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The Journal of Neuroscience, August 20, 2003, 23(20):7489-7503
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Connexin35 Mediates Electrical Transmission at Mixed Synapses on Mauthner Cells
A. Pereda,1 J. O'Brien,2 J. I. Nagy,3 F. Bukauskas,1 K. G. V. Davidson,4 N. Kamasawa,4 T. Yasumura,4 andJ. E. Rash4 1Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York 10461, 2Department of Ophthalmology and Visual Science, University of Texas at Houston-Health Science Center, Houston, Texas 77030, 3Department of Physiology, University of Manitoba, Winnipeg R3E 3J7, Canada, and 4Department of Biomedical Sciences, Colorado State University, Fort Collins, Colorado 80523
Abstract
Top
Abstract
Introduction
Auditory afferents terminating as "large myelinated club endings" on goldfish Mauthner cells are identifiable "mixed" (electrical and chemical) synaptic terminals that offer the unique opportunity to correlate physiological properties with biochemical composition and specific ultrastructural features of individual synapses. By combining confocal microscopy and freeze-fracture replica immunogold labeling (FRIL), we demonstrate that gap junctions at these synapses contain connexin35 (Cx35). This connexin is the fish ortholog of the neuron-specific human and mouse connexin36 that is reported to be widely distributed in mammalian brain and to be responsible for electrical coupling between many types of neurons. Similarly, connexin35 was found at gap junctions between neurons in other brain regions, suggesting that connexin35-mediated electrical transmission is common in goldfish brain. Conductance of gap junction channels at large myelinated club endings is known to be dynamically modulated by the activity of their colocalized glutamatergic synapses. We show evidence by confocal microscopy for the presence of the NR1 subunit of the NMDA glutamate receptor subtype, proposed to be a key regulatory element, at these large endings. Furthermore, we also show evidence by FRIL double-immunogold labeling that the NR1 subunit of the NMDA glutamate receptor is present at postsynaptic densities closely associated with gap junction plaques containing Cx35 at mixed synapses across the goldfish hindbrain. Given the widespread distribution of electrical synapses and glutamate receptors, our results suggest that the plastic properties observed at these identifiable junctions may apply to other electrical synapses, including those in mammalian brain.
Key words: gap junction; connexin36; electrical synapse; NMDA; synaptic plasticity; electrical coupling; auditory
Introduction
The cloning of connexin36 (Cx36), a novel neuron-specific gap junction protein in mice, has facilitated studies that indicate the existence of widespread electrical transmission in the mammalian CNS (Condorelli et al., 1998). In situ hybridization revealed that this connexin is widely distributed in mammalian CNS (Condorelli et al., 1998
Because of limited experimental accessibility, very little is known about the plastic properties of electrical synapses in mammals. In contrast, anatomically and physiologically identifiable auditory afferents terminating as large myelinated club endings on the lateral dendrite of the goldfish Mauthner cell (Bartelmez, 1915
A wealth of experimental evidence has shown that gap junctional conductance at large myelinated club endings is enhanced by sustained afferent activity (Yang et al., 1990
An essential step toward investigation of this possibility is to identify which member(s) of the multigene family of gap junction-forming proteins (connexins) is responsible for electrical transmission at large myelinated club endings. By combining confocal microscopy, electrophysiological recording, and FRIL analysis of individual Mauthner cells, we provide evidence that Cx35 (O'Brien et al., 1996
Materials and Methods
Electrophysiological techniques. Intracellular recordings were obtained in vivo from nine VIIth nerve afferents, with recording sites in the root or intracranially, while simultaneous measurements were taken from the Mauthner cell lateral dendrite. Presynaptic recording electrodes were filled with a 2.5 M KCl solution, and their resistances were 35 and 45 M. A second electrode (2.5 M KCl, 4-12 M
Immunochemistry and confocal microscopy. Fish were perfused intracardially with 4% formaldehyde in phosphate buffer (0.12 M at pH 7.4) for 15 min, kept overnight in PBS, and sectioned with a Vibratome (20-50 µm). Sections were rinsed several times with PBS, incubated overnight with anti-Cx36 (Ab298; 1:1000/5000), anti-Cx43 (1:200/2000), or anti-Cx35 (Chemicon MAB3045; 1:200/2000), rinsed in PBS, incubated for 2 hr with Texas Red-conjugated secondary antibody, and rinsed with PBS (antibodies described below). In experiments in which either afferents or Mauthner cells were injected with Neurobiotin, sections were also incubated for 1 hr in streptavidin-conjugated FITC (dilution 1:200) in PBS. The sections were mounted on slides, dehydrated, cleared, covered, and examined under transmitted light or using fluorescence (Leitz Aristoplan) and confocal (Bio-Rad Radiance 2000 laser scanning confocal microscope) microscopes. Control sections were incubated with secondary antibodies in the absence of primary antibodies.
