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A O Willows

Publications and source records attributed to A O Willows.

At least 19 recordsLinked to original sources
PubMed2000

Immunocytochemical localization of pedal peptide in the central nervous system of the gastropod mollusc Tritonia diomedea.

Tritonia pedal ganglion peptides (TPeps) are a trio of pentadecapeptides isolated from the brain of the nudibranch Tritonia diomedea. TPeps have been shown both to increase the beating rate of ciliated cells of Tritonia and to accelerate heart contractions in the mollusc Clione limacina. Here we examine the immunocytochemical distribution of TPeps in the Tritonia central nervous system. We found the brain and buccal ganglia to be rich sources of TPep immunoreactivity. Specific cells in both structures, some of them previously identified, were immunoreactive. Moreover, immunoreactive fibers were seen connecting ganglia and exiting almost all the major nerves. In the brain, we found that the paired, ciliated statocysts apparently receive TPep innervation. In addition, we observed unstained cell bodies in each buccal ganglion with extensive TPep immunoreactive projections surrounding their somata and primary neurites. Similar projections were not observed in the brain. We also compared the TPep immunoreactivity with that of SCP(b) in the buccal ganglia. We observed many neurons and processes that were immunoreactive to both peptides. One neuron that contains both TPep- and SCP(b)-like peptides (B12) has an identified role in the Tritonia feeding network. Together, these findings suggest that TPeps may play an active role in the central nervous system of Tritonia as neurotransmitters modulating orientation, swimming, and feeding.

Animals↗
PubMed2000

Computer-assisted visualizations of neural networks: expanding the field of view using seamless confocal montaging.

Microscopic analysis of anatomic relationships within the neural networks of adult and developing tissues often requires sampling large spatial regions of neuronal architecture. To accomplish this, there are two common imaging approaches: (1) image the entire area at once with low spatial resolution; or (2) image small sections at higher magnification/resolution and then join the sections back together by mosaic reconstruction (photomontaging). Low magnification imaging is relatively rapid to perform, resulting in a visualization that encompasses a large field of view with an extended depth of field. However, for fluorescence microscopy, low magnification visualizations are often plagued by poor spatial resolution. High magnification imaging possesses superior spatial resolution, but it produces an image with limited depth of field. When creating a larger field of view, the final image is also fragmented at the boundaries where multiple images are stitched together. Using confocal microscopy as well as features of common image processing programs, we outline a new method to transform individual, spatially contiguous z-series into a montage with a seamless field of view and an extended depth of field. In addition, we show that the manual alignment of images our method requires does not introduce significant errors into the final image. We illustrate our method for visualizing neural networks using tissues from the adult gastropod mollusc, Tritonia diomedea, and the developing zebrafish, Danio rerio.

Animals↗
PubMed1999

Differential effects of serotonergic and peptidergic cardioexcitatory neurons on the heart activity in the pteropod mollusc, Clione limacina.

A group of four cardioexcitatory neurons has been identified in the intestinal ganglia of the mollusc Clione limacina. Relatively weak stimulation of the intestinal neurons induced auricle contractions only, while strong stimulation produced initial auricle contractions followed by full-cycle auricle-ventricle contractions. Intestinal cardioexcitatory neurons probably utilized as their transmitter a peptide similar to Tritonia pedal peptide--they showed pedal peptide-like immunoreactivity, and their effects were mimicked by application of the exogenous pedal peptide. The pedal cardioexcitatory neuron was found to produce strong excitatory effects only on the ventricle contractions. Its stimulation induced ventricle contractions in the quiescent heart or significantly accelerated the rate of ventricle contractions in the rhythmically active heart. The pedal cardioexcitatory neuron apparently utilized serotonin as a neurotransmitter, based upon serotonin immunoreactivity, blocking effect of serotonin antagonists mianserin and methysergide, and the observation that exogenous serotonin mimicked its effect. A dense network of pedal peptide-like immunoreactivity was found both in the auricle and ventricle tissue. Serotonin immunoreactivity was densely present in the ventricle, while the auricle contained only a separate serotonin-immunoreactive unbranched axon. Thus, there are two separate groups of central cardioexcitatory neurons with different effects on heart activity, which together might provide a complex cardio-regulatory function in Clione.

