The External Structure and Distribution of Sensilla in the Medicinal Leech

Abstract The body of Hirudo medicinalis consists of 32 segments. The quinquannulate midbody segments 3–18 bear 14 sensilla on the central (neural) annulus. Elsewhere segments are represented by fewer than five annuli but sensilla are retained on the neural annulus. From neural sensilla protrude S hairs (cilia from uniciliate cells) which are thought to detect water currents. Two categories of multiciliate cell, of unknown function, are also present within neural sensilla; (i) grouped cilia extending beyond the cuticle (G hairs), and (ii) cilia which radiate out beneath the cuticle. Studies of the entire external surface of leech body wall with a scanning electron microscope revealed the presence of large numbers of sensilla on every annulus including the neural annuli. These sensilla lack S hairs. Our results show: (i) annular sensilla have a significantly smaller surface area than neural sensilla (p < 0.001 Mann-Whitney test, 2 tailed), (ii) The position and number of the small sensilla varies from annulus to annulus, segment to segment and individual to individual, (iii) Significantly higher numbers of small sensilla were found where non-neural annuli remain single and have not undergone a further division during development as happens in the quinquannulate segments. The data suggest that small sensilla continue to be added during the adult life of the leech.     

Photosensory input pathways in the medicinal leech

Summary The medicinal leech,Hirudo medicinalis possesses two types of photosensory organs: five bilateral pairs of eyes embedded in two longitudinal rows in the dorsal surface of the head, and seven bilateral pairs of sensilla situated in both the dorsal and the ventral surface of each of the 21 body segments. The photoreceptor cells of each eye or sensillum project their axons centrally via a characteristic cephalic or segmental nerve which carries the photosensory input to the brain or to the segmental ganglion. In response to a pulse of light the photoreceptors produce a train of impulses whose frequency first rises to anearly peak and then declines to asteady state plateau at which it remains until the end of the pulse. The amplitude of the early peak response and the level of the steady state plateau rise linearly with the log of the light pulse intensity, but the dynamic range of the early peak response is much narrower than that of the plateau. Both ocular and sensillar photoreceptors adapt to the intensity of interpulse background illumination; the ocular receptors adapt so completely that their level of background activity is nearly independent of the background light intensity, whereas the ventral sensillar photoreceptors adapt incompletely, so that their background activity rises with the background light intensity. Ocular and sensillar photoreceptors make their maximal response to green light at a wavelength of about 540 nm. They are almost insensitive to red and violet light at both extremes of the visible spectrum. The photosensory response of a single eye is directionally selective, whereas that of a single sensillum has much less directional selectivity. Several higher order sensory neurons were identified in the segmental ganglion that receive photosensory input from the sensilla. One of these neurons has the sensillum in the ipsilateral dorso-medial body wall of the same segment as its receptive field and another neuron the bilateral set of ventral sensilla in the body wall of the next posterior segment.We are indebted to Frank S. Werblin for valuable advice and discussions. We thank Kenneth L. Carlock for designing and constructing much of the special electronic equipment used in this study. We also thank Alexander Petruncola for his helpful suggestions regarding the computational analysis of the experimental results and for writing the computer programs used in the processing of the data.This research was supported by Grant No. GB 31933X from the National Science Foundation, and NIH research grant No. GM 17866 and Training Grant No. GM 00829 from the Institute for General Medical Sciences.     

A proposal to regard the former family Naididae as a subfamily within Tubificidae (Annelida, Clitellata)

A new species of Placobdelloides is described from crocodiles and river turtles in the Singapore Zoological Gardens. Placobdelloides stellapapillosa is three annulate, has one pair of eyes on somite I or II, six pairs of testisacs, two annuli between the gonopores, one post anal annulus, seven pairs of lobed crop caeca and 12–14 unique star-shaped papillae on the dorsal surface of each annulus. Star-shaped papillae on annulus a2 are typically larger and more pronounced than on annuli a1 and a3. Additional minute cone-shaped papillae may occur between the larger star-shaped papillae or may replace these papillae on annuli a1 and a3. Eggs and young (100–200) are attached by their posterior suckers directly to the ventral surface of the parent.     