Western blotting and antibodies. For Western blots of tissues, crude goldfish plasma membranes were prepared by differential centrifugation of fresh tissue homogenates of retina and of small portions of goldfish hindbrain containing both of its Mauthner cells. This area (
90 mg of tissue) corresponds to the portion of goldfish hindbrain located below the cerebellum and is delimited by the anterior and posterior aspects of the cerebellar peduncles. Tissues were suspended in a solution containing 0.32 M sucrose, 10 mM Tris-Cl, pH 7.4, 2 mM EGTA, and 5 mM MgCl2 plus 1% (v/v) protease inhibitor mixture (Sigma, St. Louis, MO), and homogenized by sonication for 30 sec with a Branson Sonifier at 35% power. Homogenates were centrifuged 10 min at 1000 x g, and the supernatant was collected and centrifuged for 1 hr at 100,000 x g. The resulting membrane pellets were suspended in homogenization buffer plus 0.5% Nonidet P-40. Protein was assayed by the Bradford technique (Bio-Rad protein assay).
Forty microgram aliquots of membrane protein were dissolved in reducing SDS sample buffer and resolved on 10% SDS-PAGE gels for immunoblots of NR1 or on 12% gels for immunoblots of connexins. Proteins were transferred at 18 V overnight to nitrocellulose membranes for probing of NR1, Cx36, and Cx43 or to polyvinylidenedifluoride membranes for probing of Cx35. Blots were blocked with 5% Carnation nonfat dry milk in TBST (135 mM NaCl, 3 mM KCl, 25 mM Tris-Cl, pH 7.4, 0.05% Tween 20) for 1 hr at room temperature. Primary antibody incubations and washes of membranes were conducted under several different conditions. Mouse anti-NR1 (B-D PharMingen 556308) was diluted to 0.5 µg/ml in TBST plus 5% milk and incubated for 2 hr at room temperature. Mouse anti-Cx35 (Chemicon MAB3045) was diluted to 0.7 µg/ml in hsTBST (500 mM NaCl, 3 mM KCl, 25 mM Tris-Cl, pH 7.4, 0.05% Tween 20) plus 3% nonfat dry milk and incubated for 14 hr at 4°C. Rabbit anti-Cx36 (Ab298) was diluted to 0.7 µg/ml in TBST plus 3% nonfat dry milk and incubated for 14 hr at room temperature. Mouse anti-Cx43 (Chemicon MAB3068) was diluted to 0.8 µg/ml in isTBST (320 mM NaCl, 3 mM KCl, 25 mM Tris-Cl, pH 7.4, 0.05% Tween 20) plus 2% nonfat dry milk and 1% BSA and incubated for 14 hr at 4°C. Blots were washed at room temperature with a TBST solution corresponding to that used for the primary antibody. Washed blots were probed with the appropriate multiple-labeling grade peroxidase-conjugated FAb2 secondary antibodies (Jackson ImmunoResearch) at dilutions from 1:2500-1:5000 with the same blocking agent used for the primary antibody. Washes were done as for the primary antibodies. Bands were detected by chemiluminescence (Pierce SuperSignal). Western blots for a second Cx43 antibody (designated Rebecca, rabbit polyclonal, amino acid sequence 302-319; courtesy of Dr. B. Nicholson, University at Buffalo, Buffalo, NY) were similarly generated using total goldfish brain homogenates.