Animals↗
PubMed1999

Serotonin inhibits ciliary transport in esophagus of the nudibranch mollusk Tritonia diomedea.

Both serotonin and the molluskan pedal neuropeptides (TPEPs) cause increased ciliary beating rate of cells of the foot epithelium of the nudibranch mollusk, Tritonia diomedea. Here we compared responses of the ciliated epithelium of the esophagus with that of the foot, and report fundamental differences. Serotonin reduces the ciliary transport rate of the esophagus. We find also that the serotonin driven inhibition of esophagus is blocked and the excitation of foot epithelium is reduced by the serotonin receptor blocker ketanserin. On the contrary, ergometrine completely blocked the serotonin effect in the esophagus, and does not block the serotonin effect in the foot. Neither the TPEP driven excitation of ciliated cells of the foot nor that of the esophagus is blocked by ketanserin and ergometrine. Clearly, serotonin and TPEP regulation of different ciliated epithelia involve different receptors. Thus, mechanisms of serotonin control of different ciliated epithelia in the same animal are apparently fundamentally different, and unlike responses in all previous reports, 5HT here inhibits a ciliated epihelium.

Animals↗
PubMed1997

Modulation of ciliary beat frequency by neuropeptides from identified molluscan neurons.

Prior work in the nudibranch Tritonia diomedea indicated that certain identifiable pedal ganglion neurons (Pd5 and 6) innervating the foot synthesize three novel peptides (TPeps) that resemble Pedal peptide (Pep) identified in the sea hare Aplysia californica. We report here that when TPeps are applied directly to isolated ciliated patches of Tritonia diomedea foot epithelium, there is an increase in ciliary beating that normally drives locomotion. Exposure to TPeps also increases the ciliary beat frequency of cells isolated from the pedal epithelium, suggesting that the observed ciliomotor effects are direct and not mediated by intervening cells. Antibodies to TPep bind to specific cells of the brain and foot and to ciliated peripheral tissues in Tritonia diomedea and in the pulmonate gastropod Lymnaea stagnalis. We suggest, therefore, that TPeps may regulate the activity of ciliated cells responsible for pedal locomotion and other functions in gastropod molluscs.

Animals↗
PubMed1996

Function of identified nerves in orientation to water flow in Tritonia diomedea.

We determined which sensory and motor nerves mediate orientation to flow in the marine slug Tritonia diomedea, and tested the hypothesis that the slug orients to water flow by comparing the intensities of water flow stimulation on each side of its body. Lesion experiments revealed which nerves carried information necessary for flow orientation. The lateral branches of Cerebral Nerve #2 were the only cerebral nerves necessary for flow orientation. Cutting all cerebral nerves except the lateral branches of Cerebral Nerve #2 did not eliminate flow orientation. Thus, the lateral branches of Cerebral Nerve #2 were both necessary and sufficient (among the cerebral nerves) for flow orientation. Denervation of one side of the head by cutting Cerebral Nerves #1-4 on one side did not eliminate normal flow orientation. We have revised our model of how Tritonia diomedea orients to flow to allow for this unilateral determination of flow direction. Unilaterally cutting Pedal Nerve #3, which contains many pedal motor axons, reduced turning toward that side, but did not affect final orientation to flow. The ability to detect flow direction was not compromised by the inability to initially turn towards flow.

Animals↗
PubMed1996

Purification and sequencing of neuropeptides from identified neurons in the marine mollusc, Tritonia.

Neuropeptides were characterized in two similar identified neurons termed pedal 5 and 6 (Pd5 and Pd6). Both neurons appear white, a characteristic of peptidergic neurons, and send peripheral axons down several nerves that innervate the foot and control locomotion. Gel electrophoresis of neurons incubated with labeled amino acids indicated that individually dissected Pd5 and Pd6 neurons synthesized peptide precursors of the same size and processed them in parallel. Using HPLC, several absorbance peaks that had retention times typical of peptides were identified that were specific to extracts of Pd5 and Pd6. Three peptides were purified from extracts of many pooled Pd5 and Pd6 neurons. The complete sequences of two 15-amino acid peptides were obtained and the sequence of a third 15-amino acid peptide was inferred from the partial sequence of an apparent processing intermediate. Each of the three peptides show sequence homology to Aplysia pedal peptide (Pep). HPLC of neurons incubated with labeled amino acids demonstrated that Pd5 and Pd6 each synthesized all three sequenced peptides.

