Graph-Theoretical Analysis of Cleavage Pattern: Graph Developmental System and Its Application to Cleavage Pattern of Ascidian Egg

The skeletal structure of the embryo is represented by the graph. In the graph, the cells and the connectivities between the cells are reduced to the nodes and edges, respectively. Along cleavage history, the series of graphs is obtained. In this paper I propose a new graph developmental system(GDS) which develops the series of graphs. And I represent and analyze the cleavage pattern of the ascidian egg by GDS. In order to represent it by GDS, at first, the connectivities between the cells are labeled according to the developments of the connectivities at the next time step, and next the cells are labeled. But there are two ways of labeling the cells, then two types of GDS are defined: (1) to label according to the pattern of the connectivities of their descendant cells after two time steps (G-GDS), (2) to label according to the cell fates (C-GDS). The C-GDS of the ascidian egg produces 16 cleavage patterns at 64-cell stage non-deterministically. If some labels are distinguished at 16-cell stage, the C-GDS becomes deterministic at 64-cell stage.
GDS will be useful to simulate morphogenesis by the computer graphics.     

K-Casein Suppresses Melanogenesis in Cultured Pigment Cells

The effects of bovine milk proteins on melanogenesis in B16 cells were examined. Both whey protein isolate and casein exhibited depigmenting properties. Among the major protein components of milk—including β-lactoglobulin, α-lactalbumin, α-, β-, and k-casein—only K-casein exhibited the depigmenting effect. However, the carboxyl terminal peptide of K-casein, glycomacropeptide, did not show this activity. Also, K-casein promoted the proliferation of the cells and inhibited the activity of tyrosinase in the cells. These results indicate that K-casein acts as a melanogenesis-suppressing modulator.     

喜马拉雅灰包菇──相传是“喜马拉雅雪人”的一种食物

喜马拉雅灰包菇ＳｅｃｏｔｉｕｍｈｉｍａｌａｉｃｕｍＺａｎｇｅｔＤｏｉ,由Ｄｒ．ＴｅｉｚｏＯｇａｗａ采于尼泊尔境内的喜马拉雅山带,据当地居民云：该菌为喜马拉雅雪人的一种食物。所谓雪人可能是高山雪线一带的动物。本文对该菌的分类特征和雪人的有关讨论作了介绍。原模式存日本国立科学博物馆。     

Establishment of the Embryo-derived Stem (ES) Cell Lines from Mouse Blastocysts: Effects of the Feeder Cell Layer.

The ES ceii lines are embryo-derived stem cell lines directly isolated from the inner cell mass of mouse blastocysts using feeder cell layer. We have established a number of ES cell lines from 129 or C57BL/6 strain mice by using the feeder layer of the STO cells (from ATCC) or the primary embryonic fibroblasts, which was obtained by trypsinizing the 16-day-old BALB/c mouse fetus. The ES cell lines established on the STO feeder layer showed differentiation into various tissues in solid tumors when injected into syngenic mice. Karyotype was, however, nearly tetraploid. The ES cell lines established on the primary fibroblasts exhibited differentiation into larger variety of tissues in solid tumors. Karyotype was almost diploid and majority of the cells kept normal set of chromosomes in G-banding. We conclude that the primary fibroblasts are better feeder layer than the STO cells for establishment and maintenance of the ES cell lines.     

Enhanced Melanogenesis Induced by Tyrosinase Gene-Transfer Increases Boron-Uptake and Killing Effect of Boron Neutron Capture Therapy for Amelanotic Melanoma

