1 Overview
The alimentary system, one of the most complex portions of the
nematode anatomy, is composed of a large variety of tissues and cell
types (White, 1988). Direct intercellular
connections between the alimentary tissues and the rest of the body are
minimal. Topologically, this system forms a separate epithelial tube
running inside the cylindrical body wall, separated from it by the
pseudocoelomic space, and placed parallel to the gonad. At the
anteriormost end, the pharyngeal epithelium connects to the arcade
cells of the lips (See Interfacial Epithelial Cells).
The posteriormost region of the alimentary tract, the rectal
epithelium and anus, is surrounded by the tail hypodermis and the
dorsorectal ganglion. One pair of somatic neurons (RIPL/RIPR) penetrates the pharyngeal basal lamina to make gap junctions with a pair of pharyngeal neurons (I1L/R).
Otherwise the only connection that spans the two systems (somatic vs.
enteric) are the four specialized enteric muscle cells that act on the
intestine and rectal valve while being driven by the somatic motor
neurons, AVL and DVB.
The alimentary system is divided into the foregut (stomodeum; buccal
cavity and the pharynx), the midgut (intestine), and the hindgut
(proctodeum; rectum and anus in hermaphrodites and cloaca in males) and
contains a total of 127 cells (AlimFIG 1). The stomodeum and proctodeum are lined with cuticle, which is shed along with body cuticle during molts (See Cuticle) (Bird and Bird, 1991).
The stomodeum and proctodeum are also regions into which enteric
glands open; pharyngeal glands open to the stomodeum and rectal glands
open to the proctodeum. Ingested material flows through the digestive
tract by the muscular pumping and peristalsis of the pharynx at the
anterior end, and the waste material is discarded through the opening of
the anus at the posterior end by the action of the enteric muscles.
The intestine itself is devoid of any muscular structure in C. elegans, although its rear portion can be contracted by the stomatointestinal (SI) muscles (see Intestine).
During defecation, the body wall muscles also contribute to the
control of internal pressure and concentration of the gut contents
before the expulsion of the waste material (see Rectum and Anus).
Developmentally, the intestine is endodermal in origin, whereas the
stomodeum and proctodeum have a mixed lineage from ectodermal and
mesodermal origins (Bird and Bird, 1991).

AlimFIG 1: The alimentary system in C. elegans. A. Schematic drawing of the alimentary system of C. elegans. B. The C. elegans
alimentary system is derived polyclonally from the EMS (posterior
pharynx is derived mainly from MS and intestine from E) and AB (anterior
pharynx is derived mainly from ABa and rectum from ABp) lineages.
(Based on Fukushige et al., 1996.) C. Lineage
tree and cell divisions that give rise to the pharynx and the
intestine. Intestinal cells are derived from a single blast cell E,
whereas the pharyngeal cells are derived from both the AB and MS blast
cells. E daughters are clonal, whereas AB and MS daughters have mixed
cell fates. (Green) Pharyngeal lineages; (pink)
intestinal lineages. The bar on the left indicates time after
fertilization, stages of development and cell migrations during
embryonic development at 20°C.
The alimentary system is described in different sections by its
individual organs along the length of the body, from anterior to
posterior (see Pharynx, Intestine and Rectum and Anus sections and also Pharynx Atlas).
The tissues that connect to the pharyngeal epithelium and are more
anterior to the pharyngeal epithelium within the lips (hyp1, hyp2, hyp3,
the lip sensilla, and the arcade cells) are described in the Epithelial System - Hypodermis. |
2 References
Bird, A. F. and Bird, J. 1991. The structure of nematodes. Academic Press, California.
White, J. 1988. The Anatomy. In The nematode C. elegans (ed. W. B. Wood). Chapter 4. pp 81-122. Cold Spring Harbor Laboratory Press, New York. Abstract
Fukushige, T., Schroeder, D.F., Allen,
F.L., Goszczynski, B. and McGhee, J.D. 1996. Modulation of gene
expression in the embryonic digestive tract of C. elegans. Dev. Biol. 178: 276-288. Abstract
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