Gangliogenesis in leech: morphogenetic processes leading to segmentation in the central nervous system

 Using intracellular lineage tracers to study the main neurogenic lineage (N lineage) of the glossiphoniid leech embryo, we have characterized events leading from continuous columns of segmental founder cells (nf and ns primary blast cells) to discrete, segmentally iterated ganglia. The separation between prospective ganglia was first evident as a fissure between the posterior boundary of nf- and the anterior boundary of ns-derived progeny. We also identified the sublineages of nf-derived cells that contribute parallel stripes of cells to each segment. These stripes of cells project ventrolaterally from the dorsolateral margin of each nascent ganglion to the ventral body wall. The position and orientation of the stripes suggests that they play a role in forming the posterior segmental nerve; they are not coincident with the ganglionic boundary, and they form well after the separation of ganglionic primordia. Previous work has shown that cells in the anterior stripe express the leech engrailed-class gene. Thus, in contrast to the role of cells expressing engrailed in Drosophila, the stripes of N-derived cells expressing an engrailed-class gene in leech do not seem to play a direct role in segmentation or segment polarity. Received: 10 October 1997 / Accepted: 12 December 1997     

The nervous system of the tube-worm Chaetopterus variopedatus (Polychaeta)

Silver impregnation of serial histological sections of the tubeworm Chaetopterus variopedatus revealed the presence of a subepidermal nervous system. The anterior nervous system is delimited by the first 11 segments and comprises (1) two dorsolateral cerebral ganglia and lateral instead of ventral nerve cords which are widely separated and thus connected by unusually long commissures, (2) a pharyngeal ganglion in the fourth segment which is connected to the cerebral ganglia by pharyngeal nerves and constitutes along with the pharyngeal plexus a stomatogastric or enteric nervous system, and (3) small, presumably segmental ganglionic swellings along the lateral nerve cords from which emerge commissures and parapodial nerves. No subesophageal ganglion or periesophageal connective could be identified. The lateral nerve cords converge toward the midline in the 12th segment to form the posterior nervous system comprising a pair of ventromedian nerve cords with their repetitive segmental ganglia from which emerge numerous short commissures and three segmental nerves coursing toward the dorsal and ventral regions of parapods and toward the neuropod. Light and electron microscopic investigations of cerebral and segmental ganglia showed an arrangement of inner neuropile and of unipolar neuron somata at the periphery. The neuropile comprises numerous neurites ranging in diameter from 0.5 to 10 μm and making polarized or symmetrical synaptic junctions with each other. The pharyngeal ganglion consists of a similar neuropile and of a large mass of cell bodies which is traversed by an elaborate network of sinuses and harbors three types of neurosecretory cells in addition to the conventional neuron somata. These findings are interpreted in the framework of the highly specialized morphological features and habits of Chaetopterus, and the welldeveloped stomatogastric system is considered to be related to control of the feeding activities.     

Homonomies within the ventral muscle system and the associated motoneurons in the locust,Schistocerca gregaria (Insecta,Caelifera)

To understand the segmental reiteration of an insect, the serially arranged neuromuscular system of the locust, Schistocerca gregaria, is studied. The ventral muscle system is chosen and its motoneuronal supply is described in the thoracic and pregenital segments. In general, repetitively arranged, similar sets of motoneurons (MNs) supply the ventral muscles of these segments. Common criteria of both topology of muscles and neural features (nerve branches and motoneuronal supply) suggest possible homonomies of the ventral longitudinal muscles and ventral diaphragm of the thoracic and abdominal system. Based on a segment-by-segment analysis, muscle topology and motor supply match, in most instances. There are, however, cases where such a parallelism is missing. In a particular cases the supply of apparently homonomous muscles shifts from one set of MNs to another. In another case, putatively equivalent MNs of different ganglia supply morphologically different muscle structures in the adult animal. Therefore, it becomes apparent that muscles and their supplying MNs are, in principle, independent elements which might be subjected autonomously to ontogenetic processes. As a consequence, in the search for the basic segmental Bauplan depending on homonomous structures, muscles and MNs have to be regarded as separate entities.Abbreviations A1–6 abdominal ganglion (or neuromere A1–3) - AS1–6 abdominal segment 1–6 - DUM doisal unpaired median - M muscle (number) - MN motoneuron - N nerve (number) - PMN paramedian nerve - T1–3 pro-, meso-, metathoracic ganglion - TS1–3 pro-, meso-, metathoracic segment - VD ventral diaphragm - VM ventral muscle     

