Uneven distribution pattern and increasing numbers of mesenchyme cells during development in the starfish, Asterina pectinifera.

During development, the embryos and larvae of the starfish Asterina pectinifera possess a single type of mesenchyme cell. The aim of this study was to determine the patterns of behavior of mesenchyme cells during the formation of various organs. To this end, we used a monoclonal antibody (mesenchyme cell marker) to identify the distribution patterns and numbers of mesenchyme cells. Our results revealed the following: (i) mesenchyme cell behavior differs in the formation of different organs, showing temporal variations and an uneven pattern of distribution; and (ii) mesenchyme cells continue to be generated throughout development, and their numbers are tightly regulated in proportion to total cell numbers.

Effects of the fungicide ortho-phenylphenol (OPP) on the early development of sea urchin eggs.

In this study, we assessed the impact of imidazole fungicide ortho-phenylphenol (OPP) on the early development of a marine invertebrate, the sea urchin, a marine bioindicator. Fungicides are widely used and have been reported to accumulate not only in farm soil but also in freshwater and seawater sediments. Therefore, it is essential to clarify the effects of OPP on marine environments. Toxicity was estimated as the inhibition ratio of the 120 min-embryo and/or the 24 h-embryo development. The addition of OPP to embryos of the two sea urchin species, Scaphechinus mirabilis (S. mirabilis) and Strongylocentrotus nudus (S. nudus), at 0.1 mM or higher, resulted in acute toxicity (cell death). The IC50 value of the 120 min-embryos or the 24 h-embryos for S. mirabilis and S. nudus with OPP was around 0.06 mM, indicating that fertilized eggs and embryos of the sea urchin are more sensitive to OPP than higher vertebrates. In addition, in the presence of OPP (0.005-0.05 mM), the proportion (%) of the gastrula keeping the fertilization membrane increased, suggesting that OPP (0.005-0.05 mM) inhibited the hatching process, possibly by affecting the hatching enzyme activity.

Dynamics of Mitotic Apparatus Formation and Tubulin Content during Oocyte Maturation in Starfish: (tubulin/starfish/oocyte maturation/cytoskeleton/meiosis).

To follow the topo-temporal behavior of structures containing tubulin and the change in tubulin content during oocyte maturation, starfish oocytes were extracted with a medium containing detergent so that morphological observation and biochemical analysis could be conducted on the same residual oocyte preparation simultaneously. Before 1-methyladenine (1-MeAde) stimulation, "pre-meiotic asters" were observed on the germinal vesicle at the animal pole. 1-MeAde caused the appearance of distinct asters at the position of the aster precursor. When germinal vesicle breakdown (GVBD) took place, chromosomes were condensed. Chromosome gathering was concurrent with a reduction in the size of nuclear matrix. The mitotic apparatus was first constructed parallel to the cortex and then changed its axis perpendicularly. Fluorescence of tubulin due to indirect immunofluorescence in the cytoplasm other than the mitotic apparatus decreased rapidly along the course of maturation at least up to the first metaphase. Despite these dynamic morphological change, the tubulin content in the whole oocyte and the residual structures, measured by SDS-PAGE and immunostaining, did not show remarkable (statistically significant) changes through the course of maturation, although the content tended to decrease a little before the second polar body formation and to increase thereafter in the latter.

Presence of a Tetrahymena growth promoting activity in fetal bovine serum.

Treatment of cultures of the ciliate Tetrahymena with fetal bovine serum (FBS) enhanced the rate of cell proliferation. The growth promoting activity was partially purified from FBS as a high Mr complex including four components with apparent Mr values of 180 kDa, 68 kDa, 60 kDa and 30 kDa by a 4-step procedure. The 180 kDa component was identified by amino acid sequencing as α2-macroglobulin. The addition of purified α2-macroglobulin from bovine plasma to cultures of Tetrahymena was also found to enhance the rate of cell proliferation. This report is the first dealing with the direct identification of a mammalian factor which promotes the growth of free-living protozoa.

Changes in Intracellular Concentrations of Cyclic Nucleotides during the Initiation Process of Starfish Sperm Motility: (cAMP/cGMP/starfish/sperm/motility initiation).

Changes in the intracellular concentrations of cyclic nucleotides during the initiation of starfish sperm motility were examined. The intracellular concentration of cGMP decreased just after dilution of sperm with sea water, whereas that of cAMP increased concomitant with initiation of sperm motility. In acidic sea water, the intracellular concentration of cGMP decreased but no increase in that of cAMP was observed and sperm remained immotile. The presence of a phosphodiesterase inhibitor enhanced the rate of increase in the intracellular concentration of cAMP and the sperm motility. These results indicate that cAMP is involved in the initiation of sperm motility in starfish.