It is now well established that epithelial-mesenchymal interactions are essential for the formation of many organs in the development of the animals. Chicken digestive organs provide a valuable model system for analysis of the mechanisms underlying the epithelial-mesenchymal interactions. Here we will present our recent data indicating that the mesenchymal factors necessary for the epithelial differentiation in the chicken stomach are composed of several components such as growth factors and extracellular matrices. The possible involvement of bone morphogenetic protein-2 will be discussed.

The shift of chloride cell distribution was investigated during early life stages of seawater-adapted killifish (Fundulus heteroclitus). Chloride cells were detected by immunocytochemistry with an an-tiserum specific for Na , K -ATPase in whole-mount preparations and paraffin sections. Chloride cells first appeared in the yolk-sac membrane in the early embryonic stage, followed by their appearance in the body skin in the late embryonic stage. Immunoreactive chloride cells in the yolk-sac membrane and body skin often formed multicellular complexes, as evidenced by the presence of more than one nucleus. The principal site for chloride cell distribution shifted from the yolk-sac membrane and body skin during embryonic stages to the gill and opercular membrane in larval and later developmental stages. Our observations suggest that killifish embryos and newly-hatched larvae could maintain their ion balance through chloride cells present in the yolk-sac membrane and body skin until branchial and opercular chloride cells become functional.

Electromyographic recording was used to study how the activity of the eyestalk motor system is modified during the recovery of eyestalk posture following unilateral statolith removal in crayfish Procambarus clarkii Girard. Intact animals showed bilaterally balanced activity of the muscle 12 (eyecup-up muscle) in the upright body position. Body rolling caused an increase in the muscle activity on the lowered side and a decrease on the lifted side. Unilateral statolith removal caused imbalance in the bilateral muscle activity in the upright body position: the muscle 12 activity decreased tonically on the operated side and increased on the opposite side. Body rolling of the operated animal caused an increase in the muscle activity from the unbalanced level on the lowered side and a decrease on the lifted side. When the operated animal recovered its original symmetrical posture of eyestalks 14 days after operation, the muscle activity was found on both sides to return to the previous level observed before statolith removal, regardless of the post-operative condition in which the animal was maintained. In those animals that did not recover the original eyestalk posture, the unbalanced activity of bilateral muscles that was caused by unilateral statolith removal remained unchanged. The results indicate that the recovery of eyestalk posture is based on restoration of the original activity balance, rather than on fixation of the operation-induced activity imbalance, among bilaterally homologous sets of muscles in the course of central compensation.

Fine structure of the heart and the effects on the heartbeat of some transmitter candidates in crustacean cardioregulatory system were examined in the myogenic heart of the branchiopod crustacean Triops longicaudatus. Electron microscopy revealed that, in each myocardial cell, myofibrils are confined in the part facing the epicardium and intercalated disks are present between the myofibrillar regions of adjacent myocardial cells. No neural elements were found in the heart, suggesting lack of extrinsic cardioregulatory nerves from the central nervous system. Gamma aminobutyric acid and acetylcholine produced no detect-able changes in the myogenic activity of the heart at concentrations up to 10⁻³ M, respectively. Glutamate induced a depolarizing membrane response in the cardiac muscle with a threshold concentration of approximately 1×10⁻⁵ M. The amplitude of the depolarizing response was concetration-dependent and saturated at approximately 1×10⁻⁴ M. The myogenic activity of the heart increased in frequency with glutamate of less than approximately 3×10⁻⁵ M. With higher dose of glutamate, action potential adaptation occurred in the cardiac muscle and the heart exhibited a systolic arrest.

