivity, the black dot in 10° was moving at a speed of 30°/s, in four directions evenly spanning 360°. To measure sustained response to motion, the black dot in 10° was moving at a speed of 30°/s into the RF, rotating in a series of 5 speeds from 10 to 90°/s. To measure visual adaptation, whole-field dimming pair with a series of 5 intervals from 1 s to 9 s was presented for 0.5 s, respectively. To measure escape, looming stimulation was presented with a black circle appearing, smoothly expanding at a speed of 5.4 cm/s and finally covering the whole screen. Diming stimulation with 0.4 s duration was presented. All stimuli were presented on white background.
We quantified the spatial structure of neuronal RFs by using the average response in a manually selected window, which includes the largest variance, from the stimulation period. The 2D grid of neuronal membrane potentials was analyzed parametrically by fitting the response profile with a 2D Gaussian model (Womelsdorf et al., 2008). The PD and DSI were determined as the direction and magnitude of the vector sum of the averaged peak responses from three stimulus repetitions for each direction (Gabriel et al., 2012).
For independent data sets with only two groups we used the Student’s t-test or Wilcoxon rank-sum test, and for data from multiple groups we used the two-way ANOVA with mixed design or repeated measures to look for differences between factors. In data obtained from the same group under different conditions, the Paired-samples t-test or Wilcoxon signed-rank test was used. Differences were regarded as statistically significant at P-values of <0.05. All results are represented as mean ± SEM.
All data included in this study are available upon reasonable request from the corresponding author.
This work was supported by the Shanghai Science and Technology Committee (No. 18JC1410100, J. Du), Key Research Program of Frontier Sciences of Chinese Academy of Sciences (No. QYZDY-SSW-SMC028, J. Du), Strategic Priority Research Program of Chinese Academy of Sciences (No. XDBS01000000, J. Du), China Wan-Ren Program (J. Du), Shanghai Leading Scientist Program (J. Du). The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
CR, caudal to rostral; dpf, days post fertilization; DS, direction-selective; DSI, direction selectivity index, DV, dorsal to ventral; OSI, orientation selectivity index; OT, optic tectum; PD, preferred direction; PO, preferred orientation; PPR, paired-pulse ratio; PVNs, periventricular neurons; RC, rostral to caudal; RF, receptive field; RGCs, retinal ganglion cells; ROIs, region of interests; SINs, superficial interneurons; VD, ventral to dorsal
COMPLIANCE WITH ETHICS GUIDELINES
Chen Yin, Xiaoquan Li and Jiulin Du declare that they have no conflict of interest. All institutional and national guidelines for the care and use of laboratory animals were followed.
C. Yin and J. Du conceived the project and designed experiments; C. Yin and X. Li performed experiments; C. Yin analyzed data; C. Yin and J. Du wrote the paper.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.