Amino Acid Sequence↗
PubMed1992

Evidence for homologous peptidergic neurons in the buccal ganglia of diverse nudibranch mollusks.

The buccal ganglia of seven nudibranches (Aeolidia papillosa, Armina californica, Dirona albolineata, D. picta, Hermissenda crassicornis, Melibe leonina, and Tritonia diomedea) were examined to explore possible homologies between large cells that reacted with antibodies directed against small cardioactive peptide B (SCPB). The buccal ganglion of each species possessed a pair of large, dorsal-lateral, whitish neurons that contained an SCPB-like peptide. We refer to these neurons as the SLB (SCPB-immunoreactive Large Buccal) cells. In all species examined, the SLB cells project out the gastroesophageal nerves and appear to innervate the esophagus. In each species, an apparent rhythmic feeding motor program (FMP) was observed by intracellular recording from both SLB neurons and other neurons in isolated preparations of the buccal ganglia. SLB cells often fire at a high frequency, and usually burst in a specific phase relation to the FMP activity. Stimulation of SLB cells enhances expression of the feeding motor program, either by potentiating existing activity or eliciting the FMP in quiescent preparations. Finally, perfusion of isolated buccal ganglia with SCPB excites the SLB cells and activates FMPs. Thus, both the immunohistochemical and electrophysiological data suggest that the SLB cells within three suborders of the opisthobranchia (Dendronotacea, Arminacea, and Aeolidacea) are homologous. A comparison of our data with previously published studies indicates that SLB cell homologs may exist in other gastropods as well.

Animals↗
PubMed1992

Water-flow sensitive pedal neurons in Tritonia: role in rheotaxis.

We have identified 13 pairs of neurons in the pedal ganglia of the marine nudibranch slug Tritonia diomedea that responded tonically and/or phasically to water-flow directed at the rhinophore sheaths and oral veil tips. Most of the neurons responded equally to inputs from either side of the body, but 6 pairs responded with greater intensity to ipsilateral water-flow stimuli. When stimulated intracellularly in a semi-intact, whole-animal preparation, 4 of these 6 pairs of neurons caused ipsilateral movements that may turn the animal towards that side. These observations suggest a role for these current-sensitive neurons in the previously described orientation to water-currents in Tritonia diomedea.

Action Potentials↗
PubMed1991

An identifiable molluscan neuron responds to changes in earth-strength magnetic fields.

Diverse animals can orient using geomagnetic cues, but little is known about the neurophysiological mechanisms that underlie magnetic field detection. The marine mollusc Tritonia diomedea (Bergh) has a magnetic sense and its nervous system is amenable to cellular-level electrophysiological analysis. In a semi-intact whole-animal preparation, intracellular recordings from the large, visually identifiable neurons left pedal 5 (LPe5) and right pedal 5 (RPe5) in the brain of Tritonia revealed enhanced electrical activity in response to changes in ambient earth-strength magnetic fields. No such changes in activity were observed in approximately 50 other neurons subjected to identical magnetic stimuli. The responses of LPe5 were characterized by increases in spiking frequency occurring about 6-16 min after the ambient magnetic field had been rotated to a new position. The response was abolished when the brain had been isolated from the periphery of the animal by severing nerves, a procedure that also transected prominent neurites of LPe5. We hypothesize that LPe5 is one component of a neural circuit mediating detection of the earth's magnetic field or orientation to it.

Animals↗
PubMed1988

Monoclonal antibodies to the molluscan small cardioactive peptide SCPB: immunolabeling of neurons in diverse invertebrates.