With the intention of simplifying construction and operation, improvements have now been made to a photoelectric system for measuring the motile responses of chromatophores. Introduction of chop-per-stabilized operational amplifiers with a complimentary metal-oxide semiconductor (C-MOS) input has brought about a much improved stability of the electronics. Such a feature has been found to be especially suitable for measurements requiring higher amplification and longer periods of time, e.g., the detection of the effects of various factors on bright-colored chromatophores. The use of appropriate color filters that limit the spectral range of light used for measurement has also proven to be important. By installing a small filter close to the photosensor, we can now record the responses of particular types of chromatophores more selectively, while visually monitoring the states of all kinds of chromatophores in natural color. To minimize the influence of motile activities of xanthophores and/or erythrophores, the use of an orange-to-red long-pass filter is appropriate to optimize recording the melanophore responses. By contrast, the responses of xanthophores or erythrophores can be recorded more easily by employing a violet-to-blue band-pass filter, because that increases the contrast of images of these cells against the background. Using an orange-red variety of the medaka Oryzias, we have also recorded photometrically the responses of leucophores, whose organelles are light-scattering. A long-pass filter was efficient in excluding the influences of co-existing xanthophores.

Genetic variations within a population of the Japanese sika deer, Cervus nippon, on Kinkazan Island were studied by microsatellite analysis. Seventeen pairs of polymerase chain reaction primers designed for several species of ungulates successfully amplified polymorphic microsatellite DNA in sika deer. About 20% of the Kinkazan population was sampled and genotyped for nine diagnostic microsatellite loci. Alleles at those loci in the Kinkazan population were found to be under the Hardy-Weinberg equilibrium. To determine whether the Kinkazan deer have a reduced level of genetic variability, an average heterozygosity in the population was calculated and compared with the values determined for other populations from Hyogo, Yamaguchi, Shimane, Tsushima, and Nagasaki. Neither the observed nor the expected heterozygosity in the Kinkazan deer significantly differed from that in the other populations. Our result indicated that, despite its small population size, the Kinkazan deer preserve extensive microsatellite variations.

An electrophoretic survey of allozyme variation was conducted in four, highly polymorphic loci on nine populations of ostracod Candona neglecta Sars from three different environments: the profundal of post-glacial lakes, deep muddy bottom of the Baltic Sea and small astatic water bodies. The results suggest lack of genetic isolation between populations from lake profundal and the Baltic Sea. On the other hand a very distinct founder effect can be noted in the case of young, isolated populations from small astatic basins. It is suggested that a population inhabiting a large lake may be genetically subdivided due to differentiated eutrophication.

Cell cultures are good in vitro model systems in place of using living animals. In the present study, we developed a simple culture method in which tissues were pretreated with a low concentration of sodium hypochlorite solution (NaClO) to prevent not only bacteria but also fungi. Scales removed from a goldfish (Carassius auratus) body were treated with 70% ethanol and then with 0.3% of sodium hypochlorite solution, and cultured in vitro in an atmosphere containing 0.5% CO₂. The doubling time of the established cells (GAKS)^† was 24 hr. The GAKS cells contained alkaline phosphatase activity (8.3±1.1 nmol/min/mg protein) and secreted 0.32±0.07 pg/ml endothelin during a 3 day culture of a full monolayer sheet.

To investigate whether a female sex steroid, estrogen, acts as a natural inducer of female gonadal sex determination (or ovary formation) in the medaka fish, Oryzias latipes, the effects of an aromatase inhibitor and anti-estrogens on sexual differentiation of gonads were examined. We found that both drugs did not show any discernible effects on the genetically determined sex differentiation in both sexes. However, the aromatase inhibitor impaired the paradoxical effects of androgen (a male sex steroid), and the anti-estrogens inhibited the male-to-female sex reversal caused by estrogen. Treatments of the fertilized eggs with androgen disturbed the gonadal sex developments in both sexes, suggesting that sex steroid synthesis is detrimental to the gonadal sex developments in the medaka embryos. These results are consistent with the previous observation that sex steroids are not synthesized before the onset of gonadal sex differentiation, and suggest that ovary formation in the genetic females of the medaka fish is not dependent on estrogen.

