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First published online May 1, 2006
Journal of Experimental Biology 209, 1914-1927 (2006)
Published by The Company of Biologists 2006
doi: 10.1242/jeb.02206

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Vomeronasal sensory neurons from Sternotherus odoratus (stinkpot/musk turtle) respond to chemosignals via the phospholipase C system

Jessica H. Brann^1,* and Debra A. Fadool^1,2,

¹ The Florida State University, Department of Biological Science, Program in Neuroscience, Biomedical Research Facility, Tallahassee, FL 32306, USA
² The Florida State University, Department of Biological Science, Program in Molecular Biophysics, Biomedical Research Facility, Tallahassee, FL 32306, USA

Author for correspondence (e-mail: dfadool{at}bio.fsu.edu)

Accepted 13 March 2006

	Summary

TOP Summary Introduction Materials and methods Results Discussion List of abbreviations References

 
The mammalian signal transduction apparatus utilized by vomeronasal sensory neurons (VSNs) in the vomeronasal organ (VNO) has been richly explored, while that of reptiles, and in particular, the stinkpot or musk turtle Sternotherus odoratus, is less understood. Given that the turtle's well-known reproductive and mating behaviors are governed by chemical communication, 247 patch-clamp recordings were made from male and female S. odoratus VSNs to study the chemosignal-activated properties as well as the second-messenger system underlying the receptor potential. Of the total neurons tested, 88 (35%) were responsive to at least one of five complex natural chemicals, some of which demonstrated a degree of sexual dimorphism in response selectivity. Most notably, male VSNs responded to male urine with solely outward currents. Ruthenium Red, an IP₃ receptor (IP₃R) antagonist, failed to block chemosignal-activated currents, while the phospholipase C (PLC) inhibitor, U73122, abolished the chemosignal-activated current within 2 min, implicating the PLC system in the generation of a receptor potential in the VNO of musk turtles. Dialysis of several second messengers or their analogues failed to elicit currents in the whole-cell patch-clamp configuration, negating a direct gating of the transduction channel by cyclic adenosine monophosphate (cAMP), inositol 1,4,5-trisphosphate (IP₃), arachidonic acid (AA), or diacylglycerol (DAG). Reversal potential analysis of chemosignal-evoked currents demonstrated that inward currents reversed at –5.7±7.8 mV (mean ± s.e.m.; N=10), while outward currents reversed at –28.2±2.4 mV (N=30). Measurements of conductance changes associated with outward currents indicated that the outward current represents a reduction of a steady state inward current by the closure of an ion channel when the VSN is exposed to a chemical stimulus such as male urine. Chemosignal-activated currents were significantly reduced when a peptide mimicking a domain on canonical transient receptor potential 2 (TRPC2), to which type 3 IP₃ receptor (IP₃R3) binds, was included in the recording pipette. Collectively these data suggest that there are multiple transduction cascades operational in the VSNs of S. odoratus, one of which may be mediated by a non-selective cation conductance that is not gated by IP₃ but may be modulated by the interaction of its receptor with the TRPC2 channel.

Key words: olfaction, VNO, transduction, PLC, TRPC2, inositol 1,4,5-trisphosphate receptor (IP₃R), musk turtle, Sternotherus odoratus

	Introduction

TOP Summary Introduction Materials and methods Results Discussion List of abbreviations References

 
The accessory olfactory system (AOS) has been well established as a primary detector for odor information concerning social organization and reproductive status (Halpern and Martínez-Marcos, 2003). In addition, in reptilian species such as the turtle, lizard and garter snake, the AOS also serves to detect prey items (Wang et al., 1997; Fadool et al., 2001; Vitt et al., 2003). The best-studied peripheral sensory organ for the AOS is the vomeronasal organ (VNO). Sexual dimorphism in the reptilian and amphibian VNO is found at both the level of gross anatomy (Dawley, 1998) and the single sensory neuron (Fadool et al., 2001). There are sexually distinct differences in vomeronasal sensory neuron (VSN) soma diameter as well as in the composition and kinetics of voltage-activated conductances (Fadool et al., 2001).

In terrestrial vertebrates, the VNO is a compartment of the olfactory system that is separate and distinct from the main olfactory system (MOS). In reptiles, it is larger than the main olfactory epithelium (MOE), the sensory organ for the MOS (Ernst et al., 1994; Murphy et al., 2001; Labra et al., 2005). In most animal classes, the VNO is thought to mediate primarily pheromonal signals, but not exclusively (Baxi et al., 2006). Pheromones [originally described by Karlson and Lüscher (Karlson and Lüscher, 1959)] are substances that are secreted to the external environment by an individual and received by a second individual of the same species, in which they release a specific reaction, for example, a definite behavior or a developmental process (Rodriguez et al., 2002). While the VNO is responsive to pheromones, it also detects a variety of chemosignals that may not fit within the classical definition of a pheromone. Often, the VNO is considered a detector of nonvolatile odorants, but this assertion is incorrect, since the VNO detects volatile odorants as well (O'Connell and Meredith, 1984; Meredith, 1991; Meredith, 2001; Halpern and Martínez-Marcos, 2003; Trinh and Storm, 2003; Leinders-Zufall et al., 2004). In addition, the MOE is known to respond to some pheromones (Restrepo et al., 2004). Hence we will use the term `chemosignal' to incorporate any chemical received by the VNO and potentially able to elicit an electrical signal encoded by this organ for chemical communication.

