FGF4在肺癌细胞体内和体外中表达差异的研究

FGF4已经被证明是癌基因,它涉及肿瘤的生长和转移,为了解FGF4的表达与肿瘤微环境的关系。我们利用FGF4抗体通过免疫组化对一名肺癌患者癌旁,癌组织,癌组织小鼠移植瘤,二次移植瘤以及原代培养的细胞爬片进行FGF4检测,探究其表达差异。通过对比癌组织与对照组（癌旁组织）,FGF4在癌巢中高表达;同样,移植瘤与二次移植瘤的癌巢中与癌旁组织比较,FGF4表达相对较高;但是将癌组织进行原代培养后,免疫组化检测细胞爬片FGF4,发现仅有5%±0.21%的肿瘤细胞表达FGF4,对照蛋白Cytokine作为肿瘤标记物,则在100%的肿瘤细胞中表达。研究提示免疫组化检测到FGF4在体内和体外表达不同,提示肿瘤细胞FGF4的表达与肿瘤微环境调控密切相关,肿瘤微环境对肿瘤细胞的FGF4的调控有着重要作用。     

湖南省R&D投入产出效率研究

以湖南省R&D投入产出活动为研究对象，采用数据包络分析法(DEA)的BCC模型，结合全国30个省市R&D投入产出数据，对2013年湖南省R&D投入产出效率进行比较分析，并根据实证结果提出相关对策及建议.     

木本园林植物对土壤重金属的富集及修复效应研究进展

我国城市土壤重金属污染形势严峻,已经严重威胁到人类健康,因此受到普遍关注.木本园林植物是城市绿化、建设的主体,是城市生态系统中富有生命力的单元.植物能绿化、美化环境但不会进入食物链,可以对重金属污染土壤进行持续修复,已成为城市土壤污染植物修复的重要研究领域.该研究综述了近年来用于重金属污染土壤修复的木本园林植物,对其修复土壤的强化措施进行了探讨.重点阐述了木本园林植物对各种重金属的富集效应,对其耐受性和净化土壤重金属污染的应用潜力进行了分析,并对未来的发展方向进行了展望.     

Regulatory effect of salicylic acid and methyl jasmonate supplementation on ergosterol production in Hericium erinaceus mycelia

We evaluated the biomass and ergosterol content of Hericium erinaceus mycelium, and extracellular enzyme activities in H. erinaceus liquid culture following salicylic acid(SA) and methyl jasmonic acid(Me JA)supplementation. The optimal SA concentration was100 lmoláL-1, where the highest ergosterol content of 2.33 mgág-1was obtained following 6-day cultivation with100 lmoláL-1SA supplementation, and which was significantly higher than the unsupplemented control(p \ 0.01). Following 4-day supplementation with50 lmoláL-1Me JA, the highest ergosterol content obtained was 1.988 mgág-1, which was 25.8 % higher than the unsupplemented control. Our data indicate that SA and Me JA supplementation improves ergosterol content in H.erinaceus mycelium.     

金中都公园的园林景观与历史文化展示

本文试以北京金中都公园设计和建设过程为例,论述如何将园林景观与历史文化的合理展示相结合。提出设计师的创作和实践应该与建设过程相配合,以匠人精神应对施工阶段的现场完形和设计提升。总结了设计项目从概念规划直至建成,设计师的全过程设计的重要性和必要性。探讨了景观与艺术专业的协同设计在文化表达和景观展示中的叠加效应。提出设计师对场地的挖掘和设计推敲,应该随着项目的施工建设进度并以现场设计为核心,并举例论述了现场调整对提升设计品质的重要作用。以期为公园改造和园林景观设计师的工作实践提供有益的参考和引导。     

双波长HPLC同时测定氮沉降处理下杜仲皮和叶中的5种成分

建立双波长高效液相色谱法(HPLC)同时测定模拟氮沉降处理下杜仲Eucommia uimoides皮和叶中松脂醇二葡萄糖苷、桃叶珊瑚苷、绿原酸、京尼平苷酸和京尼平苷等5种活性成分含量的方法。采用Agilent ZORBAX SB-C18柱(250.0 mm×4.6 mm,5μm),以乙腈(A)-2.0 g·kg-1磷酸水溶液(B)进行梯度洗脱(0~12 min,10%A;12~25 min,13%A;25~50 min,30%A;50~65 min,60%A);流速为0.8 m L·min-1;检测波长203 nm,240 nm;柱温30℃。结果表明:松脂醇二葡萄糖苷、桃叶珊瑚苷、绿原酸、京尼平苷酸、京尼平苷等在各自的线性范围内与其峰面积积分值呈良好的线性关系。整个实验期间,杜仲皮和叶中5种成分含量对施氮处理产生了不同的响应,且随季节在变动。该方法能准确、快速地对杜仲皮和叶中多种有效成分同时进行测定,可较好反映浙江高氮沉降区特色名贵药材杜仲皮和叶中多种有效成分的变化。     