Molecular re-assessment of some phylogenetic,taxonomic and biogeographic relationships between the leech genera Dina and Trocheta (Hirudinea: Erpobdellidae)

The three most abundant and species-rich genera of erpobdellid leeches – Erpobdella, Dina and Trocheta – have traditionally been distinguished by their annulation pattern. Erpobdella has five unsubdivided annuli per somite, in Dina the last annulus is widened and subdivided once, and in Trocheta, the last and often also the first annulus is further subdivided. The last two genera are often referred to as the subfamily Trochetinae. The presented molecular phylogenetic analysis, based on mitochondrial 12S rDNA sequences and nuclear ITS2 sequences, has revealed a sister relationship between Trocheta and Erpobdella rather than between Trocheta and Dina. Furthermore, the annulation pattern has proved to be inappropriate for the diagnosis of Dina and Trocheta. The taxon Trocheta bykowskii krasensehas been classified on the basis of its Trocheta-like annulation; however, according to the molecular phylogeny, it belongs to the Dina clade. A pair of diagnostic PCR primers were developed to identify unambiguously individuals with intermediate annulation. In summary, (1) the traditional genus diagnosis of Dina and Trocheta is no longer tenable, and the genera are not always morphologically distinguishable by traditional characters; (2) T. b. krasense Sket, 1968, should be re-classified as Dina krasensis; (3) the subfamily Trochetinae should be annulled because it does not represent a monophyletic assemblage.     

Multisegmental cobalt filling of the dorsal giant fibers in the nervous system of the earthworm,Lumbricus terrestris

Summary The anatomical organization of the two dorsal giant fiber systems of the earthworm Lumbricus terrestris is demonstrated in whole mounts and serial-section reconstructions based on backfillings of the ventral nerve cord with cobalt chloride. Both the medial and lateral fiber systems can be labeled selectively over more than ten body segments. They show a characteristic segmental pattern of collaterals with some modification in tail segments and of dorsal plasma protrusions in the unpaired medial giant fiber presumably representing openings in the myelin sheath. We found no multisegmental cobalt transport in other large neurons of the nerve cord. Cobalt passes through the segmentai septa between consecutive axonal elements of the metameric giant fibers and presumably also through commissural contacts between specific collaterals of the lateral giant fibers. Since these sites of contact are known to represent electrical synapses, cobalt coupling may, in L. terrestris, correlate with functional electrotonic coupling.Abbreviations CL collateral of lateral giant fiber - CM collateral of medial giant fiber - GIN giant interneuron - LGF lateral giant fiber - MGF medial giant fiber - SN segmental nerve     

Embryonic cell lineages in the nervous system of the Glossiphoniid leech Helobdella triserialis

The lines of descent of cells of the nervous system of the leech Helobdella triserialis have been ascertained by injection of horseradish peroxidase (HRP) as a tracer into identified cells of early embryos. Such experiments show that the nervous system of the leech has several discrete embryological origins. Some of the neurons on one side of each of the segmental ganglia derive from a single cell, the ipsilateral N ectoteloblast. Other neurons derive from a different precursor cell, the ipsilateral OPQ cell that gives rise to the O, P, and Q ectoteloblasts. The positions within the ganglion of neuronal populations derived from each of these sources are relatively invariant from segment to segment and from specimen to specimen. Other nerve cord cells derive from the mesoteloblast M; of these four per segment appear to be the precursors of the muscle cells of the connective. The A, B, or C macromeres contribute cells to the supraesophageal ganglion. In preparations in which an N ectoteloblast was injected with HRP after production of its bandlet of n stem cells had begun, the boundary between unstained (rostral) and stained (caudal) tissues can fall within a ganglion or between ganglia. This suggests that each hemiganglion contains the descendants of more than one, and probably two, n stem cells.     