Although a limited amount of published molecular chemoreceptor information is available for reptiles (i.e. Vogt et al., 2002), it is generally believed that the initial VNO transduction event is governed by the binding of chemosignals to G-protein coupled receptors (GPCRs), as well described for rodents (Dulac and Axel, 1995; Herrada and Dulac, 1997; Matsunami and Buck, 1997; Ryba and Tirindelli, 1997; Pantages and Dulac, 2000). Although the nucleotide sequence and expression patterns of these receptors have not yet been published for the reptilian VNO, we do know that in the common musk/stinkpot turtle Sternotherus odoratus they must be coupled to the downstream G-protein G_i, which has restricted expression in the microvilli of the turtle VSNs, is expressed at greater levels in male versus female turtle VNO, and is developmentally increased in the VNO coincident with reproductive maturity of the turtles (Murphy et al., 2001). More is known for the downstream signaling cascade found in this species, in which there appears to be continuity with that known for rodents. Rodent VSNs utilize phospholipase C (PLC) signaling (Runnenburger et al., 2002) to cleave phosphatidyl-inositol bis-phosphate (PIP₂) into diacylglycerol (DAG) and inositol 1,4,5-trisphosphate (IP₃) second messengers (Berridge and Irvine, 1984). DAG or one of its derivatives, arachidonic acid (AA), may activate the ion channel responsible for carrying the chemosignal-activated current, the canonical transient receptor potential channel, TRPC2 (Spehr et al., 2002; Lucas et al., 2003). This channel is a six-transmembrane domain nonselective cation channel and is a member of the TRP ion channel superfamily (Minke and Cook, 2002). TRPC2 is expressed in the microvilli of rats, mice and turtles (Liman et al., 1999; Murphy et al., 2001; Leypold et al., 2002; Stowers et al., 2002). In both rodents and turtles, TRPC2 shows a developmental pattern of expression, with an increased expression correlated to sexual maturity (Murphy et al., 2001). TRPC2 and the type III inositol 1,4,5-trisphospate receptor (IP₃R3) demonstrate co-localization in VSN microvilli and can be coimmunoprecipitated from rodent VNO (Brann et al., 2002), but the functional relevance of this protein–protein interaction is yet unknown.

Several questions remain unanswered, therefore, when discussing transduction in the VNO of S. odoratus and downstream vertebrate VNO transduction in general. First, it is not clear whether PLC signaling is important to the generation of a receptor potential in the turtle VNO. Second, it is unknown if, and how, TRPC2 is activated in the turtle. Third, TRPC2 in mouse VSNs was shown to be activated by an analogue of diacylglycerol (DAG), independently of IP₃ (Lucas et al., 2003), therefore it is unknown if a TRPC2/IP₃R3 complex is required for the final transduction event, or simply provides a form of modulation of the transduction current. Fourth, DAG (and its derivatives) has now been shown to activate TRPC3 and TRPC6 (Chyb et al., 1999; Hofmann et al., 1999; Clapham et al., 2001; Venkatachalam et al., 2001; Albert and Large, 2003; Pocock et al., 2004), and may also have a role in the VNO (Spehr et al., 2002; Lucas et al., 2003). The dialysis of a natural DAG analogue (called SAG) into rodent VSNs, however, did not elicit a current with chemosignal-like kinetics. Nonetheless, the effectiveness of SAG as an activator of the cation channel was severely diminished in TRPC2-null mice, suggesting that TRPC2 is the channel activated by SAG (Lucas et al., 2003). DAG has been reported to not activate TRPC1, TRPC4 or TRPC5 (Hofmann et al., 1999; Venkatachalam et al., 2003). Together, these studies demonstrate a putative direct role of DAG in gating TRPC2, but do not address possible modulation, amplification or regulation of the primary cationic conductance by IP₃Rs mediated by the protein–protein interaction between TRPC2 and IP₃R3.

Here, we explore currents elicited with several natural chemosignals, including urine, a reproductive musk and a prey item. The use of the PLC system in the transduction of chemosignal information is examined pharmacologically, and reversal potential analysis is used to demonstrate the presence of two separate ionic conductances found in the musk turtle VNO. Finally, the role of the signaling complex between TRPC2 and IP₃R3 in the turtle is examined by disruption of the complex with a peptide inhibitor.

	Materials and methods

TOP Summary Introduction Materials and methods Results Discussion List of abbreviations References

 
Animal collection, care, and maintenance
Sternotherus odoratus Latreille (stinkpot or common musk turtle) were hand-caught during the reproductive season (April to September) at Indian Pines (Opelika, AL, USA) or Lake Jackson (Tallahassee, FL, USA) with permission from the State of Alabama Department of Conservation and the State of Florida Fish and Wildlife Conservation Commission. Turtles were housed for short periods, usually 1–2 months, in 10 gallon (38 l) aquaria with rocks for basking, maintained on a 15 h:9 h light:dark cycle and fed a standard diet of catfish pellets (Florida Farm and Feed, Tallahassee, FL, USA). Turtles used in the described experiments were adults (Ernst et al., 1994; Fadool et al., 2001). Mass and plastron length were noted on the day of capture as well as on the day of experimental use. The plastron, or ventral shell, of a turtle is often used to measure growth or size of the animal, given the more variable curvature of the dorsal carapace (Ernst et al., 1994). All procedures were performed in accordance with The Florida State University Animal Care and Use Committee.

Solutions
Ca²⁺-free Ringer contained (in mmol l^–1): 116 NaCl, 4 KCl, 1 MgCl₂, 15 glucose, 10 Hepes, 10 EGTA, pH 7.4. Ringer contained (in mmol l^–1): 116 NaCl, 4 KCl, 1 CaCl₂, 1 MgCl₂, 15 glucose, 10 Hepes, 5 sodium pyruvate, pH 7.4. Pipette solution contained (in mmol l^–1): 100 KCl, 20 NaCl, 10 Hepes, 2 MgCl₂, 1.1 EGTA, 0.8 CaCl₂, 2.5 ATP, 0.5 GTP, pH 7.4. Phosphate-buffered saline (PBS) contained (in mmol l^–1): 137 NaCl, 2.7 KCl, 10 Na₂HPO₄, 2 KH₂PO₄, pH 7.4. All chemicals were obtained from either Sigma Chemical Company (St Louis, MO, USA) or Fisher Scientific (Fairlawn, NJ, USA).

