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Insects are equipped with various types of antennal sensilla, which house thermosensitive neurons adapted to receive different parameters of the thermal environment for a variety of temperature-guided behaviors. In the leaf-cutting ant Atta vollenweideri, the physiology and the morphology of the thermosensitive sensillum coeloconicum (Sc) has been thoroughly investigated. However, the central projections of its receptor neurons are unknown. Here we selectively stained the three neurons found in single Sc and tracked their axons into the brain of Atta vollenweideri workers. Each of the three axons terminates in a single glomerulus of the antennal lobe (Sc-glomeruli). Two of the innervated glomeruli are adjacent to each other and are located laterally, while the third one is clearly separated and located medially in the antennal lobe. Using two-photon Ca2+ imaging of antennal lobe projection neurons, we studied where in the antennal lobe thermal information is represented. In the 11 investigated antennal lobes, we found up to 10 different glomeruli in a single specimen responding to temperature stimulation. Both, warm- and cold-sensitive glomeruli could be identified. The thermosensitive glomeruli were mainly located in the medial part of the antennal lobe. Based on the general representation of thermal information in the antennal lobe and functional data on the Sc-glomeruli we conclude that temperature stimuli received by Sc are processed in the medial of the three target glomeruli. The present study reveals an important role of the antennal lobe in temperature processing and links a specific thermosensitive neuron to its central target glomerulus.
Insects possess a highly developed thermal sense to assess various parameters of their thermal environment. Apart from temperature avoidance or preference required for successful thermoregulation of the own body temperature some insects utilize their thermal sense for amazingly sophisticated temperature-guided behaviors. For example blood-sucking bugs detect thermal radiation emitted by their endothermic prey to receive a blood meal (Lazzari and Núñez, 1989; Schmitz et al., 2000; Lazzari, 2009), Australian fire beetles locate forest fires to encounter mates and to reproduce (Evans, 1964; Vondran et al., 1995; Schmitz et al., 1997), and leaf-cutting ants can use thermal radiation as an orientation cue (Kleineidam et al., 2007). Most of the thermosensitive neurons that receive thermal information about the environment in insects are located on the antennae within cuticular structures termed peg-in-pit sensilla. These sensilla generally house three receptor neurons, combining one thermosensitive neuron with either two antagonistic hygrosensitive neurons (Waldow, 1970; Tichy, 1979; Altner et al., 1981; Altner and Loftus, 1985) or two chemosensitive neurons (Altner et al., 1977, 1981; Davis, 1977; Hansson et al., 1996). In social insects the thermo-hygrosensitive combination has been described for sensilla coelocapitula in the honeybee Apis mellifera (Yokohari, 1983). Other thermosensitive neurons have been found in sensilla ampullacea and the sensilla coeloconica (Lacher, 1964; Dumpert, 1978; Kleineidam and Tautz, 1996).
In the leaf-cutting ant Atta vollenweideri the sensilla coeloconica (Sc) have been studied in great detail. This sensillum is mainly located at the tip of the flagellum and has a remarkable peg-in-pit morphology where the sensory peg is deeply sunken in the cuticular pit, which is separated from the environment by a tiny aperture (Ruchty et al., 2009). The sensillum houses a thermosensitive (cold-sensitive) neuron presumably combined with two additional chemosensitive neurons (Ruchty et al., 2009). Recent electrophysiological investigations revealed an extreme sensitivity and high temporal resolution of the thermosensitive neuron (Ruchty et al., 2010). Based on the response characteristic to thermal stimuli and due to the extraordinary morphology of the sensillum, this neuron has been suggested as a candidate for detecting spatially distributed thermal objects during thermal landmark orientation (Kleineidam et al., 2007; Ruchty et al., 2009, 2010). In order to understand how insects orient in their thermal environment, it is necessary to know where and how thermal information is processed in the central nervous system. Until now, the central projections of thermosensitive neurons have been investigated only in a single study (Nishikawa et al., 1995). This tracing study nicely shows where thermal information of two specific thermosensitive neurons is further processed in the antennal lobe of the cockroach. However, it leaves unspecified where thermal information is represented within the whole antennal lobe volume.
In the present study we investigate the representation of thermal information in the antennal lobe of the leaf-cutting ant Atta vollenweideri. In particular, we focus on the thermal information received by the thermosensitive neuron of the Sc. Using two-photon Ca2+ imaging we measure the spatiotemporal neuronal activity upon temperature stimulation throughout the whole antennal lobe neuropil. By selectively staining single sensilla (Sc), we investigate the central projections of the receptor neuron axons into the ants’ antennal lobes (Sc target glomeruli). Based on the correlation between the representation of thermal information within the antennal lobe and the Sc target glomeruli, we identify the target glomerulus of the thermosensitive neuron of the Sc.
