化学合成siRNA抑制H5N1亚型禽流感病毒在鸡胚成纤维细胞中的增殖

为研究RNA干涉对H5N1亚型禽流感病毒的增殖抑制作用,针对H5N1亚型禽流感病毒的NP和PA基因,设计4对siRNA干涉序列,并将其转染到鸡胚成纤维细胞,6h后接种H5N1亚型禽流感病毒液,在病毒感染后的16～56h内测定细胞上清中的病毒血凝价及观察细胞病变,并在病毒感染36h后检测NP、PA、HA和β-actin基因的mRNA水平。结果显示4对siRNA均能不同程度地抑制H5N1亚型禽流感病毒在鸡胚成纤维细胞中的增殖,但以PA为靶基因设计的一对干涉序列效果最优;实验还证实随着时间的延长,干涉效应逐渐减弱。本实验为研究RNA干涉技术防控禽流感提供了依据。     

黄芪多糖对大鼠口腔溃疡治疗作用研究

本研究旨在探讨黄芪多糖对患有口腔溃疡大鼠(recurrent aphthous ulcer,RAU)的表皮细胞生长因子(epidermal growth factor,EGF)水平及T淋巴细胞亚群的影响。根据溃疡面的直径计算愈合率及HE染色观察溃疡组织病理学改变,酶联免疫吸附法(ELISA)测定EGF的水平,流式细胞仪检测大鼠外周血CD4+T细胞、CD8+T细胞亚群的百分率。实验结果显示治疗20 d后,黄芪多糖组大鼠溃疡面积减小,愈合率为87.5%～100%。与正常对照组相比,模型对照组大鼠CD4+T细胞数减少、CD8+T细胞数升高,CD4+/CD8+比值降低(P<0.05)。与模型对照组相比,黄芪多糖组大鼠外周血CD4+T细胞数升高、CD8+T细胞数降低,CD4+/CD8+比值回升(P<0.05)。EGF水平在造模后出现明显下降,黄芪多糖灌胃治疗后有升高。提示黄芪多糖能够提高RAU实验性大鼠EGF的水平和改善T细胞亚群的失衡状态,具有明显地促进口腔溃疡愈合的作用。     

Stem tissue mass density is linked to growth and resistance to a stem‐boring insect in Alternanthera philoxeroides

To investigate how stem anatomical structure is linked to growth and resistance to stem‐boring insects in a herbaceous species, six populations of alligatorweed (Alternanthera philoxeroides) were grown in a common garden. Stem growth rate (GR) of A. philoxeroides and pupation rate as an estimate of resistance to a stem‐boring insect (Agasicles hygrophila) were quantified. Stem tissue mass density (TMD) was measured and stem anatomical traits were analysed on cross‐sectional areas (CSA). Stem TMD was positively correlated with resistance (i.e. negatively correlated with pupation rate) and negatively correlated with GR. Stem cortex CSA (%) and vascular bundle (VB) density (no./mm²) were positively related to stem TMD and negatively related to pupation rate. The GR was positively related to VB CSA (%) and negatively related to VB density. These results suggest that stem TMD, which results from a high fraction in cortex CSA and high VB density, is a key determinant of resistance to a stem‐boring specialist in A. philoxeroides. The high resistance of plants with higher stem TMD may partially impose a cost to plant growth.     

耕作措施对冬小麦田杂草生物多样性及产量的影响

在连续5a秸秆全量还田的免耕、旋耕、耙耕、深松和常规耕作试验地中,设置了除草和不除草处理,研究了其对杂草总密度、优势杂草种类、生物多样性指数和冬小麦产量的影响,并分析了杂草与小麦间的竞争关系。结果表明,麦田杂草主要有7种,分别是麦蒿(Descuminia sophia (L.) Webb ex Prantl)、荠菜(Capsella bursa-pastoris (L.) Medik)、燕麦(Avena sativa L.)、田旋花(Convolvulus arvensis L.)、刺儿菜(Cirsium setosum (Willd.) Bieb.)、繁缕(Stellaria media (L.) Vill.)、麦家公(Lithospermum arvense L.)。在未除草条件下,免耕、深松的杂草总密度显著提高;而在除草条件下,杂草密度显著下降。免耕、深松、常规耕作在未除草条件下,优势杂草种类为麦蒿、荠菜,旋耕、耙耕条件下的优势杂草为麦蒿;而除草后各处理的优势杂草均只有麦蒿。耙耕、常规耕作措施在未除草条件下杂草群落具有较高的物种丰富度和均匀度。无论哪种耕作措施,除草能提高冬小麦产量,其中以深松耕作结合除草处理的小麦产量最高。在小麦抽穗期,未除草处理杂草株高接近或高于小麦株高,会造成杂草与小麦间的光竞争,对小麦的生长状况有显著影响,从而导致小麦产量降低。     

不结球白菜种子活力及抗氧化特性在人工老化过程中的变化

以不结球白菜品种‘寒笑’种子为材料,研究高温(42℃)高湿(相对湿度100%)人工老化处理过程中种子活力及抗氧化相关特性的变化。结果显示:不结球白菜种子的发芽率、发芽势、发芽指数和活力指数随老化处理时间的延长而逐渐下降,不正常苗率逐渐增加;种子的超氧阴离子(O2.-)产生速率先增高后降低,过氧化氢(H2O2)含量逐渐增加,脂氧合酶(LOX)活性和丙二醛(MDA)含量下降,种子浸出液相对电导率增加;种子超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽还原酶(GR)活性随老化处理时间的延长逐渐下降,抗坏血酸过氧化物酶(APX)和谷胱甘肽过氧化物酶(GPX)活性在老化处理初期(老化3 d前)均增加,APX活性随后降低,GPX活性无显著变化;种子抗坏血酸(AsA)和还原型谷胱甘肽(GSH)含量在老化处理1 d后即显著降低并持续保持较低水平。研究表明,不结球白菜种子在人工加速老化过程中其抗氧化系统代谢紊乱并造成活性氧累积伤害,这可能是引起不结球白菜种子老化的重要原因。     