Electrophysiology
Turtles were killed by administering a lethal intraperitoneal dose of sodium pentabarbitol (Butler Company, Columbus, OH, USA), followed by decapitation. The VNO was quickly dissected, grossly cut into quarters, and incubated in L-cysteine-activated papain (Worthington Biochemical Corp., Lakewood, NJ, USA) in Ca²⁺-free Ringer for 15–18 min while gently rotated at 30 r.p.m. (Orbital Shaker, Model 3520, Lab-Line Instruments, Melrose Park, IL, USA) at room temperature (RT). Following enzymatic treatment, quarters could be held at 4°C for up to 8 h prior to physical dissociation. Sensory neurons were physically dissociated by trituration using a size-graded series of fire-polished siliconized Pasteur pipettes and were then plated on to 0.01% poly-D-lysine hydrobromide (Sigma) and 0.1% laminin (BD Biosciences, San Jose, CA, USA) coated Corning #25000 dishes (Fisher) (Leinders-Zufall et al., 1997).

Acutely isolated vomeronasal sensory neurons (VSNs) were viewed at 40x magnification (Axiovert 135, Carl Zeiss, Thornwood, NY, USA) with Hoffman modulation contrast optics for patch-clamp recording (Hamill et al., 1981). Patch pipettes were fabricated from Jencons borosilicate glass (catalog number M15/10; Jencons Limited, Bedfordshire, UK), fire-polished to approximately 1 µm (bubble number 5.0) (Mittman et al., 1987) and coated near the tip with beeswax to reduce the pipette capacitance. Pipette resistances were between 7 and 10 M, which produced high-resistance seals (between 8 and 14 G) by applying gentle suction to the lumen of the pipette upon contact with the cell. In all experiments, cells were voltage-clamped at a holding potential (V_h) of –60 mV, unless specified otherwise. Voltage- and chemically activated currents were recorded in the whole-cell configuration using an integrating patch-clamp amplifier (Axopatch 200B, Axon Instruments, Union City, CA, USA). The analog output was filtered at 5 kHz and digitally sampled every 0.5–4 ms. Data acquisition, storage and analysis of the digitized recordings were carried out using pClamp8.0 software (Axon Instruments) in conjunction with Origin 4.1 (Microcal Software, Inc., Northampton, MA, USA), SigmaPlot 8.0 and SigmaStat 3.0 (Systat Software, Point Richmond, CA, USA). Statistical tests are as noted, with statistical significance in all tests defined at the 95% confidence interval (Steel and Torrie, 1980).

Second messengers and pharmacological agents
Second messengers and non-permeant analogues were introduced via the pipette during whole-cell recording. To promote seal formation and initial controlled recording conditions, pipettes were tip-filled 1–2 mm with control patch solution and then back-filled with messenger or analogue; a method we have previously calibrated and applied (Fadool and Ache, 1992). Cyclic adenosine monophosphate (cAMP; 0.5 or 1 µmol l^–1; back-fill pipette; Sigma) and inositol 1,4,5-trisphosphate (IP₃; 1–100 µmol l^–1; back-fill pipette, Sigma) were made as a stock solution stored at –20°C and diluted in pipette solution daily. Arachidonic acid (AA; 10 µmol l^–1; back-fill pipette; Calbiochem, San Diego, CA, USA), a non-cell permeable polyunsaturated fatty acid (PUFA) derived from DAG by a DAG lipase or from phospholipids by phospholipase A₂ (Spehr et al., 2002), was prepared fresh daily in pipette solution. 1-Oleoyl-2-acetyl-sn-glycerol (OAG; 100 µmol l^–1; both bath application and back-fill pipette tested; Calbiochem) and 1-stearoyl-2-arachidonoyl-sn-glycerol (SAG; 100 µmol l^–1; back-fill pipette; Calbiochem), analogues of diacylglycerol (DAG), were reconstituted daily in DMSO (final concentration 0.1%). Ruthenium Red (RR), shown to inhibit IP₃-evoked currents (Fadool and Ache, 1992; Kashiwayanagi et al., 2000; Taniguchi et al., 2000), was freshly made daily in Ringer at a concentration of 1 mmol l^–1 and filtered (25 mm diameter, 0.2 µm pore size, Whatman, Clifton, NJ, USA) to avoid occlusion of the multi-barrel pipette (bath application; Sigma). U73122, an inhibitor of phospholipase C, was reconstituted in DMSO (final concentration 0.1%) and stored at –20°C as a stock solution (50 µmol l^–1; bath application; BioMol, Plymouth Meeting, PA, USA). A synthesized peptide (10 µmol l^–1) designed to target and interrupt the interaction domain between TRPC2 and IP₃R3 with the peptide sequence GSAGEGERVSYRLRVIK-ALVQRYIETARRE (905–934 mTRPC2) (Tang et al., 2001) was reconstituted in pipette solution and stored at –20°C until use (back-fill pipette; GeneMed Synthesis, Inc., South San Francisco, FL, USA). Based upon the mouse sequence for TRPC2 (GenBank accession no. AAD17196) (Vannier et al., 1999), we utilized web-based protein prediction software (called TMpred – Prediction of Transmembrane Regions and Orientation; http://www.ch.embnet.org/software/TMPRED_form.html,) to determine that the predicted binding would align with the intracellular C-terminal tail of the channel (Hofmann and Stoffel, 1993; Hirokawa et al., 1998).

Chemical stimulation
During the reproductive season (April–September), musk was harvested from Sternotherus odoratus once a month by gently milking the posterior reproductive musk gland. Musk samples obtained from a single animal ranged between 1–2 µl. Turtle urine was obtained post mortem by inserting a 27-gauge needle directly into the bladder. Catfish extract was prepared from a commercially available pellet (Florida Farm and Feed, Tallahassee, FL, USA). Pellets (2 g) were hydrated in 20 ml of high-quality water, ground by mortar and pestle, and then clarified by low-speed centrifugation for 5 min at room temperature. All samples were rapidly collected, placed on ice, and stored undiluted at –80°C until diluted in Ringer on the day of experimentation.

