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The cellular organisation of the olfactory rosettes of Etroplus suratensis was studied by light and scanning electron microscopy. The oval shaped olfactory rosette of the fish consists of 12 lamellae radiating from a central raphe. The olfactory lamellae are comprised of restricted areas of sensory epithelium and broad areas of non-sensory epithelium in the apical, middle, and basal regions. The sensory epithelium contains three types of receptor cells: microvillus, ciliated, and rod cells, as well as labyrinth cells and supporting cells. The non-sensory epithelium consists of stratified epithelial and mucous cells. The transitional region between the sensory and non-sensory epithelium consists of ciliated receptor cells, mucous cells, and stratified epithelial cells. The different cells on the olfactory epithelium were discussed regarding the functional significance of the fish concerned. (Folia Morphol 2010; 69, 3: 154–159)
The unhatched, newly hatched and free-swimming coracidia of Bothriocephalus clavibothrium Ariola, 1899 an intestinal parasite of the teleostean fish Arnoglossus laterna (Walbaum, 1792) (Pleuronectidae) from the Mediterranean Sea near Séte, France were examined by means of transmission electron microscopy (TEM) and cytochemistry methods. Each unhatched and hatched coracidium of B. clavibothrium is composed of a hexacanth larva, oncosphere, about 28 µm in diameter, surrounded by a 5-7 µm thick ciliated envelope containing about 16 mesomere nuclei and a large amount of nutritive reserves (α- and ß-glycogen and lipids). Several cell types were distinguished within the oncosphere: (1) binucleated subtegumental cell; (2) two flame cells; (3) binucleated penetration gland; (4) two nerve cells; (5) about 100 intermediate, somatic cells which represent perikarya of both somatic and hook musculature; (6) about 50 small embryonic cells, some of them with pycnotic nuclei containing very dense chromatin and showing evident signs of regression and degeneration; and (7) about 10 to 12 germinative cells with prominent nucleoli in large lobate nuclei, surrounded by a thin layer of compact, granular cytoplasm rich in RNA. Apoptosis of numerous micromeres and of outer-envelope and ciliated-envelope material was frequently observed. The total number of oncospheral cells is about 160, the highest number reported from various orders and families of cestodes. This number, along with our own data from different cestode orders and families, supports our hypothesis that the progressive reduction in oncosphere cell numbers is correlated with a simplification of the infective larval stages and is a general trend in cestode evolution. This correlation represents an interesting ontogenic adaptation to the parasitic way of life.
The cellular organisation of the infective eggs of I. madagascariensis has been reconstructed at light (LM) and electron microscopy (EM) level from serial semithin (LM) and ultrathin sections (EM). The oncospheres are surrounded by parenchymatic capsules. The total number of oncospheral cells' is about 44 (50 nuclei). Among them, five major cell types have been distinguished. These consisted of: (1) a six-nucleate, U-shaped penetration gland; (2) a bi-nucleate medullary centre (= sunken perikaryon of oncospheral tegument); (3) two nerve cells of neurosecretory type; (4) about 30 somatic cells (= myocytons of hook and somatic musculature); and (5) about 12 germinative cells (two groups of 6 cells), localised in the posterior pole of the hexacanth. The functional ultrastructure of hook-muscle system and penetration gland and their role in host tissue penetration are discussed.
The cellular organisation of the oncospheres of S. stefanskii has been examined by means of light and transmission electron microscopy. The reconstruction of hexacanth larvae was based on serial semithin sections and its results have been correlated with partial reconstruction from ultrathin sections. The surface of the oncospheres was covered by a thin layer of oncospheral tegument. Five major cell types have been distinguished in mature oncospheres of S. stefanskii: (1) about 10 germinative cells, situated in the posterior pole of the oncosphere; (2) about 36 somatic cells (= myocytons of somatic and hook muscles); (3) a bi-nucleate medullary centre representing a perikaryon of oncospheral tegument; (4) a bi-nucleate, U-shaped penetration gland and (5) two nerve cells containing characteristic dense-core vesicles. The total number of cells in mature oncospheres was thus about 50, while the number of nuclei was about 52. The hook-muscle system of oncospheres, composed of peripheral and hook muscles, is similar to that described in other cyclophyllideans. The oncospheral hooks were formed in specialised hook-forming cells or oncoblasts. The oncoblasts are retained in mature oncospheres only as a thin layer of anucleated cytoplasm around the hook handle region, which seems to be a common feature for the mammalian hymenolepidids. The data on the oncospheral cell types and their number are in agreement with formerly proposed hypothesis (Swiderski 1972, 1983), assuming that the progressive reduction in number of oncospheral cells is one of the characteristic features in cestode evolution.
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