Diplosegmentation in the pill millipede Glomeris marginata is the result of dorsal fusion

All trunk segments in the pill millipede Glomeris marginata (Myriapoda: Diplopoda) are initially patterned genetically, (as visualized by the embryonic expression pattern of the even‐skipped gene) and formed morphologically, (as visualized by 4‐6‐diamidin‐2‐phenylindol stained embryos) in a single segmental period. In addition, formation of every nascent trunk segment concerns ventral as well as dorsal segmental units. Only after the formation of the nascent posterior trunk segments, the dorsal segmental units of two adjacent segments fuse to form a single dorsal segmental unit that subsequently covers two ventral leg‐bearing segmental units. The formation of a diplosegmental unit, or in short a diplosegment, is thus the result of dorsal fusion of embryonic tissue and not the result of any splitting‐process or fusion of dorsal tergites. The new data also argue against heterochrony as a primary causative factor for the formation of the diplosegments during the formation of dorsal versus ventral segmental units. Furthermore, no evidence was found supporting the hypothesis that anterior trunk segments in diplopods represent degenerate diplosegments. Two possible scenarios arise from the ontogenetic data presented here, whether this represents an ancestral feature of the diplopods, or alternatively if they represent an isolated case only found in Glomeris (and close relatives). If the former is the case, my work may provide an impressive example of Haeckel's recapitulation theory.     

Patterns of serotonin-immunoreactive neurons in the central nervous system of the earthworm Lumbricus terrestris L.

Summary The distribution patterns of serotonin-immunoreactive somata in the cerebral and subpharyngeal ganglion, and in the head and tail ganglia of the nerve cord of Lumbricus terrestris are described from whole-mount preparations. A small number of serotonin-immunoreactive neurons occurs in the cerebral ganglion, in contrast to the large population of serotonin-immunoreactive neurons that exists in all parts of the ventral nerve cord. From the arrangement of serotonin-immunoreactive somata in the subpharyngeal ganglion, we suggest that this ganglion arises from the fusion of two primordial ganglia. In head and tail ganglia, the distribution of serotonin-immunoreactive somata resembles that in midbody segments. Segmental variations in the pattern and number of serotonin-immunoreactive somata in the different body regions are discussed on the background of known developmental mechanisms that result in metameric neuronal populations in annelids and arthropods.Abbreviations CG1, CG2 cerebral soma group 1, 2 - CNS central nervous system - GINs giant interneurons - 5-HT 5-hydroxytryptamine, serotonin - 5-HTi 5-HT-immunoreactive - N side nerve - SG19 subpharyngeal soma group 1–9 - SN segmental nerve     

<Emphasis Type="Italic">Hau-Pax6A</Emphasis> expression in the central nervous system of the leech embryo

The leech Helobdella sp. (Austin) has two genes of the Pax6 subfamily, one of which is characterized in detail. Hau-Pax6A was expressed during embryonic development in a pattern similar to other bilaterian animals. RNA was detected in cellular precursors of the central nervous system (CNS) and in peripheral cells including a population associated with the developing eye. The CNS of the mature leech is a ventral nerve cord composed of segmental ganglia, and embryonic Hau-Pax6A expression was primarily localized to the N teloblast lineage that generates the majority of ganglionic neurons. Expression began when the ganglion primordia were four cells in length and was initially restricted to a single cell, n_s.a, whose descendants will form the ganglion’s anterior edge. At later stages, the Hau-Pax6A expression pattern expanded to include additional CNS precursors, including some descendants of the O teloblast. Expression persisted through the early stages of ganglion morphogenesis but disappeared from the segmented body trunk at the time of neuronal differentiation. The timing and iterated pattern of Hau-Pax6A expression in the leech embryo suggests that this gene may play a role in the segmental patterning of CNS morphogenesis.     

Control of leech swimming activity by the cephalic ganglia

We investigated the role played by the cephalic nervous system in the control of swimming activity in the leech, Hirudo medicinalis, by comparing swimming activity in isolated leech nerve cords that included the head ganglia (supra- and subesophageal ganglia) with swimming activity in nerve cords from which these ganglia were removed. We found that the presence of these cephalic ganglia had an inhibitory influence on the reliability with which stimulation of peripheral (DP) nerves and intracellular stimulation of swim-initiating neurons initiated and maintained swimming activity. In addition, swimming activity recorded from both oscillator and motor neurons in preparations that included head ganglia frequently exhibited irregular bursting patterns consisting of missed, weak, or sustained bursts. Removal of the two head ganglia as well as the first segmental ganglion eliminated this irregular activity pattern. We also identified a pair of rhythmically active interneurons, SRN1, in the subesophageal ganglion that, when depolarized, could reset the swimming rhythm. Thus the cephalic ganglia and first segmental ganglion of the leech nerve cord are capable of exerting a tonic inhibitory influence as well as a modulatory effect on swimming activity in the segmental nerve cord.     