Chemosignals were spritzed (700 ms pulse) onto isolated VSNs using custom-fabricated seven-barrel glass micropipettes (1.2mm outer diameter, catalog no. 17-12-M; Frederick Haer, Bowdoinham, ME, USA) coupled to a pressurized valve system (Picospritzer, General Valve, Fairfield, NJ, USA). Dilution of the chemical between the multibarrelled pipette and the cell surface, an average distance of two cell diameters, was estimated to be approximately 9% on the basis of the calculated K⁺ permeability method (Firestein and Werblin, 1989). Chemical concentrations are reported as the pipette concentration and are not corrected for this dilution. The pipette concentration of urine was 1:5 from full strength, between 1:100 and 1:300 for musk, and between 1:100 and 1:1000 for catfish extract. All dilutions were prepared daily in turtle Ringer, which served as the control vehicle in all conditions. If a neuron responded to the control, it was assumed to be a mechanical stretch-activated response, and no further use was made of the cell. The peak magnitude of a response was measured as the difference in current from the baseline prior to presentation of the chemical to the peak outward- or inward-evoked current within 500 ms of valve activation of the picospritzer. Zero current (no response) was defined as no observable deflection or a deflection that was less than four times the total peak-to-peak (range) noise level (membrane plus equipment) under control baseline conditions.

	Results

TOP Summary Introduction Materials and methods Results Discussion List of abbreviations References

 
Mass and plastron length of Sternotherus odoratus
The mass of each turtle was recorded upon arrival in the laboratory, and again on the date of use for electrophysiological recording. As one metric of good animal husbandry, it was noted that a majority of animals grew both in plastron length and in mass over their time in captivity (data not shown; usually 1–2 months). A variety of turtles, including musk turtles, are well-known to be sexually dimorphic in size as traditionally indexed by the length of the plastron (Ernst et al., 1994). Over our 4-year collection, female musk turtles had longer plastrons than males, reaching statistical significance in years 2003 and 2004 [Fig. 1A, two-way ANOVA, Student–Neuman–Keuls (SNK) pairwise multiple comparison between sex and year, P0.05]. Using adult mass as a measure of dimorphism is not as reliable due to the fluctuation in the mass of the female during egg production (Fig. 1B).

View larger version (15K): [in this window] [in a new window]   Fig. 1. Plastron length and mass of Sternotherus odoratus, by year. (A) Adult female (filled circles) versus adult male (open squares) plastron length, S. odoratus versus collection year (asterisk denotes significantly different between sexes in years shown; mean ± s.e.m.; two-way ANOVA, SNK pairwise multiple comparison between sex and year, P0.05). (B) Mass of adult female (filled circles) and male (open squares) Sternotherus odoratus versus collection year (not significantly different; mean ± s.e.m.; two-way ANOVA, P0.05). N values are shown beside symbols.

Chemically activated properties
247 vomeronasal sensory neurons (VSNs) isolated from a total of 45 animals (31 females and 14 males) were tested for their ability to generate a current in response to stimulation with up to five different natural chemosignals (see Materials and methods; male musk, female musk, male urine, female urine and catfish extract). Each chemosignal was presented in the absence of the others, and the order of presentation was varied. Current responses of both inward and outward polarity typically rose to a maximum over several hundred milliseconds and subsequently declined to rest over a period of 3–4 s (Fig. 2). For all odor-exposure trials, neurons were clamped at a holding potential (V_h) of –60 mV, at which there is no voltage-gated channel activity. Eighty-eight of the 247 VSNs (35%) responded to the chemosignals presented (Fig. 3A). Of the 88 responsive VSNs, 40 (45%) responded to only one of the five chemicals presented in the array. The remaining VSNs (48 neurons, 55%) responded to between two and four of the five presented chemicals. None of the 88 VSNs responded to all five of the presented chemicals. The majority (64%) of VSNs responding to the tested chemosignals were isolated from female musk turtles due to animal collection bias, but females overall had a slightly lower response rate (defined by a response to at least one of the five chemicals presented; 34%) than did males (38%).

View larger version (10K): [in this window] [in a new window]   Fig. 2. Representative examples of chemosignal-activated current obtained with chemical stimulation of vomeronasal sensory neurons (VSNs). (A) A male vomeronasal sensory neuron (VSN) when stimulated with catfish extract exhibited an outward current, as defined by the polarity of the response obtained at holding potential Vh=–60 mV. The black bar above the trace denotes the time (700 ms) that the VSN was presented with chemosignal delivered via a pressurized glass pipette approximately two cell-widths away from the VSN. (B) As in A but for a female VSN stimulated with female musk. Current record is representative of an inward current, as defined by the polarity of the response obtained at Vh=–60 mV.

View larger version (31K): [in this window] [in a new window]   Fig. 3. The percentage of cells responding with a given polarity to a particular chemosignal is different between male and female vomeronasal sensory neurons (VSNs). (A) Histogram plot of the three different response categories of VSNs, separated on the basis of sex; male, gray; female, black. (B–F) Histogram plots of the percentage of female and male VSNs responding with an outward (black bars) or inward (white bars) current to (B) male musk, (C) female musk, (D) male urine, (E) female urine, (F) catfish extract. *Significantly different response frequency of inward and outward current across sex by 2 analysis, P0.05; NS, not significantly different. N values are shown beside bars.

The recorded mean input resistance (R_N) of 2.9±0.3 G (N=11) of VSNs at rest was similar to that previously recorded (Fadool et al., 2001) and also underscores the importance of small amplitude chemosignal-activated currents in these specialized sensory neurons. We have previously characterized the peak current response amplitudes for natural chemicals using an entropy (H metric) index from information theory that quantified the breadth of tuning for these neurons (Fadool et al., 2001). This study now furthers our initial characterization by exploring frequencies of response sorted to both sex and polarity. Here we report that chemosignal-activated currents can be of either polarity, depending on the cell and the chemosignal tested. Of the collective 165 responses generated by the 88 VSNs responding to chemosignals, outward currents were generated roughly twice as frequently as inward currents (107=outward responses; 58=inward responses; Fig. 3). The majority of chemosignals tested could evoke both inward and outward current dependent upon the individual VSN, but within a single VSN, a single chemosignal never elicited dual polarity, recording at a fixed command potential (V_c)=–60 mV. Most notably, a similar number of VSNs from females (17 cells, 30%) and males (6 cells, 20%) exhibited responses of both polarities when responsive to more than one chemosignal (data not shown). ² analysis of the frequency pattern of outward and inward chemosignal-evoked current responses between male and female neurons indicated that the response pattern to male musk, male urine and catfish extract is statistically different across sex (Fig. 3B,D,F). More female neurons responded to male musk than did male neurons, but the response to female musk was not significantly different across sex (Fig. 3B,C; ² analysis). Male urine evoked only outward currents in male VSNs (significantly different ² analysis; Fig. 3D) but the response to female urine was not significantly different across sex (Fig. 3E). The stimulus most frequently eliciting a current response in both male and female VSNs was catfish extract (males, 47%; females, 50%) and female urine (males, 47%; females 40%) (Fig. 3E,F).

