The biological effect of sodium butyrate (NaBT) on SGC-7901 cells

Changes of (Na+-K+)-ATPase activity, cAMP and fibronectin (FN) content and cell surface microvilli were studied cytochemically, immunocytochemically and scanning electron microscopically on human stomach Glandular carcinoma (SGC-7901) cells treated with NaBT(2.5 mM). It was found that NaBT not only inhibited cell growth but also remarkably decreased the activity of cell surface (Na+-K+)-ATPase of SGC-7901 cells. Note worthy was that, in comparison with the untreated tumor cells, the increase of the intensity of intracellular cAMP and FN immunofluorescence in NaBT-treated tumor cells was striking. Moreover, in contrast to untreated tumor cells, the cell surface of NaBT-treated tumor cells showed more smooth and fewer microvilli under SEM. That NaBT may induce differentiation of SGC-7901 cells through inhibition of (Na+-K+)-ATPase activity and modulation of cellular cAMP and FN content was discussed.     

MPTP与帕金森氏症

1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)是一种神经毒,在人和灵长类动物,它选择性损害黑质纹体系统多巴胺神经元,使多巴胺(DA)及其代谢产物降低,引起典型的帕金森氏样症状。MPTP类毒性物质有其构效关系,其毒性主要与在脑内形成1-甲基-4-苯吡啶(MPP~ )有关。正常存在于脑内的色氨衍生物2-N-甲基四氢β-卡啉(2M-THBC),其构造及作用均类似于MPTP样物质,由此可以推断,MPTP除作为部分帕金森氏症的直接诱发原因外,极有可能是揭示原因不明的原发性帕金森氏病发病机理的一条重要途径。     

白百利烟草愈伤组织细胞细胞分裂素结合蛋白的研究

利用BA-Sepharose 4B亲和层析技术丛白百利烟草(Nicotiana tabacum Baibaili)愈伤组织细胞分离提纯了分子量为4400±100道尔顿的细胞分裂素结合蛋白(CB-蛋白)。在细胞表面、核糖体、线粒体、叶绿体和细胞核上以及在细胞液中都有CB-蛋白存在,而核糖体上的CB-蛋白含量量高。探讨了CB-蛋白的功能。     

中国连香树科的系统研究——Ⅰ.叶的宏观结构及叶柄维管束变化

本文研究了连香树科(Cercidiphyllaceae)叶的宏观结构,首次报道连香树齿腺体显微结构及晶体类型,并对叶柄维管束的变化作了进一步研究。通过与近缘科的比较,我们认为连香树科的系统演化处于孤立地位,和金缕梅科有较近的亲缘关系,与木兰科较为疏远。     

长期低浓度SO2对大豆生长和产量的影响

随着化石燃料消耗量不断增加,由此产生的主要大气污染物之一SO_2的浓度和影响范围也日趋增大。SO_2对植物,特别是对农作物的影响已受到普遍重视。本研究选择我国北方种植面积大、分布广的大豆为供试作物,在野外开顶式熏气装置中进行低浓度SO_2长期暴露试验,观察SO_2对大豆生长发育及产量的影响,以期为制订农田大气环境质量标准提供有一定参考价值的生态学基准。     

内蒙古自治区螽亚目(Tettigoniodea,Orthoptera)昆虫区系及地带性分布的研究

内蒙古自治区目前共知螽亚目昆虫5科、26属、58种(表1)。其中螽斯占总种数的74.2％,蟋蟀占17.3％,其余的占7.5％。其区系组成以古北种为主体,特别是东北中国种、东西伯利亚——蒙古种和欧洲——西伯利亚种是区系组成的核心(表2)。特有种占有一定的比例(10.3％),主要分布于该区东北部的森林草原亚带和西部的荒漠带。中部地区有部分华北种的渗入。在本区东部的草原带中,螽斯亚科昆虫最为丰富;西部的荒漠带中,硕螽亚科昆虫是最突出的代表种,并有中亚种的分布(表4)。从总的种类分布来看,东北部的森林带和草原带的昆虫种类明显比西部荒漠带要丰富,中部的干草原亚带则是上述两者的过渡区域。 文中还根据螽亚目昆虫在不同植被地区的分布情况,采用Sφgrensen系数比较了各地带之间昆虫区系的相似性(表3)。用聚类分析的方法将10个植被地带或亚带划分成6个大的地带区:森林区、草原区、荒漠区、暖温型森林草原区、暖温型典型草原区和暖温型荒漠草原区(图2)。作者详细地叙述了各个地带区中昆虫区系的组成特点和分布规律。并就前人对该区昆虫区划工作提出了若干修订意见。     

含甲肝病毒基因的重组痘苗病毒在动物体内产生针对甲肝病毒的中和抗体

用DNA重组技术得到的含甲肝病毒基因的重组痘苗病毒,可在家兔体内产生ELISA竞争抑制与中和抗体。基础免疫后,动物体内竞争抑制抗体滴度为10,加强免疫后达到80。由重组病毒产生的抗体中和指数比甲肝病毒产生者略低。     

化学法合成生物素标记寡核苷酸探针

 生物素可通过氨烷基磷酰胺基团连接到寡核苷酸5'末端,反应在水溶液中进行,核苷酸的侧链基团不用保护。我们以这种化学法合成了生物素标记的寡核苷酸探针,其显色灵敏度达50pg,杂交灵敏度达0.4fmol,并与酶标生物素寡核苷酸探针进行了比较,也对两种不同显色体系作了比较。     

Separate functional domains of the herpes simplex virus type 1 protease: evidence for cleavage inside capsids.

The herpes simplex virus type 1 (HSV-1) protease (Pra) and related proteins are involved in the assembly of viral capsids and virion maturation. Pra is a serine protease, and the active-site residue has been mapped to amino acid (aa) 129 (Ser). This 635-aa protease, encoded by the UL26 gene, is autoproteolytically processed at two sites, the release (R) site between amino acid residues 247 and 248 and the maturation (M) site between residues 610 and 611. When the protease cleaves itself at both sites, it releases Nb, the catalytic domain (N0), and the C-terminal 25 aa. ICP35, a substrate of the HSV-1 protease, is the product of the UL26.5 gene. As it is translated from a Met codon within the UL26 gene, ICP35 cd are identical to the C-terminal 329-aa sequence of the protease and are trans cleaved at an identical C-terminal site to generate ICP35 e,f and a 25-aa peptide. Only fully processed Pra (N0 and Nb) and ICP35 (ICP35 e,f) are present in B capsids, which are believed to be precursors of mature virions. Using an R-site mutant A247S virus, we have recently shown that this mutant protease retains enzymatic activity but fails to support viral growth, suggesting that the release of N0 is required for viral replication. Here we report that another mutant protease, with an amino acid substitution (Ser to Cys) at the active site, can complement the A247S mutant but not a protease deletion mutant. Cell lines expressing the active-site mutant protease were isolated and shown to complement the A247S mutant at the levels of capsid assembly, DNA packaging, and viral growth. Therefore, the complementation between the R-site mutant and the active-site mutant reconstituted wild-type Pra function. One feature of this intragenic complementation is that following sedimentation of infected-cell lysates on sucrose gradients, both N-terminally unprocessed and processed proteases were isolated from the fractions where normal B capsids sediment, suggesting that proteolytic processing occurs inside capsids. Our results demonstrate that the HSV-1 protease has distinct functional domains and some of these functions can complement in trans.