漳州市加快发展对台农业交流合作政策选择的研究

随着ECFA的实施,漳台(漳州市、台湾省,下同)农业资源将进一步得到合理配置,漳台农业交流合作的空间和领域将得到更大的拓展。漳州市如何在现有的基础和成效上抓住这些有利时机,突破制约漳台农业进一步合作的瓶颈,努力促进漳台农业合作实现跨越式发展,具有重大的现实意义和深远的历史意义。     

温室黄瓜新品种中农33号的选育

中农33号是以自交系09676和12173为父母本配制的黄瓜一代杂种。植株生长势强,耐低温弱光性好。果实商品性好,颜色深绿、有光泽,腰瓜长约35 cm,瓜粗3.4 cm左右,瓜把长约4.5 cm,心腔较小,果肉为淡绿色。白刺、密,瘤小,无棱。高抗WMV,中抗CGMMV、枯萎病、黑星病。早熟性好,持续结果及丰产优势明显。温室长季节栽培每667 m~2产量高达10 000 kg以上。适宜日光温室和春棚栽培。     

银翘复方药渣发酵处理试栽毛头鬼伞及主要药物成分分析

为回收利用生产银翘片废弃药渣,以毛头鬼伞为供试菌株,发酵处理银翘药渣;建堆配料设计原则为控制总料C/N接近40∶1,以玉米芯为主料(配合添加奶牛粪、尿素),逐渐增大银翘药渣用量,以替代玉米芯;堆料共采用4个配方,配方A(CK):玉米芯200kg,牛粪100kg,尿素3.5kg,辅料6%(生石灰2%、石膏2%、过磷酸钙2%);配方B:玉米芯100kg,银翘药渣50kg,牛粪50kg,尿素1.0kg,辅料6%;配方C:玉米芯75kg,银翘药渣100kg,牛粪50kg,辅料6%;配方D:玉米芯50kg,银翘药渣150kg,牛粪50kg,辅料6%。4个配方堆料总干质量均在200kg以上,依墙建堆成半圆锥形(h≥1.0m,r≥1.4m);发酵升温14d(4-3-3-2-2)、经4次翻堆后,摊料降温装袋接种,待菌丝满袋后脱袋覆土出菇。结果表明:以配方C的产出率为最高,其相应生产指标为,初始C/N为41.66、终点C/N为23.71、腐熟度T为0.569、接种满袋率93.7%、菌袋平均产量381.9g·kg~(-1)、生物学效率41.0%。经HPLC检测,配方C发酵料中绿原酸、牛蒡苷含量分别为5.20~5.40、4.49~5.30μg·g~(-1),其栽培所得子实体中绿原酸、牛蒡苷含量分别为0.40~0.45、3.81~4.27μg·g~(-1),其中牛蒡苷从栽培料到子实体的迁移率达84.93%。     

Mycoplasma pneumoniae induces IL-1β production through activating NLRP3 inflammasome by ROS in RAW264.7 cells

AIM: To investigate whether Mycoplasma pneumoniae (Mp)-induced interleukin-1β (IL-1β) production in RAW264.7 cells is through the activation of NLRP3 inflammasome via reactive oxygen species (ROS). ME-THODS: RAW264.7 cells were randomly divided into 3 groups. In normal group, RAW264.7 cells were treated without Mp. In model group, RAW264.7 cells were treated with 1∶ 10 multiplicity of infection (MOI) of Mp. In NAC group, RAW264.7 cells were pretreated with N- acetylcysteine (NAC) at a concentration of 5 mmol/L for 30 min before infection with Mp. The RAW264.7cells were infected with Mp (1∶ 10 MOI) for 4, 8, 16 and 24 h in model group and NAC group, respectively. The intracellular ROS level was analyzed by flow cytometry. The mRNA expressions of NLRP3, ASC and caspase-1 were detected by real-time PCR. The protein levels of NLRP3, ASC and caspase-1 p20 were determined by Western blot. The levels of pro-inflammatory cytokine IL-1β in the supernatant were measured by ELISA. RESULTS: Compared with normal group, the production of ROS were significantly increased at 4, 8, 16 and 24 h after infection, the mRNA expression of NLRP3, ASC and caspase-1 were increased at 8, 16 and 24 h after infection, the protein levels of NLRP3, ASC and caspase-1 p20 were increased at 16 and 24 h after infection, and the releases of IL-1β were increased at 24 h after infection in model group (P<0.01). Compared with the model group, the level of ROS in NAC group decreased, so as the expression of NLRP3, ASC and caspase-1 at mRNA and protein levels and the releases of IL-1β in the supernatant at the corresponding time points. CONCLUSION: Mp may stimulate the ROS production to activate NLRP3 inflammasome in RAW264.7 cells.