In vitro effect of rabbit anti sea star lymphocyte serum on axial organ cells

The axial organ (AO-cells) of the sea star Asterias rubens is a primitive immune organ. The total population was fractionated or not into two populations: adherent (B-like) and non adherent (T-like) to nylon wool. Rabbit anti sea star lymphocyte serum induces the proliferation of axial organ cells. The T-like antiserum stimulates the T-like cells exclusively; the whole axial organ cell antiserum only stimulates the whole axial organ cell population.     

Homologous antigen for T cell receptor in axial organ cells from the asterid Asterias rubens.

The axial organ (A.O. cells) of the sea star Asterias rubens is a primitive immune organ. The total population was fractionated into two populations: adherent (B-like) and non-adherent (T-like) to nylon wool. The adherent cells resemble mammalian B lymphocytes and bear homologous human T cell receptor (beta chain) to a higher degree than T-like cells which resemble T lymphocytes.     

Identification of a macrophage-like mSubset in the axial organ sea star Asterias rubens.

The axial organ of the sea star Asterias rubens is a primitive immune organ. In addition to T and B-like cells phagocytic cells were also identified. In this report we demonstrate that these cells can be identified using immunocytochemistry together with the mouse to human monoclonal antibody CD68 KP1, normally used as a macrophage marker.     

Specific immune response in the sea star Asterias rubens: production of "antibody-like" factors

Axial organ cells from the sea star (Asterias rubens) inoculated 7 days before with TNP- or FITC-haptenated PAA beads and subsequently stimulated in vitro with the same antigen, produced and released a specific, soluble "antibody-like" substance that induced lysis of haptenated sheep erythrocytes. Fresh normal rabbit or guinea pig serum was essential for the lysis, suggesting the participation of complement components. The factor was produced by the total population of axial organ cells but not by nylon-wool adherent (B-like) or nonadherent (T-like) cells. These results provide further evidence of the existence, in the sea star, of a primitive immune system with characteristics reminiscent of the immune system of vertebrates.     

In vitro effect of various mitogens on starfish (Asterias rubens) axial organ cells

The effects of various mitogens on axial organ (AO) cells of the sea star have been studied. Pokeweed mitogen (PWM) stimulates [³H]thymidine incorporation by the whole population of axial organ cells of the sea star. This effect occurs 24 hr after the addition of PWM and is maximal at 40 μg/ml. In contrast, no stimulation is observed when coelomocytes are treated with PWM under the same conditions. No stimulation of the whole AO cell population is observed in the presence of Con A or LPS. However, the AO cell population can be divided, on the basis of surface adherence properties, into two subpopulations, adherent and nonadherent. Con A stimulates the nonadherent cells, but not the adherent cells: The stimulating effect is maximal 24 hr after addition of Con A and at 0.2–0.5 μg/ml. In contrast, LPS stimulates the adherent but not the nonadherent cells and the stimulating effect is maximal at 24 hr and at 45 μg/ml.     

In vitro effect of silica on axial organ cells in the presence and absence of mitogens

The axial organ (AO-cells) of the sea star Asterias rubens is a primitive immune organ. The total population was fractionated into two populations: adherent (B-like) and non-adherent (T-like) to nylon wool. Mitogenic responses were tested in the presence or absence of silica. Silica inhibits specifically the action of phagocytes contained in T-like and B-like subpopulations. Mitogenic responses do not occur in the presence of silica.     

Comparative analysis of behavior and proliferative activity in culture of cells of coelomic fluid and of cells of various tissues of the sea star <Emphasis Type="Italic">Asterias rubens</Emphasis> L. Isolated from normal and injured animals

The sources of coelomocytes in Asteroidea are suggested to be the coelomic epithelium, the axial organ, or Tiedemann’s bodies. To study the problem of whether the cells are replenished at the expense of divisions, we analyzed the incorporation of bromodeoxyuridine (BrdU) in vivo into cells from different tissues of the sea star Asterias rubens L. To study differentiation in vitro, methods of isolating and cultivating cells from various tissues were elaborated and an analysis of the behavior and incorporation of BrdU in culture was performed. The reproduced BrdU incorporation was detected in coelomic epithelial cells. The behavior of coelomocytes and the coelomic epithelial cells in culture depended on the time after the injury of the animals in which the cells were isolated, whereas, for the axial organ and Tiedemann’s bodies, no differences were revealed. After 2 months of cultivation, the formation of BrdU-incorporating, colony-like cells with high nuclear-cytoplasmic ratios was characteristic of coelomic epithelial cells. Thus, the most prospective object for studying the processes of A. rubens cell differentiation in vitro seems to be the coelomic epithelium.     

Podocytes in the axial organ of echinoderms

The axial organ of two sea urchin genera, Echinometra and Eucidaris , has been analysed with the electron microscope. It is mainly built up by an extracoelomic tissue rich in various leucocytic cells and blood vessels lacking an endothelium. The axial sinus (axocoel) is located on the interior of the axial organ, and evaginations extend into this loosely constructed tissue. The epithelium of the axial sinus and its extensions are characterized by epitheliomuscular cells and abundant podocytes, which overlie the blood vessels. Since podocytes are the well known structural basis for ultrafiltration, it is postulated that this is a function of the axial organ at least in echinoids and asteroids.     

Effect of silica on the spontaneous cytotoxicity of axial organ cells from Asterias rubens.

Axial organ cells (A.O.) which are composed of phagocytes and lymphocytes from the sea star Asterias rubens exert a spontaneous cytotoxicity against mouse tumour cells. This toxicity was tested in the presence or absence of silica. It appears that phagocytes play the role of killer cells.     