We reported a development of murine monoclonal antibodies to a molluscan small cardioactive peptide (SCPB) and their application to immunolabeling of neurons in several molluscan and arthropod species. In vitro stimulations of mouse lymphocytes with SCPB conjugated to a carrier protein yielded exclusively IgM class antibodies; in vivo stimulation resulted in generation of both IgM and IgG classes of antibodies. Monoclonal antibodies of the IgM class labeled identified SCP-containing neuron B11 in the frozen sections of the buccal ganglia of Tritonia diomedia. These antibodies failed to stain any neurons in whole mount preparations. A monoclonal antibody of IgG1 subclass selectively labeled neurons in both frozen sections and whole mount preparations of diverse invertebrate species. Thus, neurons B11, B12, and GE1 and several other neurons of the buccal and gastroesophageal ganglia of T. diomedia bound the antibody, and a similar pattern of immunolabeling was found in the closely related gastropod Tritonia festiva. We also observed SCPB-like immunoreactivity in the central neurons of other nudibranch and pulmonate molluscs and in examples of insect (Acheta domesticus and Tehrmobia domestica) and crustacean (Semibalanus cariosus) classes of the Arthropoda. Our results suggest a specific pattern of distribution of SCPB-like immunoreactivity in the gastropod nervous system and a broad occurrence of SCPB-like antigenicity in the diverse invertebrates.

Animals↗
PubMed1988

Multiple transmitter neurons in Tritonia. I. Biochemical studies.

The buccal ganglia of the marine mollusc Tritonia control a variety of movements associated with feeding, including gut motility. The buccal ganglia and gut contain a class of peptides termed small cardioactive peptides (SCPs). Cobalt backfilling of the nerve which innervates the gut stains several buccal neurons including two pairs of reidentifiable cells, B11 and B12. Both appear white under epiillumination, a characteristic of peptidergic neurons in gastropods. Enzymatic and biochemical analyses of extracts from microdissected B11 cell bodies demonstrate that this neuron contains two species of SCPs. Labeling in organ culture followed by dissection and extraction of cell bodies indicates that these peptides were synthesized in B11. One of these peptides appears to be identical to SCPB, one of two SCPs that have been sequenced. The other SCP present in these neurons is novel. Less extensive analyses of extracts of B12 somata suggest that it also contains the same SCPs. In addition to the peptides, B11 also contains large quantities of acetylcholine (ACh) as determined by a radioenzymatic assay of cell body extracts. B12 does not contain measureable ACh. The concentration of the two peptides and ACh in the B11 cytoplasm is approximately 1 mM. Neuron B11 appears to be an appropriate model system for studying the biochemical and physiological properties of multiple transmitter neurons.

Acetylcholine↗
PubMed1988

Multiple transmitter neurons in Tritonia. II. Control of gut motility.

Two large multiple transmitter neurons are located in each buccal ganglion of Tritonia. One of these neurons (B11) contains large quantities of two neuropeptides and acetylcholine (ACh), whereas the other neuron (B12) appears to contain the same two peptides but no ACh. One of the peptides present in these neurons has recently been sequenced and is termed small cardioactive peptide B (SCPB). Both neurons regulate the motility of the gut. Stimulation of B11 produces a posteriorly directed peristalsis after a short latency. This gut movement may normally accompany swallowing. B11 stimulation also produces an increase in the rate of endogenous contractile activity that is similar to that produced by superfusion of the gut with low concentrations (10(-8) M) of SCPB. Stimulation of B12 produces a vigorous longitudinal contraction of the gut, initiated in the posterior part of the gut and not peristaltic in nature. This movement appears incompatible with swallowing behavior and may be involved in regurgitation.

Acetylcholine↗
PubMed1988

Multiple transmitter neurons in Tritonia. III. Modulation of central pattern generator controlling feeding.