Workers of Atta vollenweideri were obtained from a laboratory colony collected in 2002 at the Reserva Ecológica El Bagual, Formosa, Argentina. The colony was reared at the Biozentrum of the University of Würzburg at 25°C and 50% relative humidity in a 12-h/12-h photoperiod, and fed mainly with leaves of privet (Ligustrum vulgaris) and dog rose (Rosa canina). The performed experiments comply with the current laws of the Federal Republic of Germany.
We selectively stained single sensilla coeloconica (Sc) (single-staining) and investigated the anterograde projection of the receptor neuron axons into the ants’ brains. Ants were mounted onto plexiglass holders with dental wax (surgident periphery wax, Heraeus Kulzer, Germany) and a strap of adhesive tape. Following the immobilization procedure, the scapus of each antenna was glued onto the holder by using white-out correction fluid (Tipp-Ex, Bic, France). Under visual control and at a magnification of 390× (Leitz microscope equipped with NPL-Fluotar L25/0.35, Leitz, Germany) an electrolytically sharpened tungsten electrode was inserted into a single Sc. The sensory peg was deliberately injured by carefully moving the electrode into the sensillum, which caused the permeation of receptor lymph into the chamber as observed under the microscope. The injured dendrites were then stained via a droplet of dextran–biotin (D-7135, Molecular Probes) dissolved in distilled water and applied onto the antennal tip for 10min using a Hamilton syringe.
To investigate whether the target region in the ant's brain was exclusively innervated by receptor neuron axons of the Sc, we carried out a double-staining experiment. Subsequently to the single-staining we extensively cut antennal hair sensilla with a razorblade and stained the dendrites with tetra-methyl-rhodamine-dextran+ biotin (3,000 MW, lysine-fixable; Microruby, D 7162, Molecular Probes) dissolved in distilled water.
All individuals from the single- and double-staining experiments were freed from the holders immediately after dye application and were kept separately in Petri dishes for the remaining staining period in order to avoid social grooming that could have decreased the staining success. After 24h, the brains of the ants were dissected under ant saline solution (127mM NaCl, 7mM KCl, 1.5mM CaCl2, 0.8mM Na2HPO4, 0.4mM KH2PO4, 4.8mM TES, 3.2mM Trehalose, pH 7.0), transferred into ice-cold fixative (4% formaldehyde in phosphate buffered saline [PBS], PH 7.2), and stored over night in the fridge. Brains were then rinsed in PBS (three times à 10min) and subsequently incubated in Alexa 488 conjugated streptavidin (S-11226, Molecular Probes, Eugene, OR) for 48h. After being rinsed again in PBS (three times à 10min), the brains were dehydrated in an ascending ethanol series (50, 70, 90, 95, and three times 100%, á 10min), transferred into methyl-salicylate (M-2047, Sigma-Aldrich, Steinheim, Germany), and finally investigated under a confocal-laser-scanning microscope (Leica TSC SP 2, Leica Microsystems, Wetzlar, Germany). The software AMIRA 3.1 (Mercury Computer Systems, Berlin, Germany) was used to analyze the confocal image stacks (resolution: x: 0.3μm; y: 0.3μm; z=1μm) and to reconstruct the innervated neuropils as well as the axons of the labeled receptor neurons.
In order to study where in the antennal lobe thermal information is represented, we used a staining technique, which was already successfully used for calcium imaging in honeybees (Sachse and Galizia, 2002) and ants (Zube et al., 2008; Dupuy et al., 2010). We retrogradely labeled projection neurons that connect the antennal lobe via two antenno-protocerebral tracts (APTs) to the mushroom bodies and the lateral horn (Mobbs, 1982; Kirschner et al., 2006; Galizia and Rössler, 2010). The selective staining of projection neurons results in an excellent signal to noise ratio for two-photon Ca2+ imaging. Single ants were mounted in plexiglass holders using dental wax (surgident periphery wax, Heraeus Kulzer, Germany). Subsequently a small window was cut into the head capsule, and tracheae, glands, and muscles were gently moved aside in order to access the dye injection site in the lateral protocerebrum, close to the vertical lobe (alpha-lobe) of the right mushroom body. Prior to the dye injection a sharp glass electrode was used to perforate this region and to injure the projection neurons of the APTs. Afterward a second glass electrode coated with some crystals of Fura-2 dextran (potassium salt, 10000 MW, F3029, Molecular Probes) dissolved in distilled water was inserted in the perforated region and remained there for approximately 10s. The brain was then covered by two-component glue (KWIK-SIL, World Precision Instruments, Berlin, Germany) to avoid desiccation, and the animals were kept in darkness for a staining period of around 3–4h. Prior to the functional imaging experiments we first detached the KWIK-SIL from the brain. Then glands, tracheae, and muscles covering the antennal lobe ipsilateral to the injection site were removed. Subsequently, we excised the esophagus at the mouthparts, pulled it for a few millimeters out of the head capsule and fixated it with some dental wax next to the head capsule. This procedure was done to reduce brain movement during data acquisition. In order to protect the preparation and the brain, we again covered it with KWIK-SIL before mounting the plexiglass holder with the ant at the imaging setup.