Production of an antibody-like factor in the sea star Asterias rubens: Role of the gastric haemal tufts

Cells from the axial organ (AO) of sea stars stimulated “in vivo” with TNP coupled to polyacrylamide beads and subsequently cultured “in vitro” were able to produce an antibody-like factor which induced the lysis of mammalian red cells sensitized with TNP. Three types of cells at least are involved in the production of the antibody-like factor. The addition of 2-mercapto-ethanol to the cultures including these 3 populations was essential but what is a novelty is the fact that cells from the gastric haemal tufts (G.H.T.), probably phagocytes, are able to replace it. Otherwise G.H.T. contain cells playing the role of nylon wool- non adherent AO cells or T like cells.     

Ultrastructural evidence of the excretory function in the asteroid axial organ (Asteroidea,Echinodermata)

The ultrastructure of the axial organ of Asterias amurensis has been studied The organ is a network of canals of the axial coelom separated by haemocoelic spaces. The axial coelom is lined with two types of monociliary cells: podocytes and musculo-epithelial cells. Podocytes form numerous basal processes adjacent to the basal lamina on the coelomic side. Musculo-epithelial cells form processes running along the basal lamina. Some bundles of these processes wrapped in the basal lamina pass through haemocoelic spaces between neighboring coelomic canals. It is hypothesized that the axial organ serves for filtration of fluid from haemocoelic spaces into the axial coelom cavity, from which urine is excreted through the madreporite to the exterior.     

A non‐lethal method for estimation of gonad and pyloric caecum indices in sea stars

Abstract. Gonad and pyloric caecum indices are widely used indicators of reproductive effort and nutritional condition in asteroids. Current methods of quantification generally require sacrificing multiple animals and the resulting reduction in local sea star density could have an unintended impact on benthic communities. Using the intertidal sea star Pisaster ochraceus, we developed and tested a method for estimating organ indices through the non‐lethal sampling of single arms. Indices estimated via dissections of single arms accurately predicted the values obtained by sacrificing whole animals. In laboratory and field trials, we compared two methods of sampling single arms: (1) arm removal, and (2) organ extraction through an incision (without arm removal). Two years after these treatments, organs had regenerated in the affected arms of most sea stars, but were small relative to those in unmanipulated arms. The extent of organ recovery did not differ between the two treatments, but sea stars in the arm removal group were relocated in the field more frequently than those in the arm incision group. Our results suggest that sampling via the removal of single arms can be an effective, non‐lethal method for estimating gonad and pyloric caecum indices in asteroids.     

Dysferlin is essential for endocytosis in the sea star oocyte

Dysferlin is a calcium-binding transmembrane protein involved in membrane fusion and membrane repair. In humans, mutations in the dysferlin gene are associated with muscular dystrophy. In this study, we isolated plasma membrane-enriched fractions from full-grown immature oocytes of the sea star, and identified dysferlin by mass spectrometry analysis. The full-length dysferlin sequence is highly conserved between human and the sea star. We learned that in the sea star Patiria miniata, dysferlin RNA and protein are expressed from oogenesis to gastrulation. Interestingly, the protein is highly enriched in the plasma membrane of oocytes. Injection of a morpholino against dysferlin leads to a decrease of endocytosis in oocytes, and to a developmental arrest during gastrulation. These results suggest that dysferlin is critical for normal endocytosis during oogenesis and for embryogenesis in the sea star and that this animal may be a useful model for studying the relationship of dysferlin structure as it relates to its function.     

Suppressor of Hairless, the Drosophila homolog of the mouse recombination signal-binding protein gene, controls sensory organ cell fates.

Suppressor of Hairless (Su(H)) is required at two stages of adult sensory organ development in Drosophila. Complete loss of Su(H) function results in a "neurogenic" phenotype in imaginal discs, in which too many cells adopt the sensory organ precursor cell fate. Su(H) is also involved in controlling the fates of sensillum accessory cells and is specifically expressed in two of these cells. Su(H) is the Drosophila homolog of the mouse J kappa RBP gene, whose product binds specifically to the recombination signal sequence of immunoglobulin J kappa segments. The Su(H) and J kappa RBP proteins are 82% identical over most of their length, and share with bacteriophage integrates and yeast recombinases a motif that includes residues directly involved in catalyzing recombination.     

Development and morphology of ciliary urns in the sea cucumber Synaptula hydriformis (Echinodermata: Holothuroidea)

Sea cucumbers (holothuroids) lack the only known echinoderm immune organ, the axial organ. Holothuroids of the families Synaptidae and Chiridotidae have coelomic organs, known as ciliary urns, that gather and excrete waste and, therefore, might function in immunity. Although ciliary urns are widely reported and illustrated in the literature, the process and histology of urn development remain unknown. Development and structure of ciliary urns were examined in Synaptula hydriformis using scanning electron, brightfield, and scanning laser confocal microscopy. Mature urns occurred on all three mesenteries in 10‐tentacled young and later growth stages, and developing urns were found in post‐pentactulae, 10‐tentacled young, and released juveniles. Developing urns were circular clusters of ciliated collar cells protruding from the mesentery. The cells increased in number to form the sessile cushion stage with a shallow lumen. The subsequent spoon‐shaped stage had a stalk and a deepened lumen with an extensive ciliary field where coelomocytes began to accumulate. Mature urns had a thin stalk and cornucopia‐shaped body with an abluminal epithelium of squamous cells and an adluminal epithelium of densely packed ciliated collar cells. Cell boundaries of the rim of mature urns and of the stalk and body of developing urns were outlined on one or both sides by microvilli and an elevated cell membrane. Ciliary urns resembling the cushion‐stage urns of S. hydriformis have been described in the sea star Archaster typicus. If urns in these groups are homologous, it is likely that cushion urns are plesiomorphic and that they are present and have been overlooked in other echinoderms.