No abstract available

[en] The purpose of this study is to investigate the mechanism of inhibition of chondrogenic differentiation by X-irradiation. Cultures of chick limb bud mesenchymal cells were exposed to various dose of X-ray and chondrogenesis was examined. X-irradiation inhibited accumulation of proteoglycan based on the observation of alcian blue staining and expression of chondorcyte specific-type II collagen. X-irradiation also inhibited expression of protein kinase Ca while expression of PKCλ(ι, ε was not altered. Expression of Erk-1 was not changed by X-irradiation but phosphorylation of Erk-1 was increased. In addition, inhibition of Erk-1 phosphorylation by PD98059 overcame inhibitory effect of X-irradiation on the chondrogenic differentiation. PNA staining data showed that X-irradiation inhibited cellular aggregation. Taken together, these results suggest that X-irradiation inhibits chondrogenic differentiation by inhibiting cellular aggregation and suppressing expression of PKCa and promoting phosphorylation of Erk-1. In addition to above pathway, our results also suggest that X-irradiation may exerts its inhibitory effect by another signaling pathways

[en] Radiosensitivity tests on Hevea brasiliensis using 996 budded stumps of the clone RRIM 600, 235 pieces of budwood of PRIM 905 and 1000 seeds of RRIM 623 were carried out at the Rubber Research Institute Experimental Station, Sungai Buloh, Selangor. Irradiation using gamma rays from 1 to 10 krad showed that a dose of 2 krad proved lethal to budwood and 5 krad to seeds. Budded stumps were found to withstand up to 10 krad radiation. However, budbreak (sprouting) was observed only with radiation of up to 6 krad. At 7 krad, and above, the buds were either dead or remained dormant, although dormancy could be overcome partially with dikegulac sodium. For irradiation purposes, the survival of advanced planting material such as budded stumps was better than that of budwood. The percentage survival after irradiation was higher in budded stumps than in the other two materials; thus, a higher population was available for subsequent screening. (author). 6 refs, 2 figs, 2 tabs

No abstract available

[en] Bitter taste avoidance behavior (BAB) plays a fundamental role in the avoidance of toxic substances with a bitter taste. However, the molecular basis underlying the development of BAB is unknown. To study critical developmental events by which taste buds turn into functional organs with BAB, we investigated the early phase development of BAB in postnatal mice in response to bitter-tasting compounds, such as quinine and thiamine. Postnatal mice started to exhibit BAB for thiamine and quinine at postnatal day 5 (PD5) and PD7, respectively. Histological analyses of taste buds revealed the formation of microvilli in the taste pores starting at PD5 and the localization of type 2 taste receptor 119 (TAS2R119) at the microvilli at PD6. Treatment of the tongue epithelium with cytochalasin D (CytD), which disturbs ACTIN polymerization in the microvilli, resulted in the loss of TAS2R119 localization at the microvilli and the loss of BAB for quinine and thiamine. The release of ATP from the circumvallate papillae tissue due to taste stimuli was also declined following CytD treatment. These results suggest that the localization of TAS2R119 at the microvilli of taste pores is critical for the initiation of BAB.

[en] Several RNAs, including rRNAs, snRNAs, snoRNAs, and some mRNAs, are known to be localized at specific sites in a cell. Although methods have been established to visualize RNAs in a living cell, no large-scale visual screening of localized RNAs has been performed. In this study, we constructed a genomic library in which random genomic fragments were inserted downstream of U1A-tag sequences under a GAL1 promoter. In a living yeast cell, transcribed U1A-tagged RNAs were visualized by U1A-GFP that binds the RNA sequence of the U1A-tag. In this screening, many RNAs showed nuclear signals. Since the nuclear signals of some RNAs were not seen when the U1A-tag was connected to the 3' ends of the RNAs, it is suggested that their nuclear signals correspond to nascent transcripts on GAL1 promoter plasmids. Using this screening method, we successfully identified two novel localized mRNAs, CSR2 and DAL81, which showed bud-tip localization