Freeze-fracture replica immunogold labeling. Both of the two Mauthner cells in each of five goldfish hindbrains were injected with Lucifer yellow and fixed by perfusion after the procedure described above. Brains were dissected and sliced into 150- to 750-µm-thick sections and photographed before FRIL using a Molecular Dynamics Multiprobe 2001 inverted confocal microscope. All thicker slices were resectioned to a uniform 150 µm thickness, infiltrated with 30% glycerol as cryoprotectant to minimize damage during freezing, and frozen by pneumatically damped contact against a liquid nitrogen-cooled copper block (Philips and Boyne, 1984). Samples were freeze fractured and replicated in a JEOL/RMC RFD 9010C freeze-fracture device, removed, and while still frozen, embedded in Lexan plastic film on a gold "index" grid. Samples were thawed, photography mapped by confocal microscopy, and cleaned by vigorous washing for 24-29 hr in 2.5% SDS detergent (Fujimoto, 1995
Results
Specificity of antibodies
Two antibodies were used to label Cx35 in goldfish. As reported previously (Rash et al., 2000Monoclonal anti-Cx35 (Chemicon MAB3045) was generated against a recombinant fusion protein containing the entire intracellular loop of perch Cx35. The specificities of both polyclonal Ab298 and monoclonal anti-Cx35 were confirmed with Western blots of recombinant perch Cx35 and Cx34.7 proteins (Fig. 1A,B). The glutathione S-transferase (GST) fusion proteins used were generated by cloning the intracellular loop and C-terminal tail coding sequences of perch Cx35 and perch Cx34.7 into pET42 (J. O'Brien, unpublished results). The constructs were expressed in Escherichia coli strain BL21(DE3), and Western blots were performed on crude lysates of cells after 1 hr of induction. Approximately 0.5 µg of total protein was loaded per lane. Figure 1, A and B, shows that both antibodies were specific for Cx35 and did not recognize the corresponding portion of Cx34.7.
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Figure 1. Western blot analyses with various anti-connexin and anti-glutamate receptor antibodies. A, Polyclonal anti-Cx36 Ab298 recognizes a complex of bands at 31-33 kDa in goldfish retina (Ret) and hindbrain (Brn) and bands at 60-70 kDa possibly representing a dimer form of Cx35 (left). In bacterial extracts (right), Ab298 detects the 36 kDa Cx35 C-terminal GST fusion protein (35CT) and its lower molecular weight cleavage products, but not Cx34.7 C-terminal fusion protein (34.7CT) or GST alone. B, Monoclonal anti-Cx35 also detects the 31-33 kDa bands in hindbrain and retina (left). In crude bacterial extracts (right), only the Cx35 intracellular loop GST fusion protein is recognized. C, D, Both monoclonal (C) and polyclonal (D) anti-Cx43 antibodies recognize two to three prominent bands at 40-44 kDa in goldfish hindbrain. These bands comigrate with Cx43 from rat brain (D), and both membranes (lanes a) and supernatant fractions (lanes b) contain Cx43. E, Monoclonal anti-NR1 recognizes a single 100 kDa band in retina and hindbrain.
All of the antibodies used in this study labeled appropriate bands in Western blots of goldfish tissues (Fig. 1). Both Ab298 and MAB3045 recognized the same bands in goldfish hindbrain and retina. Because these antibodies recognize epitopes in different cytoplasmic domains of Cx35, this provides further evidence that antibody labeling was specific. The monoclonal anti-NR1 used for FRIL immunolabeling (B-D PharMingen 556308) recognized a single 100 kDa band in retina and hindbrain. A second antibody directed against the NR1 subunit of the NMDA receptor of the electric fish Apteronotus (AptNR1; polyclonal; amino acid sequence 844-901) was used for light microscopic immunolabeling. Previous immunoblotting demonstrated the specificity of this antibody for teleost NMDA-NR1 (Berman et al., 2001
Identification of large myelinated club endings
Mauthner cells were intracellularly injected with either Neurobiotin or Lucifer yellow to facilitate cell identification during confocal analysis and FRIL investigations. Figure 2A illustrates one of these cells injected with Lucifer yellow, allowing visualization of its most relevant portions. The large myelinated club endings, henceforth referred to as club endings, constitute a special type of auditory afferent terminating as unramified, single terminals on distal portions of the lateral dendrite (Bartelmez, 1915
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Figure 2. Anatomical and physiological identification of large myelinated club endings. A, Confocal image of Mauthner cell and its axon cap, soma, and lateral dendrite visualized after intracellular injection of Lucifer yellow. Club endings are segregated to the distal portion of the lateral dendrite (boxed area), and these endings exhibit faint labeling by dye transfer from the dendrite. B, Distal portion of the lateral dendrite (LD) labeled by peroxidase-DAB reaction after intracellular injection with Neurobiotin tracer. Some club ending afferents are labeled as a result of gap junction-mediated tracer transfer to presynaptic terminals. C, Normarski optics view of the lateral dendrite surface where club endings are readily identified among other terminals by their large size (dotted circle). D, Experimental design for intracranial simultaneous recordings. Club endings forming mixed synapses (asterisk) were penetrated while simultaneously recording from a Mauthner cell lateral dendrite. E, Mixed synaptic transmission at club endings demonstrated by intracranial simultaneous recordings. A presynaptic depolarizing pulse triggers a presynaptic action potential (Pre spike) and depolarization. Both the spike and subthreshold pulse depolarization are recorded as the electrical component in the postsynaptic lateral dendrite. A glutamate-mediated slower response (chemical, yellow area) follows the electrical potential produced the presynaptic spike.