Effects of morning and evening injections of pineal 5-methoxyindoles (MI), melatonin (aMT) and 5-methoxytryptamine (MT), for 60 continuous days, were observed on the testes of sham-operated (SO) and pinealectomized (Px) Indian palm squirrel, Funambulus pennanti maintained under different photoperiods during the gonad active phase. Long photoperiod (LP) of 14L:10D appeared stimulatory to the testes and caused a significant increase in the weight and seminiferous tubule diameter of both SO and Px animals, as compared to the animals under natural day-length (NDL). Short photoperiod (SP) of 10L:14D had an inhibitory influence and reduced the testes weight and its tubule diameter. aMT and MT injections during evening hours significantly reduced testes weight and tubule diameter of SO and Px animals under NDL, LP and SP. However morning injections, under all conditions, were without any significant effect. The results suggest an inhibitory effect of aMT and MT, under above photoperiodic conditions, on the testes of this tropical mammal. The time of administration of the MI is important in the expression of the effect.

Many fertile individuals of the apodid holothurian Patinata ooplax, living in the intertidal area of the Ichiki Fishing Port in southern Kyushu, Japan, spawned during the two days after every full and new moon, probably the first and second days, in the period from the middle of July to the end of August during 1990, 1992 and 1993. Matured individuals were divided into three sexual types: males, hermaphroditic males with an early stage of oocytes, and females, using a dissecting microscope. The distribution frequency and gonadal histology of these sexual types indicate that some individuals changed from male to female or in the reverse direction at two-week intervals between spawnings, and suggest that some change first from male to female, and then back to male during the main breeding season. In addition, it was found that during the main breeding season, synchronous gametogenesis occurred in association with the sex changes, and that the period from the initiation of spermatogonia proliferation to sperm release during the same season was two weeks, and the period from the initiation of oocyte growth to egg shedding was probably slightly longer than two weeks.

The effect of a gonadotropin-releasing hormone (GnRH) agonist on luteinizing hormone (LH) receptor mRNA expression was examined histologically in the ovaries of immature hypophysectomized (HPX) rats by in situ hybridization. In the ovaries of HPX rats treated with diethylstilbestrol (DES) and pregnant mare serum gonadotropin (PMSG), LH receptor mRNA was expressed in the granulosa cells of mature follicles as well as the theca-interstitial cells. In DES-primed ovaries of rats treated with both GnRH agonist plus PMSG, many follicles were luteinized without ovulation, and the signal of LH receptor mRNA disappeared completely in the theca-interstitial cells as well as the luteinized cells, but remained in the granulosa cells of unaffected mature follicles. The complete suppression of the theca-interstitial LH receptor expression by GnRH agonist was also observed in HPX rats that received no other treatment. On the other hand, the coadministration of a GnRH antagonist with PMSG resulted in the hyperstimulation of follicular growth, accompanied by very strong expression of LH receptor mRNA in the granulosa cells as well as the thecainterstitial cells. In addition, morphological changes in the ovarian interstitial cells were also induced by the administration of GnRH agonist in HPX rats: loose connective tissue decreased and the interstitial cell mass markedly increased. The increase of the interstitial cells became more prominent when rats were treated with GnRH agonist and testosterone simultaneously. These results suggest that GnRH may be an important factor for modulating the interstitial cell function and differentiation in the rat ovary.

In order to compare ecdysone metabolism between diapause eggs and non-diapause eggs of the silkworm, Bombyx mori, ³H-ecdysone and its derivatives (³H-3-epiecdysone and ³H-ecdysone 22-phosphate) were injected into the eggs at various stages during early embryogenesis, and the resultant labelled metabolites were analyzed by high-performance liquid chromatography. From the quantitative and qualitative changes in the labelled metabolites between diapause eggs and non-diapause eggs, it was demonstrated that epimerization of ecdysone occurred during early embryogenesis irrespective of the embryonic stage in both diapause eggs and non-diapause eggs, and that phosphorylation of ecdysone was a major metabolic step in diapause eggs, whereas dephosphorylation of ecdysone 22-phosphate and its subsequent hydroxylation at the C-20 and C-26 positions were characteristic in non-diapause eggs.

