Fine structural analysis of the epithelial cells in the hepatopancreas of Palaemonetes argentinus (Crustacea, Decapoda, Caridea) in intermoult

The aim of this study is to describe the ultrastructure of the hepatopancreas of P argentinus in intermoult. P argentinus hepatopancreas was studied using standard TEM techniques. Each tubule consists of four cellular types: E (embryonic), F (fibrillar), R (resorptive) and B (blister like). E-cells have embryonic features and some of them were found in mitosis. F, R and B cells possess an apical brush border. F-cells have a central or basal nucleus, a conspicuous RER, and dilated Golgi cisternae. R cells show a polar organization of organelles in three areas: apical, with numerous mitochondria and sER tubules, a central are a with the nucleus and RER, and a basal area containing a sER-like tubule system and mitochondria. B-cells were observed at different stages of their life cycle. In an early differentiation stage they comprise an apical endocytotic complex and Golgi vesicles. The fusion of endocytotic and Golgi vesicles originates subapical vacuoles. During maturation, a big central vacuole is formed by coalescence of subapical vacuoles. The central vacuole is eliminated by holocrine secretion. The ultrastructure suggests that F-cells synthesize proteins, R-cells storage nutrients and B-cells have a secretory or excretory function, and confirms the independent origin of F, B and R cells from the embryonic cells

Changes in the hepatopancreas histology of Palaemonetes argentinus (Crustacea, Caridea) during moult

The present work describes the histological changes in the hepatopancreas of Palaemonetes argentinus during the moulting cycle. The hepatopancreas of individuals at different moult stages were dissected and studied using histological techniques. The hepatopancreas in intermoult presents four typical cell types (E, F, R and B) and follows the general plan of the rest of decapods. During early premoult (D1), there is an important secretory activity and many R-cells have several subapical vacuoles and are highly columnar. In early postmoult (A), B-cells are confined to the proximal zone of the tubules. Some of the tubules show a folded basal lamina in late premoult and postmoult. Degenerative desquamation occurs at the proximal zone of the tubules in all the stages, this zone being replenished by mitosis of E cells. Mucopolysaccharides and glycogen reserves are more abundant in premoult than in the rest of the cycle. Cellular height increased in premoult and decreased towards the intermoult, stage of more stability. R-cells are the most abundant, and F-cells do not change significantly through the cycle. The observations suggest that the hepatopancreas of P. argentinus undergoes a significant dynamic and cellular turn over rate in relation to moult.

Histology of the hepatopancreas of the freshwater prawn Palaemonetes argentinus (Crustacea, Caridea)

The aim of this study is to describe the histological structure of the hepatopancreas of P. argentinus in intermoult stage in order to provide a baseline for future analysis of its modifications as indicator of environmental stress. Adults at sexual rest of both sexes were collected from Sotelo stream, tributary of Mar Chiquita lagoon, Argentina (38 degrees S 55 degrees W). P. argentinus hepatopancreas was studied by using histological techniques. The hepatopancreas is a bilaterally bilobed brown-yellowish organ. The structure is formed by a mass of blind tubules, with scarce intertubular space. Each tubule consists of a cylindrical epithelial layer surrounded by a basal lamina and myoepithelial cells. Four cellular types were recognized which represent E (embryonic), F (fibrillar), R (resorptive) and B (blisterlike) cells of other decapods. E-cells were found in mitosis and some F-cells had signs of cellular death. B-cells were observed in different phases of holocrine secretion and some groups of desquamated cells appeared at medial and proximal zones, revealing an important cellular turnover rate. According to these observations F, R and B cells are differentiated independently from E-cells.