Club endings have characteristic physiological properties, allowing correlation of physiology with ultrastructural features of chemical and gap junctional transmission at these contacts. Presynaptic action potentials at these terminals evoke mixed excitatory synaptic responses in the lateral dendrite. These responses are composed of a fast electrical potential followed by a chemical EPSP mediated by glutamate (Furshpan, 1964
Confocal microscopy revealed abundant Cx35 at large myelinated club endings
To determine whether Cx35 is present at club endings, we performed experiments using a previously characterized anti-Cx36 antibody (Rash et al., 2001
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Figure 3. Laser scanning confocal immunofluorescence showing Cx35 at large myelinated club endings with polyclonal anti-Cx36 antibody Ab298. A, Confocal projection (30 sections; 20 µm) of the distal portion of the Mauthner cell lateral dendrite, which was physiologically identified and intracellularly injected with Neurobiotin for cell identification during confocal microscopy. Cx35 was visualized by Texas Red secondary antibody (red), and Neurobiotin was visualized by streptavidin FITC (green). B, Stack of three z-sections (2 µm) through the surface of the Mauthner cell lateral dendrite. Several club endings, identified by their large size and delineated by red immunofluorescence, exhibit multiple sites of punctate or patchy labeling for Cx35 (magnified in inset, asterisk). C, Lateral view of club ending showing restriction of labeling at lateral dendrite-club ending interface. D, Laser scanning confocal immunofluorescence showing Cx35 at large myelinated club endings using monoclonal anti-Cx35 antibody. Images derived from three confocal z-sections (2 µm) through the surface of the distal portion of a Mauthner cell lateral dendrite show multiple labeled club endings.
Club endings are not the only mixed synaptic contacts that terminate on Mauthner cells. Immunofluorescence labeling with anti-Cx35 and anti-Cx36 antibodies was also observed in other areas of Mauthner cells, including the soma (Fig. 4A), proximal portion of the lateral dendrite (Fig. 4B), and the ventral dendrite (data not shown). The intense labeling observed at the proximal portion of the lateral dendrite suggests that other octavolateralis synaptic contacts contain gap junctions composed of Cx35, possibly including anterior eighth nerve and lateral line afferents that are known to contact the lateral dendrite more proximally (Zottoli and Van Horne, 1983
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Figure 4. Laser scanning confocal immunofluorescence of Cx35 associated with Mauthner cell somata and proximal dendrite. A, View of the Mauthner cell soma showing intense labeling for Cx35 with polyclonal Ab298 (red). The Mauthner cell was injected with Neurobiotin (green) as in Figure 3. Labeling is seen on both soma and small somatic dendritic processes (inset). Small "cap dendrites" projecting inside the axon cap (arrowhead) are also faintly labeled with Neurobiotin. B, View of a most proximal region of the lateral dendrite where a club ending in the boxed area (magnified in inset, arrowhead) appears among other terminals of smaller size, likely corresponding to anterior eighth nerve or lateral line inputs to the Mauthner cell, or both. C-E, Labeling of Cx35 (Ab298) associated with neurons in various regions of goldfish hindbrain. Image shows a confocal projection of large vestibulospinal (C) and two reticulospinal (D, E) neurons. Punctate labeling is seen dispersed throughout the surface of these neurons.
Intense punctate labeling for Cx35 also was found in large vestibulospinal neurons (Fig. 4C) located in the vicinity of the tip of the Mauthner cell lateral dendrite. Vestibulospinal neurons are known to receive multiple mixed synaptic inputs from eighth nerve afferents. In this instance, >300 puncta are visible on the surface of the vestibulospinal neuron. A similar labeling pattern was observed in other hindbrain neurons, including large reticulospinal neurons located in the vicinity of the Mauthner cell ventral dendrite (Fig. 4D,E). On the basis of size and separation of puncta and size of nerve terminals on vestibulospinal and reticulospinal neurons, each punctum is presumed to represent the gap junctions of a single nerve terminal.