In vivo Ca2+ imaging was performed using a custom-built two-photon-laser-scanning microscope equipped with a Ti:sapphire laser system (MaiTai HP, Spectra-Physics, Newport, Santa Clara, USA) as light source (about 100fs output). To excite the Fura-2 dye we used a wavelength of 810nm. The laser intensity was adjusted with a Pockel's cell (Conoptics, Danburry, USA). The microscope was equipped with two galvanometric scan mirrors (Model 6210; Cambridge Technologies, Lexington, USA) for scanning the specimen in the x–y axis, and a piezoelectric focusing element (P-725.4CD PIFOC, Physik Instrumente, Karlsruhe, Germany) for z-scanning along the optical axis. A water immersion objective (25×; XPlan MP, 1.05 NA; Olympus) was mounted onto the piezo element, focusing the laser beam onto the antennal lobe and collecting the emitted fluorescence after dye excitation. To control the microscope and for data acquisition, custom-written software was used (LabView, National Instruments Corporation, Austin, TX, USA).
As a pre-test to check for vital preparation and successful staining procedure, we induced neuronal activity by stimulating the right antenna with two air puffs containing an odor mixture of citral and octanol (Aldrich Chemical Company, Inc.). The odors were loaded on a strip of filter paper (10μl of each odor at a concentration of 10−2, with hexane as solvent; Aldrich Chemical Company, Inc.). After evaporation of the solvent for 4min, the filter paper was placed into a syringe that was connected to a silicon tube used for stimulus application. The odor stimuli were applied manually 5 and 15s after the recording was triggered.
Only those animals in which odor-elicited neuronal activity could be measured were subsequently used in the experiments designed to investigate the representation of thermal information within the antennal lobe. To generate warm (30°C) or cold (15°C) air stimuli, an airflow was channeled through a custom-made heat exchanger connected to a water bath via two silicon tubes (DC1, Haake, Germany, see Ruchty et al., 2010 for details). During both, odor and temperature stimulation a constant airflow (ca. 1.5l/min) with stable room temperature of 24°C was blown over the preparation. The outlet of the stimulus air tube was positioned close to the ant's right antenna (2cm distance) opposite to the continuous airflow. Temperature in both airflows was continuously measured by a thermocouple (ALMEMO, Ahlborn Messtechnik, Holzkirchen, Germany).
Functional data were collected by acquiring images with 128×128pixel resolution and at a frame rate of 4 Hz. To screen the entire antennal lobe with all glomeruli for responses to temperature changes, we conducted 10–15 consecutive framescans (trials) in 10μm steps along the z-axis. In order to prevent neuronal adaptation in the thermosensitive neurons, we spaced the trials with a time interval of 2min. During each trial the antenna was stimulated four times, every 20 frames (5s) for a period of 2s, by switching the stimulus airflow onto the antenna using a solenoid valve (Lee, USA) that was controlled by the data capture software. Having acquired the functional data, we recorded image stacks of the whole antennal lobe volume with a higher optical resolution (256×256, 2μm step size).
For data processing, the raw fluorescence images (frame scans) were read into NIH ImageJ. To calculate the relative change in fluorescence (ΔF/F) we first subtracted the background fluorescence. The mean of the first 20 images was used as reference (F0) that was subtracted from each image in the sequence in order to obtain ΔF. The result (ΔF) was then divided by F0, which results in an image showing the relative fluorescence change (ΔF/F). An increase in cytosolic Ca2+, and thereby an increase in neuronal activity, causes a reduction in ΔF/F of the Fura-2 dye at an excitation wavelength of 810nm (Grynkiewicz et al., 1985).
An average image of all frames of each trial (100 frames) was calculated and used to select regions of interest (ROI) that corresponded to single glomeruli. Every recognizable glomerulus at each scan-depth was labeled with an individual ROI, and the relative fluorescence change (ΔF/F) over time (response kinetic) was analyzed. Apart from plotting the raw data traces, we visualized the changes in neuronal activity by calculating the average response during the four individual stimulus events. For this purpose the raw data image stack was sectioned into four substacks (each 25 frames long, e.g., frame 15–40 and frame 35–60) which were subsequently added and divided by 4. The relative change in fluorescence (ΔF/F) was calculated similar to the raw data; except that F0 was calculated as mean of the first five images of the four substacks (e.g., frame 15–20 or 35–40). In order to classify whether a glomerulus is thermosensitive or not, we first visually inspected the average traces looking for changes in ΔF/F. Glomeruli which showed precise responses to stimulus on- and offset were assigned thermosensitive as soon as ΔF/F exceeded the threshold value of 4%, which is well above spontaneous changes in fluorescence. The resulting changes in relative fluorescence (ΔF/F) could then be depicted as false color image sequence with blue and red indicating cold-sensitivity and warm-sensitivity of a glomerulus, respectively.