Similarities and differences in the structure of segmentally homologous neurons that control the hearts in the leech,Hirudo medicinalis

Summary The neural circuit that controls the hearts in the leech comprises an ensemble of synaptically interconnected cardiac motor neurons (HE cells) and cardiac interneurons (HN cells). Both the HE cells and the HN cells constitute segmentally homologous sets. We have investigated the structure of these neurons by iontophoretic injection of Lucifer Yellow dye.Bilateral pairs of HE cells have been identified in segmental ganglia 3–19 of the nerve cord. Their structure was found to be nearly identical from ganglion to ganglion and from animal to animal.Bilateral pairs of HN cells have been identified in segmental ganglia 1–7 of the nerve cord. Their dendritic structure was found to vary from ganglion to ganglion. These segmental differences among HN cells were observed consistently from animal to animal. Some of the segmental differences in HN cell structure correlate with previously described physiological differences.     

Anteroposterior patterning is required within segments for somite boundary formation in developing zebrafish

Somite formation involves the establishment of a segmental prepattern in the presomitic mesoderm, anteroposterior patterning of each segmental primordium and formation of boundaries between adjacent segments. How these events are co-ordinated remains uncertain. In this study, analysis of expression of zebrafish mesp-a reveals that each segment acquires anteroposterior regionalisation when located in the anterior presomitic mesoderm. Thus anteroposterior patterning is occurring after the establishment of a segmental prepattern in the paraxial mesoderm and prior to somite boundary formation. Zebrafish fss(-), bea(-), des(-) and aei(-) embryos all fail to form somites, yet we demonstrate that a segmental prepattern is established in the presomitic mesoderm of all these mutants and hox gene expression shows that overall anteroposterior patterning of the mesoderm is also normal. However, analysis of various molecular markers reveals that anteroposterior regionalisation within each segment is disturbed in the mutants. In fss(-), there is a loss of anterior segment markers, such that all segments appear posteriorized, whereas in bea(-), des(-) and aei(-), anterior and posterior markers are expressed throughout each segment. Since somite formation is disrupted in these mutants, correct anteroposterior patterning within segments may be a prerequisite for somite boundary formation. In support of this hypothesis, we show that it is possible to rescue boundary formation in fss(-) through the ectopic expression of EphA4, an anterior segment marker, in the paraxial mesoderm. These observations indicate that a key consequence of the anteroposterior regionalisation of segments may be the induction of Eph and ephrin expression at segment interfaces and that Eph/ephrin signalling subsequently contributes to the formation of somite boundaries.     

The caudal ganglion of the leech,with particular reference to homologues of segmental touch receptors

The caudal ganglion of the leech, which provides sensory and motor innervation to the posterior sucker, represents the fusion of seven embryonic segmental ganglia. Although fused, each of the seven contributing ganglia (“subganglia”) of the caudal ganglion can be distinguished morphologically and functionally. The roots from each subganglion carry the axons of mechanoreceptors homologous to “touch” cells found in the segmental ganglia and the subesophageal compound ganglion. The receptive fields supplied by the touch cells of the caudal ganglion are uniquely arranged and reveal the modified segmentation of the circular posterior sucker. Extensive overlap of sensory innervation occurs between adjacent segments of the sucker, beyond the overlap characteristic of the homologous cells of body segments. It thus appears that the touch receptors of the caudal ganglion are less restricted than receptors of the segmental ganglia with regard to their territories of innervation. The caudal ganglion has additional unique properties that establish it as a distinct integrative center of the leech CNS.     