[en] Bud burst is one of the most observable phenological stages in tree species, and its responses to environmental factors are found to be species-specific. Nevertheless, for dioecious plants, whether the bud burst responses are sex specific remains an open question, as do the underlying physiological mechanisms. Here, we investigated the effect of elevated temperature (+2 °C) and drought (30% field capacity) during December--March on bud development, gas exchange, water and nitrogen status, and carbohydrate metabolism in female and male Populus cathayana to understand how nongrowing season warming and drought modifies physiological and phenological traits. Our results showed that at ambient temperature, males experienced earlier bud burst than females. Winter warming significantly delayed bud burst and even synchronized it for both sexes because of the greater responsiveness of males. Although drought exerted little effect on the timing of bud burst, it significantly reduced bud fresh mass and limited bud growth by decreasing gas exchange capacity and nonstructural carbohydrate (NSC) accumulation; moreover, females were more affected by drought stress. The significant sex x watering x temperature interactions for δ¹³C and NSC indicate that sexual dimorphism in these condition-specific traits would increase along the environmental gradients, implying contrasting life history strategies in different ecological scenarios. The convergence in the time for bud burst caused by elevated temperature might exaggerate the competition among males, thus influencing the sex ratio, structure, and functioning of P. cathayana populations. (author)

[en] Balloon-occluded trans arterial chemo embolization (B-TACE) using a micro balloon catheter is a promising method for improvement of lipiodol emulsion accumulation and local control relative to conventional trans arterial chemo embolization. This method has been referred to as the balloon anchor technique in previous reports. We report a new technique for successful parent catheter advancement for achievement of stable backup for the selective insertion of a micro balloon catheter during B-TACE using the micro balloon as an anchor, even in patients with tortuous anatomy of the hepatic and celiac arteries. Deep Catalonian of parent catheters was accomplished in all three cases and complications such as vascular injury were not observed in the post procedure angiograms.

[en] Zebrafish pectoral fin bud formation is an excellent model for studying morphogenesis. Fibroblast growth factors (Fgfs) and sonic hedgehog (shh) are essential for pectoral fin bud formation. We found that Fgf16 was expressed in the apical ectodermal ridge (AER) of fin buds. A knockdown of Fgf16 function resulted in no fin bud outgrowth. Fgf16 is required for cell proliferation and differentiation in the mesenchyme and the AER of the fin buds, respectively. Fgf16 functions downstream of Fgf10, a mesenchymal factor, signaling to induce the expression of Fgf4 and Fgf8 in the AER. Fgf16 in the AER and shh in the zone of polarizing activity (ZPA) interact to induce and/or maintain each other's expression. These findings have revealed that Fgf16, a newly identified AER factor, plays a crucial role in pectoral fin bud outgrowth by mediating the interactions of AER-mesenchyme and AER-ZPA

[en] This paper details the development and verification of ROSESIM, a computer simulation model of the growth of ‘Royalty’ roses (Rosa hybrida L.) based on experimentally observed growth responses from pinch until flowering under 15 combinations of constant photosynthetic photon flux (PPF), day temperature (DT), and night temperature (NT). Selected according to a rotatable central composite design, these treatment combinations represent commercial greenhouse conditions during the winter and spring in the midwestern United States; each selected condition was maintained in an environmental growth chamber having 12-hour photoperiods. ROSESIM incorporates regression models of four flower development characteristics (days from pinch to visible bud, first color, sepal reflex, and flowering) that are full quadratic polynomials in PPF, DT, and NT. ROSESIM also incorporates mathematical models of nine plant growth characteristics (stem length and the following fresh and dry weights: stem, leaf, flower, and total) based on data recorded every 10 days and at flowering. At each design point, a cubic regression in time (days from pinch) estimated the plant growth characteristics on intermediate days; then difference equations were developed to predict the resulting daily growth increments as third-degree polynomial functions of days from pinch, PPF, DT, and NT. ROSESIM was verified by plotting against time each simulated plant growth characteristic and the associated experimental observations for the eight factorial design points defining the region of interest. Moreover, one-way analysis of variance procedures were applied to the differences between ROSESIM predictions and the corresponding observed means for all 15 treatment combinations. At 20 days from pinch, significant differences (P < 0.05) were observed for all nine plant growth characteristics. At 30 and 40 days from pinch, only flower fresh and dry weights yielded significant differences; at flowering, none of the 13 selected responses yielded significant differences. These graphical and statistical comparisons provide good evidence of ROSESIM’s ability to predict the growth response of ‘Royalty’ roses over a wide range of constant environmental conditions. (author)