In order to map the position of thermosensitive glomeruli of different specimens in one common, averaged antennal lobe, we first moved the preparation in such a way that the anterior top of the antennal lobe in each specimen was centered. We then measured the x–y–z coordinates of every thermosensitive glomerulus in each of the investigated antennal lobes. In addition, we reconstructed an envelope of each antennal lobe, and by calculating the mean of all investigated antennal lobes (n=11), we obtained a normalized antennal lobe. The 3D positions of the thermosensitive glomeruli were mapped, based on their normalized coordinates, into the normalized antennal lobe.
Changes in relative fluorescence of all responding and some non-responding glomeruli and the spatial representation of temperature stimuli were illustrated using ORIGIN 8.1 (OriginLab, USA) and Adobe Illustrator (Adobe, San Jose, USA). The 3D-reconstruction of glomeruli was accomplished by using the software AMIRA 5 (Mercury Computer Systems, Berlin, Germany).
We selectively stained the receptor neurons of single sensilla coeloconica (Sc) in 19 independent preparations (antennae). In all of these cases, we found three receptor neuron axons, each innervating a single glomerulus in the same region within the ipsilateral antennal lobe (Example in Figures Figures1A,B).1A,B). All three innervated glomeruli are located in the dorsal part of the antennal lobe, at a distance of 80–110μm (depth) from its anterior surface and close to the dorsal lobe. Two of the innervated glomeruli are located at a lateral position, whereas the third glomerulus is located medially and is larger than the adjacent glomeruli in this region (Figure (Figure1B).1B). Because of their side-by-side position we termed the two lateral glomeruli Sc-L1 and Sc-L2 and later used them as landmarks. The medial glomerulus Sc-M, we could not use as a landmark because similar arrangements with a larger glomerulus are found in the dorsal part of the antennal lobe. This makes an unambiguous identification impossible.
All three neurons of a Sc have axons with a large diameter (mean=1.12μm, SD=0.089; n=6, measured at the unbranched axon after reconstruction, using the AMIRA measuring tool), branch within the glomeruli and densely innervate the whole glomerular lumen (Figures (Figures1B,C).1B,C). The diameters of these receptor neuron axons are significantly larger in comparison to the axons of olfactory hair sensilla (mean=0.62μm, SD=0.049, n=8, p<0.01; t-test). However, the shape and the size of the three glomeruli are similar to adjacent, putatively olfactory glomeruli (Figure (Figure1D).1D). Double-staining of receptor neuron axons from Sc (green) and from different types of hair sensilla (magenta) revealed that their glomerular innervation patterns do not overlap within the three Sc-glomeruli (double-staining: n=3, Figure Figure1D).1D). Thus, we conclude that the receptor neurons associated with Sc exclusively innervate the three Sc glomeruli.
In 257 out of 810 investigated animals, projection neurons from the two APTs could be stained successfully. Two-photon image stacks through the antennal lobes (ipsilateral to the injection site) revealed that in the successful attempts the overall majority of glomeruli was stained with calcium sensitive dye and thus amenable for functional imaging (Figure (Figure2A).2A). The spatial resolution of the obtained image stacks is exceptional in all three spatial dimensions and enables the reconstruction of single glomeruli or of the whole antennal lobe in 3D, on the basis of in vivo morphological data (Figures (Figures2A,B).2A,B). Landmarks like the macroglomerulus (Kleineidam et al., 2005; Kuebler et al., 2010) or the antennal nerve and its tracts within the antennal lobes can be used to locate the area where the receptor neurons of the Sc terminate. Based on their position within the antennal lobe and their characteristic shape and arrangement, the two Sc-L glomeruli can be identified and serve as landmark glomeruli to localize the potential location of the Sc-M glomerulus. The example in Figure Figure2B2B depicts the positions of the three glomeruli that are putatively innervated by receptor neuron axons of the Sc (solid spheres).
In a total of 20 specimens we recorded odor evoked neuronal activity, as indicated by a sudden drop in fluorescence (ΔF/F), which could be assigned to individual glomeruli of the antennal lobe. As an example, in Figure Figure2C2C an average image (100 recording frames) of an optical section through the antennal lobe is shown (depth=45μm). Upon stimulation with the odor mixture (10−2 citral and 10−2 octanol), one glomerulus responds strongly with an increase in neuronal activity.