The contribution made by cells from a single somite to tissues within a body segment and assessment of their integration with similar cells from adjacent segments

Somites represent the first visual evidence of segmentation in the developing vertebrate embryo and it is becoming clear that this segmental pattern of the somites is used in the initial stages of development of other segmented systems such as the peripheral nervous system. However, it is not known whether the somites continue to contribute to the maintenance of the segmental pattern after the dispersal of the somitic cells. In particular, the extent to which cells from a single somite contribute to all of the tissues of a single body segment and the extent to which they mix with cells from adjacent segments during their migration is not known. In this study, we have replaced single somites in the future cervical region of 2-day-old chick embryos with equivalent, similarly staged quail somites. The chimerae were then allowed to develop for a further 6 days when they were killed. The cervical region was dissected and serially sectioned. The sections were stained with the Feulgen reaction for DNA to differentiate between the chick and quail cells. The results showed that the cells from a single somite remained as a clearly delimited group throughout their migration. Furthermore, the sclerotome, dermatome and myotome portions from the single somites could always be recognised as being separate from similar cells from other somites. The somitic cells formed all of the tissues within a body segment excluding the epidermis, notochord and neural tissue. There was very little mixing of the somitic cells between adjacent segments. The segmental pattern of the somites is therefore maintained during the migration of the somitic cells and this might be fundamental to a mechanism whereby the segmentation of structures, such as the peripheral nervous system, is also maintained during development.     

Paradox segmentation along inter- and intrasomitic borderlines is followed by dysmorphology of the axial skeleton in the open brain (opb) mouse mutant

In open brain (opb) mutant embryos, developmental defects of the trunk spinal cord were spatially correlated with severe defects of the epaxial somite derivatives including sclerotomes, whereas hypaxial somite derivatives are much less affected. Later in development, the neural arches (epaxial sclerotome derivatives) formed but were severely disorganized, and also the distal ribs (hypaxial sclerotome derivatives) were malformed. Adjacent neural arches and vertebral bodies were often fused where joints should have formed suggesting defects of the intrasomitic borderlines. Moreover, neural arches frequently and ribs sometimes were split into halves at distinct levels along the dorso-ventral body axis. This suggests that ‘resegmentation’ of sclerotomes across the somite borders did not completely occur. These prominent skeletal defects were preceded by reduced expression of Pax1 along the intrasomitic borderlines, and incomplete maintenance of somite borders between central sclerotome moieties. The defects of the axial skeleton were accompanied by segmentation defects of the myotomes which were split distally, and also partly fused from adjacent segments across somite borders. The segmentation defects observed suggest that in opb mutants both segmental borderlines, the somite borders and the intrasomitic borderlines (fissures), were affected and behaved paradoxically. Dev. Genet. 22:359–373, 1998. © 1998 Wiley-Liss, Inc.     

Segmental diversification of an identified leech neuron correlates with the segmental domain in which it expresses lox2, a member of the hox gene family

The cellular colocalization of LOX2 protein and small cardioactive peptide (SCP)-like immunoreactivity was studied in the nerve cord of the glossiphoniid leech Helobdella triserialis. Of the six neurons that express SCP in the midbody segments 7 to 17, only one, the MPS neuron, expresses LOX2 protein. The medial paired SCP (MPS) neurons are segmentally repeated and can be divided into three contiguous segmental domains according to cell body size and the timing and level of SCP expression. MPS neurons located in the anterior and middle segmental domains express LOX2 protein. In the middle domain, large MPS neurons begin to accumulate SCP shortly after the end of embryonic development, whereas in the anterior domain the MPS neurons are smaller and begin to express SCP at a later stage. In the posterior domain the MPS neurons exhibit a third phenotype—they have large cell bodies, express low levels of SCP starting from the midjuvenile stage, and do not show detectable LOX2 expression. Lineage tracer injections showed that the MPS neurons arise from a stereotyped cell lineage and are descended from the O teloblast stem cell. In midbody ganglia 2 to 6 and 18 to 21, there are lineally homologous neurons that do not express either LOX2 protein or SCP. Thus, the boundaries of LOX2 expression coincide precisely with two of the segmental boundaries of MPS differentiation, suggesting that expression of Lox2 at the level of this single identified neuron governs some, but not all, aspects of the neuron's segmental diversification. © 1996 John Wiley & Sons, Inc.