Chemosignal responses were examined in the absence of pharmacological agents for possible attenuation with repeated stimulation over time. In Fig. 4A (top trace), an isolated VSN was patch-clamped in the whole-cell configuration at a V_h of –60 mV. The VSN was then exposed to a 700 ms puff of chemosignal, denoted by the black bar above the recording. The cell was then stimulated again at varying time intervals. The same chemosignal response 6 min after initial chemosignal exposure is shown in the bottom trace in Fig. 4A. As is shown in Fig. 4B, the normal chemosignal response was not altered over time (one-way repeated measures ANOVA, P0.05).

View larger version (24K): [in this window] [in a new window]   Fig. 4. Ruthenium Red (RR), an antagonist of the IP3R, fails to block chemosignal-activated currents in S. odoratus vomeronasal sensory neurons (VSNs) while an inhibitor of phospholipase C (U73122) does block chemosignal-activated currents. (A) A representative example of the response of a female VSN to catfish extract at 0 min (top trace) and 6 min later (bottom trace) without pharmacological perturbation. The chemosignal presentation is shown as black bar above the response. This particular cell was used primarily for reversal potential analysis, hence the VSN had been exposed to the chemical signal twelve times within the time span described. (B) Histogram plot of the normalized current magnitude (normalized to first exposure to chemosignal; t0) over time. Cells were sampled at varying time points (tn), such that not every cell was sampled for each of the time points. The amplitude of the chemosignal-activated current was not altered over 12 min (one-way repeated measures ANOVA, P0.05). (C) A representative example of the response of a female VSN to male urine at 0 min (top trace) and 6 min (bottom trace) following bath application of 1 mmol 1–1 RR. (D) Histogram plot of the normalized current magnitude (normalized to t0) over time. The chemosignal-activated current is not altered over 10 min (not significantly different by treatment or time, two-way repeated measures ANOVA, P0.05) in response to RR treatment. The normal chemosignal response over time is denoted by the broken line. (E) A representative example of the response of a female VSN to catfish extract at 0 min (top trace) and 8 min (bottom trace) following bath application of 50 µmol l–1 U73122. (F) As in D but for U73122 treatment. Asterisks denote significant difference between treatments, two-way repeated measures ANOVA, followed by SNK pairwise multiple comparison between treatment and time, P0.05). N values are shown beside bars. (A,C,E) Broken line denotes baseline current.

These experiments suggested that a plasma membrane IP₃R did not serve as the main carrier of the chemosignal-activated current in musk turtle VSNs, but two questions remained. First, it is not known whether the phospholipase C (PLC) system is required for the generation of chemosignal-activated currents in the musk turtle. Second, it is not clear what role, if any, the IP₃R may have in modulating the ion channel that is the primary carrier of the chemosignal-activated current. Therefore, a second set of VSNs were examined to investigate whether the chemosignal-activated current could be altered with the addition of a membrane-permeant phospholipase C inhibitor, U73122. Again, a baseline chemosignal response was obtained, 50 µmol 1^–1 U73122 was added to the bath, and chemosignal-activated current was monitored for the following 10 min (Fig. 4E). In this case, drug treatment with U73122 did rapidly (within 2 min) and significantly reduce the chemosignal-activated current, with the effect lasting for the duration of the test (Fig. 4F, significantly different, two-way repeated measures ANOVA, followed by SNK-pairwise multiple comparison between treatment and time, P0.05). The bath was not continually perfused, hence VSNs were not examined for washout recovery of the chemosignal-activated current. Neither the lack of response to RR (Fig. 4C,D) nor the reduction in current induced by U73122 (Fig. 4E,F) was dependent on current polarity, thus data were pooled for inward and outward current responses, and an example of each is demonstrated in the composition of this figure.

Second messenger analogues do not activate currents of either inward or outward polarity
Since the chemosignal-activated current was blocked by inhibiting phospholipase C, which would interfere with the generation of the two second messengers inositol 1,4,5-trisphosphate (IP₃) and diacylglycerol (DAG), we attempted to elicit currents that mimicked the chemosignal-activated current by including various second messenger analogues in the recording pipette while in the whole-cell configuration (Fig. 5). Fig. 5A is representative of recordings made at a V_h of –60 mV (below the threshold for voltage-activation). When 0.5 or 1 µmol 1^–1 cAMP, 240 µmol 1^–1 IP₃ or 125 µmol 1^–1 1-oleoyl-2-acetyl-sn-glycerol (OAG; an analogue of DAG) were included in the patch pipette, no deflections were seen (Fig. 5B–D). A polyunsaturated fatty acid (PUFA) derivative of DAG, arachidonic acid (AA), was also included in the recording pipette, but failed to induce current fluctuations other than rare rapid transients (Fig. 5E). An additional, naturally occurring DAG analogue, SAG, was also tested (Fig. 5F). SAG did not elicit a chemosignal-like response, but did appear to make the membrane unstable, probably due to its incorporation into the membrane. SAG was tested not only in the whole-cell configuration, but also on inside-out patches (N=4; data not shown), and in combination with IP₃ (N=5; data not shown), all of which failed to elicit chemosignal-like currents.