Specific and powerful cancer killing effect for melanoma by boron neutron capture therapy (BNCT) using DOPA analogue, ¹⁰B-p-boronophenylalanine (¹⁰B-BPA), has been established, but amelanotic melanoma is insufficiently responsive to ¹⁰B-BPA BNCT in comparison with actively melanin-producing melanoma. Although the accumulation mechanism of ¹⁰B-BPA within melanoma was not established, we have recently obtained findings suggesting that melanin monomers, key intermediates for melanin polymer formation, play a critical role in ¹⁰B-BPA accumulation. In addition, there are some kinds of human amelanotic melanomas, such as MEL2A, in which expression of tyrosinase is repressed or lacking though tyrosinase-related protein (TRP)-l and TRP-2 are well expressed. Thus, by using a similarly tyrosinase-lacking mouse amelanotic melanoma cell line, A1059, we constructed TA1059 cells by transfecting human tyrosinase-cDNA into these cells. TA1059 cells acquired higher DOPA-oxidase and DOPAchrome tautomerase activity as well as eumelanin content at even higher levels than those of B16F10 cells. TA1059 cells showed about 2.5 times higher ^p-boronophenylalanine (BPA) uptake than A1059 cells in culture. In animal experiments, by using these cell lines, tumor growth of TA1059 was significantly suppressed by ¹⁰B-BPA BNCT as compared with A1059. These findings indicate that the induction of active melanin biosynthesis by melanogenic gene-transfer effectively improves the treatment of amelanotic melanoma by BNCT.     

Food plants and life cycle of Lymantria bantaizana Matsumura (Lepidoptera: Lymantriidae) in northern Honshu, Japan

The food plants and life cycle of Lymantria bantaizana were investigated in Iwate Prefecture, northern Honshu, Japan from 2000 to 2002. Eggs laid in July hatched approximately 10 days after oviposition. Hatched larvae fed only on Juglandaceae, Juglans mandshurica var. sachaliensis, J. regia var. orientalis and Pterocarya rhoifolia when reared in the laboratory. In field rearing, the plants of Juglans enabled the moth to complete its life cycle. Differing from all other known Lymantria species in Japan, the moth overwintered not in the egg stage but in the fifth or sixth instar larval stage. Lymantria bantaizana had eight larval instars in both sexes. Moth emergence occurred mostly in July at a field‐trapping site in Iwate Prefecture.     

Genetic diversity increases regional variation in phenological dates in response to climate change

Climate change is inducing changes in the phenological timings of organisms. Genetic diversity could influence phenological responses to climate change, but empirical evidence is very limited. We estimated the regional variation across Japan in flowering and leaf budburst dates of plants based on a dataset of phenological timings from 1953 to 2005. The observed plants' genetic diversities varied according to human cultivation. The within-species variations of phenological response to temperature as well as regional variations were less in the plant populations with lower genetic diversity. Thus, genetic diversity influences the variation in phenological responses of plant populations. Under increased temperatures, low variation in phenological responses may allow drastic changes in the phenology of plant populations with synchronized phenological timings. Our findings indicate that we should pay attention to maintaining genetic diversity of populations to alleviate changes in phenology due to future climate change.     

Diagnosing and assessing uncertainties of terrestrial ecosystem models in a multimodel ensemble experiment: 2. Carbon balance

This paper examines carbon stocks and their relative balance in terrestrial ecosystems simulated by Biome‐BGC, LPJ, and CASA in an ensemble model experiment conducted using the Terrestrial Observation and Prediction System. We developed the Hierarchical Framework for Diagnosing Ecosystem Models to separate the simulated biogeochemistry into a cascade of functional tiers and examine their characteristics sequentially. The analyses indicate that the simulated biomass is usually two to three times higher in Biome‐BGC than LPJ or CASA. Such a discrepancy is mainly induced by differences in model parameters and algorithms that regulate the rates of biomass turnover. The mean residence time of biomass in Biome‐BGC is estimated to be 40–80 years in temperate/moist climate regions, while it mostly varies between 5 and 30 years in CASA and LPJ. A large range of values is also found in the simulated soil carbon. The mean residence time of soil carbon in Biome‐BGC and LPJ is ～200 years in cold regions, which decreases rapidly with increases of temperature at a rate of ～10 yr °C^?1. Because long‐term soil carbon pool is not simulated in CASA, its corresponding mean residence time is only about 10–20 years and less sensitive to temperature. Another key factor that influences the carbon balance of the simulated ecosystem is disturbance caused by wildfire, for which the algorithms vary among the models. Because fire emissions are balanced by net ecosystem production (NEP) at steady states, magnitudes, and spatial patterns of NEP vary significantly as well. Slight carbon imbalance may be left by the spin‐up algorithm of the models, which adds uncertainty to the estimated carbon sources or sinks. Although these results are only drawn on the tested model versions, the developed methodology has potential for other model exercises.