Feeding behavior in the gastropod mollusc Tritonia diomedea is controlled by a central pattern generator (CPG) in the buccal ganglia. The medially located, large dorsal white cells (B11) have been shown to contain two small cardioactive peptides (SCPs). A smaller nearby neuron (B12) also appears to contain the SCPs. B11's have also been shown to contain acetylcholine (ACh), whereas B12's do not. We have shown earlier that intracellular stimulation of B11's drives contractions of the foregut. Here we show that intracellular electrical stimulation of B11's also elicits excitation of neurons B5 and stimulates the patterned motor output of the CPG. We showed earlier that B12's also stimulate contractions in the foregut, but they are in the opposite direction from those elicited by B11. We show here that electrical stimulation of B12's inhibits the output of the CPG. We showed earlier that superfusion of the isolated gut with SCPB enhances peristalsis, and here we report that superfusion of the buccal ganglion with SCPB elicits enhanced coordinated motor output from the CPG. The peptide has two effects on the bursting output of motor neurons. It produces an increase in (1) the rate of bursting and (2) the spike frequency during each burst. On the other hand, we reported earlier that ACh applied directly to isolated foregut inhibits ongoing peristalsis. Here we demonstrate that ACh superfusion of the buccal ganglion also inhibits the CPG output. Our evidence supports the view that in addition to stimulating foregut contractility, B11's modulate the output of the swallowing CPG by releasing a peptide from central terminals. We suggest roles for B11, B12, the SCPs, and ACh in controlling both central and peripheral aspects of feeding behavior.

Acetylcholine↗
PubMed1987

Lunar-modulated geomagnetic orientation by a marine mollusk.

Behavioral experiments indicated that the marine opisthobranch mollusk Tritonia diomedea can derive directional cues from the magnetic field of the earth. The magnetic direction toward which nudibranchs spontaneously oriented in the geomagnetic field showed recurring patterns of variation correlated with lunar phase, suggesting that the behavioral response to magnetism is modulated by a circa-lunar rhythm. The discovery of a magnetic sense in a mollusk with giant, reidentifiable neurons provides a unique opportunity to study the cellular mechanisms underlying magnetic field detection.

Animals↗
PubMed1987

A simple neuronal system characterized by a monoclonal antibody to SCP neuropeptides in embryos and larvae of Tritonia diomedea (Gastropoda, Nudibranchia).

SCP-like antigenicity is first present in Tritonia diomedea in small cells of the cerebral ganglia and a single axon crossing the cerebral commissure of 8-day-old embryos. Other axons and neurons become antigenic as the larva develops. At 4-9 days after larvae hatch from the egg mass, 2 additional pairs of neurons are labeled. Axons extend from one pair to the left cerebral ganglion and from the other to the right. A second labeled axon is present across the cerebral commissure. In metamorphically competent larvae the cerebral and pedal neuropils, as well as two neurons in the buccal ganglia with axon(s?) across the commissure, are antigenic. The change in antigenicity as the larva becomes competent is presumably preparatory for juvenile life. The labeled buccal neurons may be B12, which are known to contain SCPs, extend an axon across the buccal commissure, and function in adult feeding behavior. The two large neurons strongly labeled by rabbit polyclonal antibodies against FMRFamide are clearly different from neurons labeled by monoclonal antibody against SCPs. This result supports the contention that different antigens are labeled by these two immune probes.

Animals↗
PubMed1985

Morphology of two pairs of identified peptidergic neurons in the buccal ganglia of the mollusc Tritonia diomedea.

The morphology of two pairs of identified peptidergic neurons (B11 and B12) located in the buccal ganglia of Tritonia diomedea was described. Both pairs of neurons contained a large quantity of a small cardioactive peptide (SCP) in their somata. One of the pairs (B11), the large dorsal white cells, contained ACh in their somata along with SCP. Both pairs of cells appeared white in live preparations under epi-illumination. Each B11 and B12 was a unipolar neuron and sent its major axonal branch through the ipsilateral gastro-esophageal nerve to the gut. In addition, B12 sent a small branch to the contralateral buccal ganglion. A characteristic feature of both neuron pairs was their vesicular content. Three types of vesicles were observed in B11. Vesicles with electron-lucent core (LCV) and electron-dense core (DCV) were found in the somata. The axon hillock and the beginning of axon contained vesicles with variable electron dense core (VDCV) in addition to LCV and DCV. The ratio of DCV: LCV: VDCV changed from 5:95:0 for the perinuclear cytoplasm to 8:55:37 for the beginning of axon. The average maximum diameters were 97 +/- 23 nm for DCV, 103 +/- 32 nm for LCV and 106 +/- 29 nm for VDCV. B12 somata contained DCV (average maximum diameter 100 +/- 26 nm), LCV (109 +/- 23 nm) and elliptical vesicles with eccentric electron-opaque core (115 +/- 20 nm).

Acetylcholine↗