View larger version (26K): [in this window] [in a new window]   Fig. 5. Dialysis of the second messengers cAMP, IP3, OAG, arachidonic acid (AA), and SAG in isolated S. odoratus vomeronasal sensory neurons (VSNs). Analogues were made as described (see Materials and methods) and back-filled in the recording pipette to allow diffusion upon attaining the whole-cell configuration. VSNs were voltage-clamped at Vh=–60 mV. (A) A representative example of a VSN that had not been dialyzed with a second messenger analogue in order to illustrate stability of the patch. (B) 0.5 or 1 µmol l–1 cyclic adenosine monophosphate (cAMP) (N=27). (C) 240 µmol l–1 inositol 1,4,5-trisphosphate (IP3) (N=20). (D) 125 µmol l–1 1-oleoyl-2-acetyl-sn-glycerol (OAG), a membrane-permeant analogue of diacylglycerol (DAG), applied to either the bath surrounding the VSN or within the recording pipette (N=15). Trace shown is an example of pipette perfusion. (E) 10 µmol l–1 AA, a polyunsaturated fatty acid (PUFA) derivative of DAG (N=11). (F) 10 mmol l–1 1-stearoyl-2-arachidonoyl-sn-glycerol (SAG), a natural analogue of DAG (N=6).

View larger version (34K): [in this window] [in a new window]   Fig. 6. Analysis of chemosignal-activated reversal potentials supports a cationic receptor potential in vomeronasal sensory neurons (VSNs) of S. odoratus. (A,B) Response of a female neuron to (A) catfish extract (1:10 dilution), (B) female musk (1:100 dilution). Broken horizontal lines indicate baseline currents. (C,D) Plotted current–voltage relation for the families of currents evoked in A and B, respectively. (E,F) Scatter plot of estimated reversal potentials derived in C and D for chemosignal-evoked outward (E) and inward (F) currents, respectively. For each chemosignal, the vertical line depicts the mean reversal potential if more than one sample was obtained. The average reversal potential for the outward current was –28.2±2.37 mV (N=30) and that for the inward current was –5.7±7.79 mV (N=10).

In addition to probing the reversal potential for the chemosignal response, we were interested in whether chemosignal application was accompanied by conductance changes in the VSN. If the chemosignal caused an ion channel to open, membrane resistance would decrease and conductance would increase, according to Ohm's Law and the calculated time constant. However, if an odorant caused an ion channel to close, exactly the opposite would occur, and conductance would decrease. Conductance changes were measured by injecting a series of five hyperpolarizing pulses from V_h=–60 mV to –90 mV (V_c) before, during and after chemosignal stimulation eliciting outward currents (Fig. 7). Chemosignal-evoked inward currents were not tested. At rest, VSNs had a mean input resistance (R_N) of 2.9±0.3 G and a membrane time constant () of 17.7±3.2 ms (N=11). Analysis of the current at the peak of the chemosignal response, when compared to the same hyperpolarizing step before and after chemosignal exposure, revealed a significant reduction in current (from 10.9±0.8 to 6.6±0.9 pA) and conductance (from 6.3±1.3 to 1.0±0.3 pS). In addition, a concomitant significant increase in R_N (5.7±0.9 G) was seen as well as a significant decrease in to 4.3±1.2 ms (paired t-test, P0.05; Fig. 7).

View larger version (10K): [in this window] [in a new window]   Fig. 7. Vomeronasal sensory neurons (VSNs) from S. odoratus exhibit a chemosignal-evoked conductance decrease linked with outward currents. A VSN from a female S. odoratus was held at –60 mV (Vh) with five hyperpolarizing steps to –90 mV (Vc) injected prior (black), during (gray) and following (black) chemosignal stimulation with catfish extract. Inward chemosignal-evoked conductance changes were not tested.

A peptide directed against the TRPC2-IP₃R3 interaction domain blocks the chemosignal-activated current
We previously demonstrated that the ion channels TRPC2 and IP₃R3 participate in a protein–protein interaction in the VNO of the rat (Brann et al., 2002). The following experiments were designed to probe the question of a functional role of this protein–protein interaction, as well as to find possible common signal transduction mechanisms between the rat and the turtle. First, we sought to determine the functional role of the physical interaction between TRPC2 and IP₃R3. A recent publication using GST-fusion proteins of portions of these two channels demonstrated that calmodulin (CaM) and IP₃Rs share a common binding site on the carboxyl terminal of all TRPC channels (Tang et al., 2001). TRPC2 contains two such binding domains for CaM and all isoforms of the IP₃R, the first being amino acids 901–936, and the second being amino acids 942–1072. IP₃R3 also has a TRPC2 binding domain (amino acids 669–698) (Tang et al., 2001). We generated a peptide mimicking the first binding domain in the C terminus of TRPC2 (Fig. 8A), and included it in the patch pipette while recording from isolated VSNs in the whole-cell configuration and stimulating the VSN with a battery of different chemosignals (see Materials and methods). In all experiments, the designation 0 min is defined as the time at which the VSN was first exposed to a given chemosignal, or typically less than 30 s after breakthrough to the whole-cell configuration. A typical response from a VSN at 0 min is shown in the top trace of Fig. 8C. Inclusion of the peptide attenuated the chemosignal response within 5 min, with the effect lasting until 10 min (times later than 10 min were not tested) (Fig. 8B,C). Inclusion of boiled peptide in the recording pipette as a control did not alter the chemosignal response over 10 min (data not shown). Boiling results in denaturation of the peptide, and the peptide would presumably fail to bind the IP₃R, as has been demonstrated previously using similar peptide blocking approaches (Fadool and Ache, 1992; Holmes et al., 1996).

View larger version (21K): [in this window] [in a new window]   Fig. 8. A peptide directed against the interaction domain between TRPC2 and IP3R3 blocks the chemosignal-activated currents in S. odoratus vomeronasal sensory neurons (VSNs) when included in the patch pipette in the whole-cell configuration. (A) Amino acid sequence of the synthesized peptide (derived from mTRPC2, amino acids 905–934) (Tang et al., 2001). (B) Histogram plot of the chemosignal-activated current over 10 min when 10 µmol l–1 peptide is included in the recording pipette. The normal chemosignal-activated current over time is denoted by a broken line (see Fig. 4). Current obtained for each cell at varying time points (tn) was normalized to its first exposure to chemosignal (t0) Asterisks denote significant differences between control and peptide, two-way repeated measures ANOVA, followed by SNK pairwise multiple comparison between treatment and time, P0.05). (C) Representative example of peptide treatment. While in the whole-cell configuration, the VSN was presented with a chemosignal, and a baseline (immediately after the whole-cell configuration was obtained) recording was made (top). The same chemosignal-activated current is shown 10 min after peptide infusion (bottom). Broken line denotes baseline current.