The resulting increase in cytosolic Ca2+ concentration in the projection neurons leads to a rapid (within one frame) drop in fluorescence (ΔF/F≈11%; purple ROI and purple trace; Figure Figure2D).2D). The other glomeruli in the same optical section do not respond to this odor mixture.
Using two-photon microscopy we screened the whole antennal lobe and investigated where thermal information is represented. In 11 specimens we successfully recorded changes in neuronal activity within antennal lobe glomeruli in response to temperature stimuli. By using repeated stimulation with temperature steps, both, warm- and cold-sensitive glomeruli, could be identified. In the example of Figures Figures3A,B3A,B the fluorescent changes in response to repeated cold stimulation (15°C, n=4) are visualized as raw data traces (depth=49μm). Two glomeruli respond to cold stimulation (step change to 15°C; ambient temperature=24°C) with different response properties. The medial glomerulus (blue/white ROI and blue trace in Figures Figures3A,B)3A,B) responds with a drop in fluorescence upon stimulation (cold-sensitive glomerulus). In contrast, a central glomerulus (red ROI and red trace in Figures Figures3A,B)3A,B) seemed to be inhibited during the cold-stimuli and responded with increased activity after termination of the cold-stimuli (warm-sensitive glomerulus). There is a stronger Ca2+ signal in response to the temperature change in the cold-sensitive glomerulus (ΔF/F≈20%) than in the warm-sensitive glomerulus (ΔF/F≈10%). In Figure Figure3C3C the average response to four warm stimuli (30°C) is shown as false color image sequence (depth=100μm). Cold-sensitive glomeruli appear in blue, whereas red indicates warm-sensitive glomeruli (Figure (Figure3C).3C). Based on our criteria used to analyze the data, three warm-sensitive glomeruli and six cold-sensitive glomeruli can be detected within this example. The response kinetics of the individual glomeruli vary to some extent. For example, they exhibit different response latencies to the stimulus application (Figure (Figure3D).3D). The changes in relative fluorescence seem sometimes to be rapid, step-like (e.g., ROI 33, 34 or ROI 39), and sometimes the maximum change is reached considerably more slowly, e.g., in ROI 14.
Across all 11 investigated specimens, we detected between 1 and 10 thermosensitive glomeruli per antennal lobe (median: 4 glomeruli). Among the 47 thermosensitive glomeruli we investigated in total, the majority (n=40) respond with an increase in neuronal activity to cold-stimuli (15°C) whereas only 7 glomeruli respond with an increase in neuronal activity to warm stimuli (30°C). The majority of the thermosensitive glomeruli is located in the medially oriented half of the antennal lobe. Only 11 of the thermosensitive glomeruli are located at the upper 50μm from the anterior surface of the antennal lobe, whereas most of them are located at a depth between 70 and 120μm (n=29) (ventral view, Figure Figure4A).4A). Among the 47 thermosensitive glomeruli, 8 glomeruli are clustered medially (100–120μm from the lateral margin, ventral view, Figure Figure4A)4A) at a depth of 80–110μm along the anterior/posterior axis. This position corresponds to where we also found the Sc-M glomerulus during the single-staining of Sc (ventral view, Figure Figure4A,4A, medial black sphere). Most often (33 times) we detected thermosensitive glomeruli in the dorsal part of the antennal lobe at a distance of approximately 20–80μm from the dorsal margin (anterior view,Figure 4B).
In a number of specimens (n=8) we could identify the Sc-L glomeruli by focusing through the lower (posterior) part of the antennal lobe. We specifically investigated their potential temperature sensitivity in two examples. Our investigations revealed that the Sc-L glomeruli were insensitive to temperature stimuli irrespective of whether warm (30°C) or cold (15°C) temperature changes are presented (Figures (Figures5A–F).5A–F). In Figure Figure5A5A the two Sc-L glomeruli can clearly be distinguished. They do not respond to stimulation with cold-stimuli (15°C, green and gray ROIs, depth=95μm; raw data shown in Figure Figure5B,5B, average signal in Figure Figure5C).5C). In the medial part, where the third target glomerulus of the Sc is located (Sc-M glomerulus), we identified two glomeruli as candidates based on their relative position to the Sc-L glomeruli (black and blue ROIs, Figures Figures5B,C).5B,C). The dorsal glomerulus (black ROI) is stained only weakly. It does not exhibit any substantial activity changes upon temperature stimulation (15°C). However, the second candidate glomerulus (30μm ventrally, blue ROI) responds with strong oscillations in fluorescence to the applied stimuli (cold-sensitive glomerulus; blue ROI, ΔF/F≈10%).