FRIL identification of Mauthner cells
Identification of club endings using the FRIL method was facilitated by combining electrophysiological and anatomical techniques. Physiologically identified Mauthner cells were injected with Lucifer yellow, the fish were perfusion fixed, and the brains were sectioned for FRIL. Tissue containing the distal lateral dendrite of the Mauthner cells was identified by fluorescence microscopy, frozen, fractured and replicated, and immunogold labeled by the FRIL technique. Before SDS washing and immunogold labeling, a photo map revealing the position of the dendrite relative to the grid openings was obtained by confocal microscopy (Fig. 5A). This procedure allowed us to locate the Mauthner cell lateral dendrite and to identify club endings in the replica.
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Figure 5. FRIL images of Cx35 localization at gap junctions between a Mauthner cell lateral dendrite and large myelinated club endings. A, Confocal micrograph of a FRIL replica containing a Lucifer yellow-injected Mauthner cell bonded to a gold index grid. Fracture plane traverses obliquely through the Mauthner cell, revealing views from club ending toward Mauthner cell (B, C) and from Mauthner cell toward club ending (Fig. 7). Yellow arrow indicates approximate location of club ending illustrated in B and C. At this light microscopic magnification, the yellow arrowhead covers
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Figure 7. FRIL double labeling of Cx35 in gap junction plaques within the presynaptic membrane and of NR1 subunit of NMDA glutamate receptors in nearby IMPs in postsynaptic particle clusters (designated PSDs) in the postsynaptic membrane. A, Gap junctions and PSDs in postsynaptic membrane of a Mauthner cell. Cx35 labeling (Ab298) is approximately as dense in the presynaptic membrane as in postsynaptic membranes elsewhere in the same cell (Fig. 5C). B, Simultaneous double labeling for Cx35 (6 nm gold beads) and for glutamate receptor NR1 (18 nm gold beads) in a PSD of an identified Mauthner cell club ending in a different replica. The PSD (yellow) contains 10 nm IMPs, some of which were damaged by scraping during the fracturing event (right side of PSD). C, Four of five Cx35-labeled gap junctions (10 nm gold beads) in a small portion of a club ending on the same Mauthner cell as shown in Figures 5 and 7A. A nearby small PSD is labeled for NR1 (18 nm gold bead). Because membrane continuity was interrupted, identification as a club ending was on the basis of synapse size, number of closely spaced gap junctions, and FRIL mapping criteria. D, NR1-labeled PSD in a non-club ending synapse in the same Mauthner cell illustrated in Figures 5 and 7A. As above, Cx35 is labeled by 10 nm gold (none present here), whereas NR1 is labeled by 6 nm (arrow) and 18 nm gold beads. The PSD is shown in stereoscopic (left pair) and reverse stereoscopic perspective (right pair). In reverse stereoscopic perspective, the smallest gold beads (6 nm) are readily discerned as if suspended above the replicated 6-10 nm IMPs. E, Laser scanning immunofluorescence showing NR1 at large myelinated club endings with anti-AptNR1 antibody. The image represents a stack of three z-sections (2 µm) through the surface of the M-cell lateral dendrite. Two club endings, identified by their large size and location, are delineated by green immunofluorescence. Each exhibits multiple punctate labeling that, in contrast with Cx35 (Fig. 3), is restricted to the perimeter of the contacts.