	Discussion

TOP Summary Introduction Materials and methods Results Discussion List of abbreviations References

Through our single cell-electrophysiology analysis, we found that several VSNs were found to respond to more than one chemosignal with opposite polarities of response. This may provide evidence for at least two signaling cascades in a single VSN. This assertion is supported by evidence that more than one G-protein-coupled receptor may be expressed in a single VSN (Martini et al., 2001; Spehr and Leinder-Zufall, 2005). Additionally, attempts to elicit chemosignal-activated currents outside the mating season (April–September) failed (J.H.B., unpublished). One might conjecture that not only size but also components of the cellular function of the VNO (or central projections) may be seasonally regulated.

The fact that Ruthenium Red (RR) did not significantly alter chemosignal-activated currents may suggest that IP₃R3 is not localized to the plasma membrane as has been demonstrated in cilia of olfactory sensory neurons (Fadool and Ache, 1992; Restrepo et al., 1992; Cunningham et al., 1993; Honda et al., 1995; Cadiou et al., 2000). These data, however, fail to reveal whether IP₃R3 is an important member of the signal transduction scaffold. RR is classically used as a blocker of the mitochondrial Ca²⁺ uniporter or of the ryanodine receptor (RyR) located on the ER. It has also been found, when applied extracellularly, to block the IP₃R localized to the dendrite or microvillus of an olfactory or vomeronasal sensory neuron, respectively (Fadool and Ache, 1992; Miyamoto et al., 1992; Taniguchi et al., 1995; Inamura et al., 1997; Taniguchi et al., 2000; Kashiwayanagi et al., 2000). An alternative possibility that must be considered is that the TRPC2/IP₃R3 complex may present a configuration that is inaccessible for pharmacological interception with RR.

This study provides the first evidence that dissociated VSNs from the semi-aquatic turtle, S. odoratus, utilize the phospholipase C (PLC) system in the detection of socially relevant stimuli. A membrane-permeable inhibitor of PLC, U73122, significantly reduced the chemosignal-activated current. These data support the hypothesis that the phosphatidylinositol system underlies the chemosignal response in VSNs. However, it is not clear whether the derivatives of PIP₂, DAG or IP₃, have a direct role in gating the ion channels involved. In guinea pig ileal smooth muscle cells, the activation of the muscarinic receptor-operated cationic current (likely via a TRP channel), is dependent upon PLC, but is not dependent on either IP₃ or DAG (Zholos et al., 2004). PIP₂ may directly modulate the TRP channel in question, as is seen with TRPM5, TRPM7, TRPM7 and TRPV1 (Hilgemann et al., 2001; Liu and Qin, 2005; Chuang et al., 2001; Liu and Liman, 2003; Prescott and Julius, 2003). In these cases, PIP₂ sometimes acts to suppress channel activity. Interestingly, when mutations are made within the PIP₂ binding domain on TRPV1, the channel becomes more sensitive to chemical or thermal stimuli (Prescott and Julius, 2003). In the case of TRPM5 and TRPM8, PIP₂ activates the channel. PIP₂ can reverse the desensitization of TRPM5 (Liu and Liman, 2003). Blocking PIP₂ synthesis inhibits TRPM8 activity (Liu and Qin, 2005). Therefore, PIP₂ has the potential to differentially and directly regulate several members of the TRP ion channel superfamily, and may be directly modulating TRPC2 current in the VNO, either directly affecting the primary receptor potential, or perhaps the formation of a signal complex with IP₃R3.

Using our experimental design, dialysis with the second messengers cAMP, IP₃ or DAG failed to elicit a response in isolated VSNs. Although cAMP did not have an effect, other cyclic nucleotides could be important in a transduction pathway in the musk turtle VNO (Taniguchi et al., 1996). The lack of response with dialyzed messengers could be explained in several ways. First, the whole-cell patch seal was formed on the soma, not on the thin dendritic extension or microvilli. Thus it is possible that the messengers may not have reached a critical concentration near the transduction apparatus in the microvilli (Berghard and Buck, 1996; Ryba and Tirindelli, 1997; Liman et al., 1999; Menco et al., 2001). Contrary to this explanation is that soma dialysis of second messengers by one of the authors has been shown to evoke quite large currents in olfactory sensory neurons of lobster with outer dendrites (primary site of transduction) greater than 1000 µm from the cell body (Fadool and Ache, 1992). This space problem was apparently alleviated in frog VSNs by using flash photolysis of caged IP₃, and selective release of IP₃ only near the microvillus resulted in a series of transient inward currents when the membrane was held at –70 mV (Gjerstad et al., 2003). Second, the VSNs studied here were enzymatically isolated, and may have altered the ability of the VSN to respond to dialyzed second messenger; however, this is less likely because VSNs isolated in the same manner were shown to be responsive to chemosignals, and cells lacking microvilli were not included in the current study. Third, PIP₂ could interact directly with TRPC2 in the musk turtle, bypassing the need for either IP₃ or DAG, as discussed above. Another possibility is that DAG and IP₃ must be presented in tandem for effects to be detected; such synergism in the generation of a non-selective cationic current has been demonstrated in rabbit portal vein myocytes (Albert and Large, 2003). This hypothesis was informally tested here yet the combined presentation of IP₃ and the DAG analogue, SAG, did not elicit currents of either inward or outward polarity. Finally, arachidonic acid, a polyunsaturated acid (PUFA) derived from DAG previously reported to generate chemosignal-like currents in the rat vomeronasal system (Spehr et al., 2002), did not elicit chemosignal-like currents in isolated S. odoratus VSNs but did appear to evoke rapid transients, the function of which is unclear.