The second example also shows that the Sc-L glomeruli are not responding to the temperature stimuli (Figures (Figures5D–F,5D–F, 30°C, gray and green ROIs). Considering the raw data traces shown in Figure Figure5E5E both medial candidate glomeruli respond to the stimulation with warm air in this example (blue ROI, ΔF/F≈6%, black ROI, ΔF/F≈10%). Based on its response characteristics, the ventral glomerulus (blue ROI, Figure Figure5D)5D) classifies as cold-sensitive glomerulus. The dorsal candidate glomerulus (black ROI, Figure Figure5D)5D) responds to the temperature stimuli slightly differently. During the first stimulus the glomerulus seems to respond as a warm-sensitive glomerulus. However, the response characteristic to the consecutive stimulations classifies this glomerulus as a cold-sensitive one. This is verified by the average signal of the four stimulus trials which shows that the dorsal glomerulus is indeed cold-sensitive (Figure (Figure5F,5F, black trace).
Throughout all recordings we never found thermosensitive glomeruli in the area of the antennal lobe where the two Sc-L glomeruli are located (Figures (Figures4A,B,4A,B, black spheres). The correlation of the functional imaging data with the innervation pattern of the Sc provides evidence that the temperature information received by these particular sensilla is sent to the Sc-M glomerulus in the antennal lobe.
In the present study, we show that the receptor neurons of thermosensitive sensilla coeloconica (Sc) project to the first olfactory neuropil, the antennal lobe. Within the antennal lobe, each of the three receptor neuron axons innervates a single glomerulus. Two of the three glomeruli are located side-by-side at a lateral position in the antennal lobe (Sc-L glomeruli), while the third one is located medially. Using two-photon Ca2+ imaging of antennal lobe projection neurons, we identified up to 10 thermosensitive glomeruli within a single antennal lobe. We found both warm and cold-sensitive glomeruli, which were mainly located in the medial half of the antennal lobe. The two lateral Sc-L glomeruli targeted by receptor neurons of the Sc are insensitive to temperature stimuli, and we never detected thermosensitive glomeruli in that specific area of the antennal lobe. In contrast, we found medial thermosensitive glomeruli at the position where the medial target glomerulus (Sc-M glomerulus) was located. Based on these lines of evidence, we conclude that thermal information received by the thermosensitive neuron of the Sc is processed in the Sc-M glomerulus.
The selective staining of single Sc resulted in three labeled axons, which all projected to the antennal lobe. This number corresponds to the number of receptor neurons identified in a previous study on the fine-structure of the Sc (Ruchty et al., 2009). All three labeled axons densely innervated a single glomerulus each. The three target glomeruli were located in the dorsal part of the ipsilateral antennal lobe at a distance between 80 and 110μm from its anterior surface (the entire antennal lobe spans approximately 150μm from anterior to posterior). In the cockroach, the axons of two types of thermosensitive sensilla innervate glomeruli at a similar (dorsal/posterior) region of the antennal lobe, and the thermosensitive neurons (one per sensillum) of both sensilla converge in a single glomerulus (Nishikawa et al., 1995). Electrophysiological recordings in the same species revealed thermosensitive projection- and interneurons in the medial/posterior part of the antennal lobe (Waldow, 1975; Nishikawa et al., 1995; Zeiner and Tichy, 2000; Fischer and Tichy, 2002; Nishino et al., 2003). Studies on the central projections from Sc on the antennae of honeybees (Nishino et al., 2009) and carpenter ants (Nakanishi et al., 2010) suggest similar target regions, although due to the experimental approach used in these two studies, other target region, e.g., the dorsal lobe, cannot be excluded.
Based on the similar position of the target glomeruli of thermosensitive neurons in the leaf-cutting ant and the cockroach, as well as the putative region in the honeybee and the carpenter ant, we assume that in insects in general antennal thermosensitive neurons terminate in specific glomeruli located in similar regions within the antennal lobe. These findings suggest a conserved representation of thermal information in the antennal lobe across insect taxa.
Compared to olfactory sensilla, thermosensitive sensilla occur in low numbers on the antenna of insects (Dumpert, 1972; Tominaga and Yokohari, 1982; Itoh et al., 1984; Hashimoto, 1990; Renthal et al., 2003). In the leaf-cutting ant Atta vollenweideri only about 12 Sc have been discovered on each antenna (Ruchty et al., 2009). In olfactory glomeruli it has repeatedly been shown that the size of a glomerulus is related to the number of receptor neuron axons terminating in the glomerulus (Hansson et al., 1995; Berg et al., 1998; Kleineidam et al., 2005; Kelber et al., 2010). The present study shows that the three Sc-glomeruli have a similar volume compared to the adjacent glomeruli, which are targeted by receptor neuron axons from olfactory sensilla (Kelber et al., 2010). Based on the relation between glomerular volume and number of innervating receptor neuron axons, a considerably smaller volume of the Sc-glomeruli would have been expected. To explain our contrasting finding, we hypothesize that the Sc-neurons occupy a larger volume of their glomeruli because of the larger axon diameters we found, compared to olfactory receptor neurons. This seems to be a common property of receptor neurons associated with Sc in Hymenoptera, since similar results have recently also been shown in honeybees and carpenter ants (Nishino et al., 2009; Nakanishi et al., 2010). Large axon diameters result in fast information propagation and thus may facilitate rapid behavioral responses to, e.g., temperaturechanges.