Acute toxicity and adverse effects of aqueous and ethanol extracts of Parkia biglobosa pods on biochemical parameters of Clarias gariepinus

The acute toxicity of the aqueous and ethanol extracts of Parkia biglobosa pods against Clarias gariepinus was investigated under laboratory conditions. Agitated behaviours and respiratory distress were also observed during the exposure period. The adverse effects on biochemical parameters were assessed using semi-static bioassays for 28 days. The ethanol extract of P. biglobosa pods was found to be more acutely toxic with a 96 h LC₅₀ value of 13.96 mg l^?1 than the aqueous extracts, with a 96 h LC₅₀ value of 19.95 mg l^?1 against C. gariepinus. Both extracts induced agitated behaviours and respiratory distress in exposed organisms. The activities of superoxide dismutase (SOD), catalase (CAT) and the concentration of malondialdehyde (MDA) were significantly lower (p < 0.05) in groups of organisms exposed to extracts of P. biglobosa when compared with the control group after 14 days. The activities of aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (ALP) were also significantly (p < 0.05) lower compared with activities of the enzymes in the control group after 28 days. The current study has shown that the introduction of P. biglobosa pods into aquatic ecosystems is acutely toxic to fish and would possibly be to other non-target aquatic organisms especially invertebrates.     

阿帕替尼对人肝癌细胞增殖及凋亡的作用机制研究

目的:探讨阿帕替尼抑制肝癌细胞增殖促进凋亡的作用机制。方法:选取肝癌细胞系SNU739、HepG2,以CCK-8细胞增殖实验、平板克隆实验测定阿帕替尼对肝癌细胞增殖及克隆形成能力的影响;流式细胞术检测阿帕替尼对肝癌细胞凋亡的影响;蛋白免疫印迹法检测阿帕替尼影响肝癌细胞凋亡相关蛋白Bax、Bcl-2及Caspase3的表达情况。结果:与对照组相比,阿帕替尼可显著抑制肝癌细胞增殖(P0.05)。平板克隆实验提示与对照组相比,10μM和20μM阿帕替尼组肝癌细胞克隆数明显减少(P0.05)。流式细胞术结果提示10μM和20μM阿帕替尼处理组细胞凋亡率明显增加(P0.05)。蛋白免疫印迹法结果显示经阿帕替尼处理的肝癌细胞,促凋亡蛋白Bax及Caspase3的活性片段Cleaved-caspase3表达水平显著上调,抗凋亡蛋白Bcl-2显著下调(P0.01)。结论:阿帕替尼通过调节肝癌细胞凋亡相关蛋白从而抑制肝癌细胞增殖、促进其凋亡。     

骨髓间充质干细胞与聚3-羟基丁酸酯-co-4-羟基丁酸酯生物材料共培养细胞补片的初步研究

目的:研究聚3-羟基丁酸酯-co-4-羟基丁酸酯[P(3HB-co-4HB)]这种新型高分子材料与骨髓间充质干细胞(BMSCs)共培养,观察材料对干细胞的存活及增殖的影响,形成细胞补片的效果;从而找到一种适合BMSCs生长、增殖的高分子生物材料,作为治疗心肌梗死,软骨损伤等多种组织损伤疾病的修复方法之一。方法:取清洁级雄性健康BSL-C57小鼠作为实验对象,通过分离培养获得小鼠BMSCs,并进行流式细胞仪鉴定表面标志物。BMSCs培养至5代后,将BMSCs与P(3HB-co-4HB)制成的生物材料薄膜共培养,24h后固定进行电镜扫描,并用DAPI荧光染料染色处理,在荧光显微镜下观察并进行细胞计数,并描绘生长曲线。结果:BMSCs流式细胞术鉴定:CD34、CD45阴性,CD90弱阳性,CD73阳性。扫描电镜下,P(3HB-co-4HB)材料与BMSCs共培养形成的细胞补片,其表面细胞数量多,细胞状态正常。荧光显微镜下,对其细胞补片表面的细胞进行计数,并绘制生长曲线,显示表面细胞有逐渐增多的趋势。结论:P(3HB-co-4HB)材料与BMSCs共培养制成的细胞补片表面有细胞存活及增殖,由于P(3HB-co-4HB)材料本身具有良好的生物组织相容性及可降解等性质,所以该新型高分子材料可以作为干细胞治疗多种疾病的支架材料之一。     

昆虫杆状病毒系统表达口蹄疫病毒3ABC基因

以O型口蹄疫病毒为研究对象,经过RTPCP扩增得到非结构蛋白3ABC基因,克隆到转移载体pFastbacHT,将其转入含穿梭载体Bacmid的DH10Bac,与Bacmid发生位点特异性转座作用,得到3ABC的重组穿梭载体Bacmid3ABC,再将其转染昆虫细胞HiFive。PCR鉴定证实3ABC基因正确地插入到病毒基因组的多角体蛋白基因启动子下游,经过SDSPAGE和Westernblot检测,3ABC基因在昆虫细胞中表达了大小约为50kDa的蛋白条带,3ABC基因在BactoBac系统中的成功表达为建立以基因工程产品为抗原、鉴别诊断自然感染和免疫动物的方法提供了技术条件。