Two separate reversal potentials for inward and outward currents were revealed. The majority of chemosignals, with the exception of male urine, were capable of eliciting both polarities of response; hence, most chemosignals did not appear to be stereotypically connected to a particular signal transduction cascade. Male urine, however, may be operating exclusively as a territorial cue, and the receptive pathway for such information may be stereotyped. The outward current, reversing at approximately –30 mV, may be due to the closure of an ion channel of unknown identity. Although a novel transduction mechanism in the musk turtle VNO, such a channel operates in several sensory organs, including the visual system and the mouse VNO (Matesic and Liebman, 1987; Moss et al., 1997). The inward current reversed close to 0 mV, indicating that this current is due to a nonselective cation channel, such as TRPC2. A good future directive would be to explore whether the musk turtle VNO may express a Ca²⁺-activated non-selective (CaNS) cation channel like that found in the hamster (Liman, 2003), or a Ca²⁺-activated chloride channel, similar to that seen in olfactory sensory neurons that would contribute a late-phase amplification of the initial Ca²⁺ current (Kleene, 1993; Lowe and Gold, 1993; Paysan and Breer, 2001).

The interaction between TRPC channels and the IP₃R has been well established (Tang et al., 2001; Yuan et al., 2003; Brann et al., 2002). Here, we sought to demonstrate a role for this interaction in the VNO of the musk turtle. Recent GST-fusion work has shown (Tang et al., 2001) that IP₃R3 and calmodulin bind to a conserved amino acid sequence found on most TRPC channels, including mTRPC2 (mouse TRPC2; amino acids 901–936). mTRPC2 appears to be somewhat unique within the canonical TRP superfamily in that it possesses an additional binding site (amino acids 944–1072) (Tang et al., 2001). We designed a peptide (see Materials and methods) against this sequence to interrupt the binding of IP₃R3 to TRPC2 and analyzed its effect on the chemosignal response over time in musk turtle VSNs, and found that 10 µmol 1^–1 peptide nearly abolished the chemosignal-activated current by 10 min. The use of a peptide to disrupt the interaction between the IP₃R and a TRPC channel has been shown previously; in Xenopus oocytes, suppression of the mTRPC5 current was seen with preinjection of a peptide mimicking the IP₃ binding domain of the IP₃R (Kanki et al., 2001). These results indicate that there is a functional role for the IP₃R in the VNO of the musk turtle. Since dialysis of IP₃ did not elicit a current alone, it is possible that the IP₃R is serving to amplify the initial receptor potential generated by TRPC2, to achieve sensitivity to repeated stimulation with chemosignal, or to modulate seasonality in this species. It is also possible that when IP3R/TRPC2 are in a complex, the IP3 ligand could have less affinity or lack access to the receptor. This later possibility would be consistent with our data that demonstrate a lack of current after IP3 dialysis and failure of an IP3R antagonist (RR) to significantly block chemosignal-activated current.

The experiments presented here demonstrate that the PLC system is required in VSNs from S. odoratus to detect a variety of natural chemical cues, including urine and a reproductive musk known to mediate mating behaviors/courtship (Eisner et al., 1977). This finding is consistent with studies in the rodent (Spehr et al., 2002; Lucas et al., 2003). In addition, it is likely that the TRPC2-IP₃R3 protein–protein interaction previously demonstrated in rodent (Brann et al., 2002) does have a functional role in the chemosignal response of VSNs, as interrupting the interaction resulted in loss of the chemosignal response. These data imply that the connection between the internal Ca²⁺ stores is important to the maintenance of the response in the VNO, and may have a role in the ability of the VNO to respond to chemosignals repetitively without a decrease in action potential firing frequency, a property that is not found in the main olfactory system (Liman and Corey, 1996). Although second messenger dialysis failed to elicit a chemosignal-like current, reversal potential analysis supports the existence of a conductance consistent with a nonspecific cation channel such as TRPC2, the expression of which was found in S. odoratus previously (Murphy et al., 2001). One very interesting result of these studies was that outward currents (as defined at –60 mV) may be due to the closure of an inwardly conducting ion channel. This is not the first report of such a channel in the VNO (Moss et al., 1997; Moss et al., 1998), although it is the first report in the turtle.

	List of abbreviations

TOP Summary Introduction Materials and methods Results Discussion List of abbreviations References

 

AA

arachidonic acid

AOS

accessory olfactory system

ANOVA

analysis of variance

CaM

calmodulin

cAMP

cyclic adenosine monophosphate

CaNS

Ca²⁺-activated non-selective

DAG

diacylglycerol

ER

endoplasmic reticulum

GPCR

G-protein-coupled receptor

IP₃

inositol 1,4,5-trisphosphate

IP₃R

IP₃ receptor

IP₃R3

type 3 IP₃ receptor

MOE

main olfactory epithelium

MOS

main olfactory system

OAG

1-oleoyl-2-acetyl-sn-glycerol

PBS

phosphate buffered saline

PIP₂

phosphatidyl-inositol bis-phosphate

PLC

phospholipase C

PUFA

polyunsaturated fatty acid

R_N

input resistance

RR

Ruthenium Red

RT

room temperature

RyR

ryanodine receptor

SAG

1-stearoyl-2-arachidonoyl-sn-glycerol

SNK

Student–Newman–Keuls

t₀

first exposure to chemosignal

t_n

exposure to chemosignal at time n

t_p

time point

TRPC2

canonical transient receptor potential 2

V_c

command potential

V_h

holding potential

VNO

vomeronasal organ

VSN

vomeronasal sensory neuron

U73122

PLC inhibitor

time constant

	Acknowledgments

 
J.H.B. was supported by a NIH/NIDCD Ruth L. Kirschstein National Research Service Award (NRSA) F31-DC006153 and by a NIH/NIDCD Predoctoral Chemosensory Training Grant T32-DC00044 to the Florida State University. We would like to thank Drs Francis Rose, Mary Mendonca and Craig Guyer for the donation and collection of animals. We would also like to thank Mr Roger Thompson, Mr Chad Thorson, and Ms Randa Perkins for invaluable field assistance.

	Footnotes

 
^* Present address: 920 Fairchild Center, MC 2439, Department of Biological Sciences, Columbia University, New York, NY 10027, USA

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