Two-photon Ca2+ imaging has so far been applied in insects for physiological studies of the olfactory system in the fruit fly (Drosophila; Wang et al., 2003; Suh et al., 2004; Jayaraman and Laurent, 2007; Root et al., 2007; Sachse et al., 2007) and the migratory locust (Locusta; Moreaux and Laurent, 2007) as well as of the visual system in the blowfly (Calliphora; Haag et al., 2004; Kalb et al., 2004; Kurtz et al., 2006; Spalthoff et al., 2010). In the present study, we use the two-photon microscope for the first time to acquire functional and morphological data of the antennal lobe in a social insect. Compared to conventional imaging, the major advantages of this imaging technique are the reduced dye bleaching and tissue damage and the enhanced imaging depth (Helmchen and Denk, 2005). These properties allow physiological access to the whole antennal lobe in this ant species. Due to the high z-resolution, the 3D reconstruction of single glomeruli and the whole neuropil is possible in parallel to the physiological investigation based on in vivo data. This is a major advantage compared to conventional methods like confocal laser scanning microscopy in which the brains have to be dissected and treated with dehydrating chemicals and clearing solutions, in order to obtain morphological data of insect brains or brain neuropils. Especially the dehydration of neuronal tissue leads to shrinking artifacts, which bias volume-based data acquisition (Bucher et al., 2000).
We screened the whole antennal lobe volume in search for thermosensitive glomeruli by performing 10–15 consecutive framescans each shifted by 10μm in z-axis. Although we did not quantify the number of glomeruli that were accessible, we are confident that we investigated the great majority of all glomeruli. However, because of the step size chosen (10μm) it cannot be excluded that we may have missed to record from a small percentage of thermosensitive glomeruli during data acquisition. The mean diameter of the glomeruli in the antennal lobe of Atta vollenweideri is about 6.30μm (Kelber et al., 2010), but an adequate step size to securely capture all glomeruli would have resulted in an experimental protocol exceeding the life time of the preparation. In addition to this experimental limitation, the variances in dye loading of projection neurons possibly resulted in an oversight of thermosensitive glomeruli. Our dye application resulted in some projection neurons loaded heavily with calcium indicator, while others were stained only weakly. Exceedingly high dye concentrations in projection neurons lead to considerable buffering of Ca2+, and weak staining may result in only marginal fluorescence changes. In both cases the applied temperature stimulus may well have elicited neuronal activity changes without causing a measurable change in fluorescence (example Figure Figure5B,5B, black ROI).
The number of thermosensitive glomeruli in the antennal lobe of the leaf-cutting ant possibly reflects the number of different types of thermosensitive neurons in different sensilla on the antenna. Thermosensitive neurons, which differ in their physiological response characteristics are necessary to assess different parameters of the thermal environment, which is a prerequisite for a variety of temperature-guided behaviors. It has recently been shown that the thermosensitive neuron housed in a Sc is extremely sensitive (temperature transients of ΔT=0.005°C can be distinguished), and that the neuron is physiologically adapted to detect rapid and minute temperature changes (Ruchty et al., 2009, 2010). Via sensory adaptation the sensitivity of the neuron is maintained over a wide range of ambient temperatures. Functionally, a role of this sensillum in the thermal landmark learning has been suggested in leaf-cutting ants (Kleineidam et al., 2007; Ruchty et al., 2009, 2010).
Based on the stimulation protocol used in the present study, we were not able to investigate the physiological characteristics of the projection neurons completely, e.g., in terms of adaptation abilities and response characteristics. But our results already show quite considerable differences in response characteristics between different glomeruli in terms of response latency and response dynamics. This indicates that several thermosensitive neurons with varying physiological characteristics send their axons to antennal lobe glomeruli. It would be of great interest whether the receptor neuron physiology, e.g., of the Sc, predicts the physiology of the projection neuron on which they synapse.