By FRIL, Mauthner cells, club endings, other uninjected neurons, dendrites, nerve terminals, astrocytes, oligodendrocytes, and vascular endothelial cells were identified on the basis of established freeze-fracture criteria (Harris and Landis, 1986
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Figure 6. Basis for FRIL identification of membrane proteins. A, B, Diagram showing portions of a mixed synapse before (A) and after freeze fracturing and immunogold labeling (B). The fracture plane (A, green line) separates connexons at the point of contact in the extracellular space, leaving either intramembrane particles (IMPs) in the P-face (P) or arrays of pits in the E-face (E). All gap junctions exposed by fracturing are separated into two hemiplaques; one hemiplaque remains associated with each of the two freeze-fractured cells. Whether E-face pits or P-face particles are visualized by FRIL, antibody labeling of connexins and secondary immunogold beads bind only to connexins in the hemiplaque of the cell with a cytoplasmic membrane leaflet that remains beneath the replica. For E-face images, all connexons of the upper cell are removed, but connexons remain within the unsplit membrane of the underlying, nonvisualized cell. For intramembrane proteins other than connexins, however, immunogold labeling sites are present only beneath replicated IMPs, on either E-faces or P-faces. Proteins comprising PSDs of glutamatergic synapses consist of distinctive clusters of E-face IMPs (B), which are available for immunogold labeling of determinants exposed in the residual extracellular space. C, Diagram of fracture plane through an individual Mauthner cell, including views from the presynaptic side toward the postsynaptic side (top left) and from the postsynaptic side toward the presynaptic side (bottom right). Glutamate receptor PSDs are clusters of E-face IMPs that are immunogold labeled on their extracellular determinants.
A total of 85 gap junctions (Fig. 5B, delineated in red) were identified in one contiguous portion of the E-face of one of the many club endings, and an additional 20 gap junctions were clustered in the postsynaptic membrane underlying the same club ending (Fig. 5B, delineated in blue at bottom left corner). The combined value of 100+ gap junctions is in the middle range of the number of junctional plaques within individual club endings (Tuttle et al., 1986
In FRIL, as in conventional freeze-fracture replicas (Rash et al., 2001
Cx35 is present presynpatically and postsynaptically at large myelinated club endings
To establish ultrastructurally that Cx35 is localized to gap junctions, and to determine whether the same connexin is present on both the club ending and Mauthner cell sides of gap junction plaques, we used FRIL to examine both sides of individual obliquely fractured Mauthner cells that have been labeled using Ab298. The fracture plane in the replica illustrated in Figures 5 and 7 passed obliquely through one Mauthner cell lateral dendrite, thus exposing both presynaptic and postsynaptic views of two different club endings located on opposite sides of the same lateral dendrite (represented diagrammatically in Fig. 6C and illustrated in Figs. 5B,C, and Fig. 7A). Thus, the two FRIL views of synapses on the same Mauthner cell reveal that Cx35 labeling occurred on connexons within the postsynaptic plasma membranes (Fig. 5B,C), as well as within the presynaptic plasma membrane (Fig. 7; represented diagrammatically in Fig. 6A,B), thereby demonstrating that both sides of the gap junctions formed between Mauthner cell lateral dendrites and club endings contain Cx35.Postsynaptic densities at large myelinated club endings contain NMDA receptors Pharmacological and immunochemical data suggest that chemical transmission at club endings is mediated by glutamate (Sur et al., 1994
To confirm that NR1 is present at club endings, we performed experiments using a previously characterized teleost anti-NR1 antibody (n = 3), directed against the NR1 subunit of the electric fish Apteronotus (Berman et al., 2001
FRIL confirms that connexin35 and NR1 are widespread among neurons
Immunogold labeling for Cx35 was not restricted to club endings but was also found in other mixed synapses located in the proximity of Mauthner cells. In a sample of goldfish brain examined for Cx35 with MAB3045 (monoclonal anti-perch Cx35), neuronal gap junctions were labeled with 6, 18, and 20 nm gold beads (Fig. 8). The presence of three sizes of immunogold beads provides three different confirmations of labeling specificity of this monoclonal antibody. Immunogold beads were found restricted to neuronal gap junctions (Fig. 8B).
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Figure 8. FRIL labeling of Cx35 in gap junctions at mixed synapses of unidentified neurons in goldfish hindbrain. A, Freeze-fracture view of the postsynaptic E-face and of two nerve terminal P-faces (NT1, NT2). Gap junctions are labeled with three sizes of gold beads. B, Higher magnification view of left boxed area in A, shown as stereoscopic images (left pair) and reverse stereoscopic images (right pair). Cx35 is labeled with 19 6 nm gold beads (arrow), 3 18 nm gold beads, and 3 20 nm gold beads. The field also contains a small unlabeled gap junction (arrowhead). C, Area of Mauthner cell with closely adherent astrocyte processes. Astrocyte gap junctions were not labeled for Cx35.
