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首页> 外文期刊>Trees. Structure and Function >Effects of Yariv dyes, arabinogalactan-protein binding reagents, on the growth and viability of Brazilian pine suspension culture cells
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Effects of Yariv dyes, arabinogalactan-protein binding reagents, on the growth and viability of Brazilian pine suspension culture cells

机译:Yariv染料,阿拉伯半乳聚糖蛋白结合剂,对巴西松树悬浮培养细胞生长和活力的影响

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摘要

Arabinogalactan-proteins (AGPs) are a family of highly glycosylated hydroxyproline-rich glycoproteins implicated in several aspects of plant growth and development. (o-d-glucosyl) Yariv phenylglycoside (o-GlcY), commonly known as Yariv reagent, selectively binds AGPs. We treated cell suspension cultures of Araucaria angustifolia, the Brazilian pine, with o-GlcY and observed inhibition of biomass increase in a culture medium with 50 oM o-GlcY. However, the growth was not inhibited by (l-d-galactosyl) Yariv phenylglycoside (l-GalY) which does not bind AGPs. Fluorescein diacetate staining of cells indicated that o-GlcY severely affected cell viability. However, cell swelling, bursting and release of cellular contents, all characteristics of necrotic cell death, were not observed in o-GlcY-treated cells. Instead, programmed cell death (PCD) structural changes such as cytoplasmic shrinkage and condensation were observed in o-GlcY-treated cells. In addition, callose accumulation, which is another marker of PCD, was also observed in o-GlcY-treated cells. The use of both, Ac-VEID-CHO, an inhibitor of caspase-like proteolytic activity related to PCD, and phenyl methyl sulphonyl fluoride (PMSF), a protease inhibitor known to suppress PCD, in the culture medium did not reverse the growth inhibition caused by o-GlcY. These data indicate that the o-GlcY-induced inhibition of Araucaria cell's growth is related to AGP perturbation, and also that this growth inhibition is due to increased cell death not driven by necrosis.
机译:阿拉伯半乳聚糖蛋白(AGPs)是一类高度糖基化的富含羟脯氨酸的糖蛋白,涉及植物生长和发育的多个方面。 (o-d-葡萄糖基)Yariv苯基糖苷(o-GlcY),通常称为Yariv试剂,可选择性结合AGP。我们用o-GlcY处理了巴西松南洋杉的细胞悬浮培养物,并观察到在含有50 oM o-GlcY的培养基中生物量增加的抑制作用。但是,生长不受未结合AGP的(1-d-半乳糖基)Yariv苯基糖苷(1-GalY)的抑制。细胞荧光素二乙酸盐染色表明o-GlcY严重影响了细胞活力。然而,在o-GlcY处理的细胞中未观察到细胞膨胀,细胞内含物的破裂和释放,坏死细胞死亡的所有特征。而是在o-GlcY处理的细胞中观察到程序性细胞死亡(PCD)结构变化,例如胞质收缩和浓缩。此外,在o-GlcY处理的细胞中也观察到了PCD的另一个标志物call质积累。在培养基中使用Ac-VEID-CHO(一种与PCD相关的caspase样蛋白水解活性的抑制剂)和苯基甲基磺酰氟(PMSF)(一种已知抑制PCD的蛋白酶抑制剂)在培养基中均不能逆转生长抑制作用由o-GlcY引起。这些数据表明,o-GlcY诱导的南洋杉细胞的生长抑制与AGP摄动有关,而且这种生长抑制是由于细胞死亡增加而不是由坏死驱动。

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