Neurons that do not adapt as strongly as the thermosensitive neurons of Sc, thereby providing the animals with information about the actual ambient temperature in their surrounding, have been described in antennal sensilla of the migratory locust Locusta migratoria (Waldow, 1970; Ameismeier and Loftus, 1988), the cockroach Periplaneta americana (Nishikawa et al., 1992) and the honeybee Apis mellifera (Lacher, 1964). In ants, neurons with such non-adapting physiological characteristics are expected as well, since ants can assess and respond to steady temperatures with very high accuracy, e.g., during brood care (Roces and Núñez, 1989, 1995; Weidenmüller et al., 2009). Possible candidate sensilla to house thermosensitive neurons with that particular physiological characteristics are the sensilla coelocapitula (Yokohari, 1983). We assume that these putative antennal thermosensitive sensilla send their axons to the antennal lobe as well.
In 11 different individuals we found a total of 47 thermosensitive glomeruli with a maximum of 10 in a single antennal lobe. Although most of the discovered glomeruli were cold-sensitive glomeruli, which responded with increasing neuronal activity to negative temperature steps, we also found a couple of warm-sensitive glomeruli (n=7). Due to the fact that each neuron is, at least to some extent, sensitive to temperature stimuli and increases its neuronal activity with increasing temperature, we cannot exclude unspecific temperature responses for the warm-sensitive glomeruli discovered here.
Apart from unspecific thermosensitivity there are several other possibilities which could potentially result in warm-sensitive glomeruli. The most obvious explanation is that warm-sensitive receptor neurons occur in addition to the already discovered cold-sensitive ones on the antennae. Warm-sensitive antennal neurons were discovered, but not further investigated, in a closely related leaf-cutting ant species (Kleineidam and Tautz, 1996). Furthermore, the presence of warm-sensitive projection neurons as discovered in the present study does not necessarily require warm-sensitive receptor neurons in the periphery. In the cockroach, warm-sensitive projection neurons and interneurons were found, although no antennal warm-sensitive neurons have been discovered there so far (Nishikawa et al., 1995; Zeiner and Tichy, 2000; Fischer and Tichy, 2002). Fischer and Tichy (2002) speculated that the response of warm-sensitive projection neurons was the result of the antennal lobe network, where the input from cold-sensitive receptor neurons to their target glomeruli may lead to a disinhibition of other glomeruli and hence to inverted response characteristics (Fischer and Tichy, 2002).
A further plausible explanation could be that the respective projection neurons are not at all driven by antennal neurons but rather excited via central thermosensitive neurons comparable to the recently discovered warm-sensitive anterior cell neurons involved in thermoregulation in Drosophila (Hamada et al., 2008). Whether the recorded increase of neuronal activity in projection neurons to warm stimuli is the result of neuronal activity in a peripheral or a central thermosensitive neuron or whether the neuronal network within the antennal lobe triggers the response has to be shown in future experiments.
The comparison of the receptor neuron staining and the Ca2+ imaging experiments led us to conclude that the thermosensitive neuron of the Sc innervates the Sc-M glomerulus. Three lines of evidence allow this conclusion. (1) The screening of the antennal lobe for thermosensitive glomeruli clearly showed that the area where the two Sc-L glomeruli are located is spared by thermosensitive glomeruli, and (2) that thermal information is mainly processed within the medial part of the neuropil where we found in six specimens a single cold-sensitive glomerulus, closely located to the position of the Sc-M glomerulus (Figures (Figures4A,B).4A,B). (3) Our conclusion is further supported by the functional imaging data of the two Sc-L glomeruli, which did not exhibit any sensitivity to thermal stimuli (Figures (Figures5A–F).5A–F). Unfortunately, we could not identify the medial Sc-glomerulus unambiguously during the experiments. Using the Sc-L glomeruli as landmarks, we identified two cold-sensitive candidate glomeruli of which one is supposed to be the target of the Sc thermosensitive neuron (Sc-M glomerulus) (Figures (Figures5A–F).5A–F). Future experiments, which for instance combine the anterograde labeling of the receptor neurons of a single Sc (leaving the other sensilla intact), together with functional imaging of the projection neurons may reveal which one of the two medial candidates is indeed the thermosensitive Sc-M glomerulus.
The state-of-the-art imaging technique used in the present study enabled us to investigate the general representation of thermal information within the antennal lobe. The role of the first olfactory neuropil in thermosensation can now be studied in greater detail to unravel the underlying neuronal mechanisms of specific temperature-guided behaviors in ants and other insects.
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.
We thank F. Roces for providing the leaf-cutting ants, C. Kelber for her assistance during the 3D reconstructions presented in the present manuscript and M. Nagel for assisting during the double-staining approach. We are grateful to H. Kasper for his technical assistance during two-photon microscopy. We thank Olympus for the loan of the 25× objective used during the two-photon microscopy study.
DFG: SFB 554 A6 and E1; SPP 1392 KL1327/2. Rüdiger Wehner was a Humboldt Awardee at the Biocenter of the University of Würzburg