Although neuronal gap junctions were heavily labeled by the several antibodies to Cx35, no gap junctions between any other non-neuronal cell types were labeled for Cx35. For example, closely adjacent astrocyte gap junctions were unlabeled (Fig. 8 A, C). In a higher magnification stereoscopic image of one of the immunogold-labeled neuronal gap junctions (Fig. 8 B, left pair), and in its intaglio image (Fig. 8 B, right pair), 19 6 nm gold beads (arrow), 3 18 nm gold beads, and 3 20 nm gold beads are seen, all representing labeling for Cx35. This image also demonstrates higher labeling efficiencies for small gold beads and lower labeling efficiency for large immunogold beads (Rash et al., 2001
A third anti-Cx36 antibody (Zymed Ab-6300) also was found to be effective for identifying goldfish neuronal gap junctions by FRIL. In two mixed synapses on an unidentified neuronal process in close proximity to a mapped Mauthner cell, one gap junction was labeled by five 20 nm immunogold beads (Fig. 9A, large inset), and one nearby small gap junction was unlabeled (small inset). The cluster of E-face IMPs in the bottom right corner resembles glutamate receptor-containing PSDs (Fig. 7). Consequently double labeling for NR1 and Cx35 was evaluated in other types of neurons. Double labeling for Cx35 and NR1 in hindbrain regions revealed NR1 labeling in five mixed synapses in five unidentified neurons. As in the case of Mauthner cell mixed synapses (Fig. 7), these contained Cx35 (30 nm gold) in their gap junctions and NR1 receptors (10 nm gold) in their closely associated E-face PSDs (Fig. 9B). Additional glutamate receptor PSDs were found at purely chemical synapses (data not shown).
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Figure 9. FRIL single labeling for Cx35 (A) and double labeling for Cx35 and NR1 (B) in mixed synapses between unidentified neurons in goldfish hindbrain. A, Two gap junctions (inscribed areas, magnified in inset at top right) linking nerve terminals (NT1, NT2) to postsynaptic membrane. One gap junction is unlabeled (top inset), and the other (bottom inset) is labeled by five 20 nm gold beads. Also evident is a PSD at the bottom right. B, Double-labeled mixed synapse with NR1 in the PSD labeled by 10 nm gold beads (white arrows) and the gap junction labeled for Cx35 by 20 nm gold beads (black arrow). Immunogold beads up to 50 nm from the margins of gap junctions presumably represent labeling of connexins in dissolving membrane blebs, as illustrated in Rash and Yasumura (1999
Connexin43 labeling is restricted to astrocytic gap junctions
Immunofluorescence localization of Cx43 by confocal microscopy was conducted to investigate whether Cx43 contributes to electrical transmission at club endings, as suggested previously (Yox et al., 1990
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Figure 10. Localization of Cx43 near Mauthner cell lateral dendrites. A, Presynaptic and postsynaptic simultaneous unitary recording (A) from the labeled club ending and dendrite illustrated in B. The presynaptic electrode was inserted into afferent fibers of the posterior eighth nerve root and therefore differs from the recording in Figure 2 E, where the presynaptic electrode was inserted in the presynaptic terminal, allowing detection of subthreshold responses. No chemical component was detected at this contact, a common observation at these terminals during unitary recordings (Lin and Faber, 1988
In samples of goldfish brain labeled for Cx43 (monoclonal) with 20 nm immunogold beads and examined by FRIL, >100 Cx43-containing gap junctions were detected. All of the labeled gap junctions were within astrocyte plasma membrane (Fig. 10C). Astrocytes were identified by the presence of GFAP filaments in their cytoplasms (Fig. 10C) and by a characteristic high density of dispersed IMPs in their E-faces (Rash et al., 1997
In the same Cx43-labeled FRIL replica, neuronal gap junctions were found at mixed synapses, but none were labeled for Cx43 (Fig. 10D). This close juxtaposition of Cx43-labeled astrocyte gap junctions and unlabeled neuronal gap junctions is compelling evidence that Cx43 is not present in detectable amounts in neuronal gap junctions in goldfish hindbrain.
Discussion
Gap junctions at large myelinated club endings contain Cx35
Studies of large myelinated club endings led to early insights into the mechanisms of electrical transmission between neurons (Bennett at al., 1963Confocal immunofluorescence microscopy revealed abundant Cx35 in Mauthner cell/club ending synapses. These synapses were identified by their uniquely large size and distinctive subcellular location on lateral dendrites, as well by confocal grid-mapping of Mauthner cell lateral dendrites that had been injected with Lucifer yellow during intracellular recordings. Immunofluorescence mapping followed by FRIL revealed abundant Cx35 in gap junction plaques at these club ending synapses. Thus, the ability to combine physiological and ultrastructural analysis at club endings on Mauthner cells provides a powerful system to explore detailed mechanisms of electrical transmission in the vertebrate brain.