We investigated the nucleotide sequences of cDNA fragments coding calcitonin from ultimobranchial glands in 2 species of urodelans (1 salamander and 1 newt) and 4 species of anurans (1 toad and 3 frogs) by the reverse transcription polymerase chain reaction (RT-PCR) method and rapid amplification of cDNA ends (RACE)-PCR method. The salamander and newt calcitonins were each 97% and 94% similar to the lungfish and caiman calcitonins that we have already reported, in the amino acid sequences. However, anuran calcitonins were not only dissimilar (63–81%) to the lungfish and caiman calcitonins but also diversified (59–91%) even among anurans. The sequence identity of toad calcitonin was always low (59–66%) among anurans.

The ontogeny of the caudal neurosecretory cells (Dahlgren cells) in the caudal spinal cord of the chum salmon, Oncorhynchus keta, was examined by conventional electron microscopy and with immunohistochemistry for urotensins (U) and neuropeptide Y (NPY). The precursors of the Dahlgren cells first appeared as agranular ovoid cells in the caudal region of the neural tube of 40-day-old embryos about one week before hatching. The occurrence of cytoplasmic granules in the immature Dahlgren cells became evident by the 14th day after hatching. At this moment, the U-positive reaction was merely demonstrated in some of the granules. Close association of NPY-positive fibers with the caudal neurosecretory structures was recognizable in 1-month-old larvae. Thus, it is apparent that the salmon Dahlgren cells start their secretory activity (production of the secretory granules) in early larval stages and that, thereafter, NPYergic afferent innervation of the caudal neurosecretory system becomes evident.

We compared primary and secondary structures of V4 (helices E23-2 to E23-5) and V7 (helix 43) regions of 18S rRNAs in insects and the other three major arthropod groups (crustaceans, myriapods, and chelicerates) known so far. We found that the lengths of primary sequences and the shapes of secondary structures of these two hypervariable regions of insect 18S rRNA even at infraclass levels are phylogenetically informative and reflect major steps in insect evolution. The long sequence insertion and bifurcated shape of helices E23-2 to E23-5 in the V4 region are unique synapomorphic characters for winged insects (Pterygota). The long sequence insertion and expanded stem length of helix 43 in the V7 region are synapomorphic characters for holometabolous insects which conduct complete metamorphosis. The strongly conserved secondary structures suggest the possibility that these hypervariable regions may be related with certain important cellular functions unknown thus far. The comparison with insect fossil records revealed that the pterygote synapomorphy (V4) and the holometabolous synapomorphy (V7) were established prior to the acquisition of insect wings (flight system) and prior to the development of complete metamorphosis, respectively. These synapomorphies have been also relatively stable over at least 300 Myr and 280 Myr, respectively as well. It implies that the expansion events of the V4 and V7 regions have not occurred simultaneously but independently at different periods during the insect evolution. Then this suggests that V4 and V7 regions are not functionally correlated as recently suggested by Crease and Coulbourn.

To elucidate the phylogenetic relationships among four species belonging to the genus Petaurista (P. alborufus castaneus, P. alborufus lena, P. leucogenys leucogenys, P. leucogenys nikkonis, P. petaurista melanotus, and P. philippensis grandis), we investigated the partial sequences (1,068 bp) of the mitochondrial cytochrome b gene for these giant flying squirrels. Phylogenetic trees (NJ, MP, and ML trees) constructed from cytochrome b sequences indicated that P. leucogenys was grouped independently with other species, and that P. philippensis was most closely related to P. petaurista with 99–100% bootstrap values. In addition, two subspecies of P. alborufus did not form a single clade: P. alborufus castaneus from China was most distantly related to the other species, whereas P. alborufus lena from Taiwan was closely related to P. petaurista and P. philippensis with 82–90% bootstrap values. This result suggests that it is reasonable to regard P. alborufus lena as a distinct species from P. alborufus castaneus.