The nerve ring of the nematode Caenorhabditis elegans: Sensory input and motor output

Abstract

The general organization and structure of the nerve ring, the main mass of central nervous system neuropil, in the small soil nematode Caenorhabditis elegans is described. The nerve ring receives sensory input from the anterior tip of the animal by means of six nerve bundles, all nerve fibers of which have centrally located cell bodies. The anterior sensory structures are classically divided into two types, papillary and amphidial, and are assumed responsible for mechano-and chemoreception, respectively. Papillary fibers enter directly into the nerve ring, whereas amphidial fibers enter the ventral ganglion, a posterior extension of the nerve ring, in a circuitous manner which is not discussed in detail. Of those papillary fibers which project into the nerve ring neuropil, 22 end in easily characterized sensory structures whereas 14 terminate distally near sensory organs but have no function which can be deduced on the basis of comparative morphology. After entering the ring the fibers maintain their identity and do not anastamose with one another. Cell bodies of each papillary sensory neuron have been mapped around the nerve ring. The cephalic musculature is shown to consist of 32 muscle cells which form four longitudinal submedial groups of eight muscles each. Innervation of this musculature occurs wholly within the CNS by means of processes of the muscle cells which are sent centrally. The anterior 16 cephalic muscle cells are innervated by the ring only, in well delimited regions termed muscle plates. The posterior 16 are dually innervated by means of processes sent both to the nerve ring plates and to their nearest medial longtitudinal nerve cord. The nerve ring neuropil is characterized as having fibers containing one of four morphologically distinct vesicle types. Gap junction contacts are observed within the main neuropil involving one of these fiber types and within the muscle plate regions among muscle processes, which do not contain vesicles. An evolutionarily primitive sensory-motor synapse within the nerve ring is described from an identified sensory neuron onto an identified cephalic muscle cell process. Comparisons are made with the nervous system of Ascaris lumbricoides, the only other nematode to be extensively studied, to illustrate the conservativeness of the nemic nervous system.

The Molecular Identities of the Caenorhabditis elegans Intraflagellar Transport Genes dyf-6, daf-10 and osm-1

“…Those in the region of the inner labial neurons may correspond to the IL2 neurons, which, like the phasmid and dye-filling amphid neurons, are ciliated and are exposed to the environment (Ward et al 1975;Ware et al 1975). The pattern of expression of DYF-6TGFP appears to be a subset of that seen with OSM-6TGFP, which is expressed in nearly all (56 of 60) of the ciliated neurons of C. elegans (Collet et al 1998).…”

Mutation of the MAP kinase DYF-5 affects docking and undocking of kinesin-2 motors and reduces their speed in the cilia of Caenorhabditis elegans

“…The microtubular axoneme in the middle segment consisted of a ring of nine doublet microtubules and up to six singlet microtubules ( Fig. 3D) (7,32,33). In the tip of the cilium the nine microtubules were all singlets ( Fig.…”

“…In the tip of the cilium the nine microtubules were all singlets ( Fig. 3D) (7,32,33). In the dyf-5(lf) mutant, the morphology of the cilia was severely affected.…”

Electrical activity and behavior in the pharynx of caenorhabditis elegans

“…Such a dual function may provide a single-cell reflex loop: M3 may sense contraction of the pharynx and then command its relaxation. In addition to M3, several other pharyngeal neuron types (Albertson and Thomson, 1976) and at least one extrapharyngeal neuron type (Ward et al, 1975;Ware et al, 1975) have been proposed to have both sensory and motor roles based on anatomical data, so it is likely that other C.elegans neurons have dual physiological functions as proposed.…”