The intensity of labeling for Cx35 observed by confocal microscopy and the presence of this connexin in virtually every gap junction plaque as demonstrated by FRIL indicates that Cx35 is a major component of these junctions and thus primarily responsible for electrical transmission at club endings. Moreover, our identification of Cx35 on both the Mauthner cell and club ending side of gap junctions between these structures suggests that electrical transmission at club ending synapses may occur through homotypic gap junction channels. Interestingly, and in contrast with FRIL labeling with Ab298 antibody, we did not observe postsynaptic labeling of gap junctions in club endings with the monoclonal Cx35 antibody (MAB3045). This may reflect the limited number of views seen using this antibody, differences in labeling efficiency of epitopes exposed in presynaptic versus postsynaptic cytoplasm, or differences between presynaptic and postsynaptic connexins. Nevertheless, we do not exclude that additional connexins may be present at club ending gap junction plaques and that these may be expressed differentially.
By combining quantitative analysis of the average number of connexons in individual club endings (Tuttle et al., 1986
Anti-Cx43 antibodies injected into Mauthner cells were reported to alter electrical coupling of these cells, leading to the conclusion that Cx43 is responsible for electrical transmission at club endings (Yox et al., 1990
Cx35-mediated electrical transmission is widespread in the goldfish hindbrain
Confocal microscopy revealed that Cx35 labeling was not restricted to club endings; intense punctate staining was also observed at the proximal portion of Mauthner cell lateral dendrite, soma, and ventral dendrites. Thus, other electrical synapses on Mauthner cells, presumably arising from auditory afferents, anterior eighth nerve, and lateral line inputs, also contain Cx35. In addition, Cx35 labeling was observed in other hindbrain neurons known to receive electrically mediated inputs, including large vestibulospinal (Richter et al., 1975Activity-dependent plasticity of electrical synapses
Gap junctions located at club endings are dramatically influenced by cellular activity. High-frequency stimulation of these afferents evokes a long-lasting enhancement of electrical transmission. Such activity-dependent modification of the strength of electrical transmission seems to depend on functional interactions with neighboring, colocalized glutamatergic synapses. Thus, it has been proposed that NMDA receptors (Yang et al., 1990Implications for electrical transmission in mammalian CNS
The functional interactions of gap junctions and glutamatergic receptors may also occur at mammalian mixed synapses, which are more prevalent than generally recognized. Using the same ultrastructural criteria for identification of neuronal elements as applied in the current study, conventional freeze-fracture studies revealed that mixed synapses are abundant throughout the rat spinal cord, comprising 3-10% of all synapses on both interneurons and motor neurons (Rash et al., 1996Mixed synapses also have been identified in inferior olive, cortex, lateral vestibular nucleus, retina, and hippocampus (Sloper, 1972
Because activity-driven interactions between chemical and electrical synapses at club endings seem to occur postsynaptically via PSD-mediated signaling (Pereda et al., 1998
Footnotes
Received Sep 10, 2002; revised June 19, 2003; accepted June 24, 2003.This work was supported by National Institutes of Health Grants DC03186 (A.P.), EY 12857 (J.O.), and NS44010/NS39040/NS44395 (J.E.R.) and the Canadian Institute of Health Research of Canada (J.I.N.). We thank R. Rodriguez, A. Bukauskiene C. Castillo, and M. Smith for immunochemical work; S. Curti for his contribution to the intracranial simultaneous recordings; B. Nicholson for providing the Cx43 Rebecca antibody, and I. Fischer for help with its Western blot; and R. Dunn and L. Maler for providing the AptNR1 antibody. We also thank P. Castillo, D. S. Spray, F. E. Dudek and M. V. L. Bennett for critically reading this manuscript. We are particularly indebted to M. Cammer and the Analytical Image Facility at the Albert Einstein College of Medicine for outstanding confocal microscopy assistance. We also thank D. Pettit for confocal assistance and B. Magnie for assistance with Photoshop images.
Correspondence should be addressed to A. Pereda, Department of Neuroscience, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10465. E-mail: apereda{at}aecom.yu.edu.
Copyright © 2003 Society for Neuroscience 0270-6474/03/237489-15$15.00/0
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