miR-106b-5p靶向KLF4调控山羊肌内前体脂肪细胞分化

旨在明确miR-106b-5p对山羊肌内前体脂肪细胞分化的影响，并确定这种作用是通过靶向KLF4来实现的。本研究利用实时荧光定量PCR （quantitative real-time PCR，qRT-PCR）技术检测miR-106b-5p在山羊肌内前体脂肪细胞分化过程中的表达模式，通过脂质体转染技术将miR-106b-5p mimic和miR-106b-5p inhibitor转入体外培养的山羊肌内前体脂肪细胞，油红O染色法从形态学验证miR-106b-5p对脂肪细胞中脂滴积聚的影响，qRT-PCR检测预测的靶标基因KLF4和脂肪分化标志基因的表达情况，利用双荧光素酶报告系统鉴定miR-106b-5p与KLF4的靶标关系。qRT-PCR结果显示，miR-106b-5p在山羊肌内前体脂肪细胞诱导分化第3天时表达量最高。在山羊肌内脂肪细胞中干扰miR-106b-5p后油红O染色显示脂滴聚积减少，过表达miR-106b-5p后脂滴聚积增加。在山羊肌内前体脂肪细胞中转染miR-106b-5p inhibitor后PPARγ表达量显著降低（P<0.05），而KLF4表达量极显著升高（P<0.01）；转染miR-106b-5p mimic后LPL和PPARγ表达量极显著升高（P<0.01）。荧光素酶活性试验结果显示，过表达miR-106b-5p可显著抑制KLF4荧光活性。miR-106b-5p通过靶向并负调节KLF4的表达促进山羊肌内脂肪细胞分化。     

都市田园，时代更迭下的绿色传承——访农耕田缘生态园区总经理王海宝

已是冬月,广州市从化区西塘镇依旧温暖如春,生机盎然。走进农耕田缘生态园区(以下简称农耕田缘),颇有一种“久在樊笼里,复得返自然”的自由之感。人们身着薄衫,撑着阳伞,行走于石径小路之上,周边亭台轩榭,绿草如茵,菜花争奇斗艳,鸡鸭成群结对,空气中飘散着蔬果淡淡的清甜,令人重拾田园归去的悠然与欢愉。在这片隔绝了城市喧嚣与生活繁琐的地域里,农耕田缘以健康为旨、自然为根、良心为翼、科技为锄,搭建起鸡菜共生、鸭稻共作的生态共享模式。由此,西塘镇开启绿色有机的农业生态之旅,与当地村民携手迈入增收致富的康庄大道。     

河北省小麦机械化生产发展现状及对策

河北省是我国小麦主产区以及优质小麦主产区,目前已基本实现全程机械化作业,该地区小麦生产的稳定与可持续对粮食安全战略具有积极影响。通过对河北省小麦机械化生产现状梳理与分析,结合全省小麦生产实际情况,提出该地区小麦生产农机装备的发展方向为"节水、复式、高效、绿色"。     

白蛾黑基啮小蜂种群数量变化规律的初步研究

选择徐州市林果场、云龙区和新沂市等受杨小舟蛾危害较重的不同类型杨树林分的未放蜂区(CK)和放蜂区,分别测定白蛾黑基啮小蜂在自然和人工释放2种状态下的种群数量变化。结果表明,该蜂林间自然种群数量以越冬代最高,对杨小舟蛾越冬蛹的寄生率高达(22.2±5.8)%,极显著高于第1~4代蛹(3.4%~6.4%);于越冬代和第2代害虫蛹期人工释放该蜂,释放后当代小蜂种群数量明显上升,可显著提高释放当代(越冬代和第2代)害虫蛹的寄生率,并对释放后各代害虫蛹具有一定的持续寄生效果;各代小蜂室温下的羽化进度均与相应世代寄主蛹发育进度相吻合。     

塞罕坝湿地资源现状与保护对策

文章阐述了塞罕坝湿地资源现状调查方法,并以调查资料为依据,以湿地类型、野生动植物资源状况为主要内容,分析了塞罕坝湿地资源现状和基本特征,并结合湿地所处社会环境等,提出了塞罕坝湿地的保护对策,为塞罕坝湿地保护与恢复提供基础支撑。     

基于blackboard教学平台的嵌入式信息素质教育发展策略

blackboard教学平台与嵌入式信息素质教育的结合,对图书馆员、教师和学生都具有非常重大的影响。本文通过对国外blackboard应用的现状和国内高校应用blackboard的可行性进行分析,总结出高校借助Blackboard教学平台开展嵌入式信息素质教育的发展策略。     

Effect of AIR on Inflammatory Reaction Infected by Brucella

In order to investigate the effect of AIR on inflammatory reaction infected by Brucellamelitensis (16M), the AIR domain of Tecpr1 gene of murine macrophages RAW264.7 were knocked down (I-A), overexpressed (O-A) and reversed (OA-IA). Using the chlorine fluorescein (DCFH-DA) as a probe, we detected the variation of ROS production and mitochondria distribution by confocal laser scanning microscopy. We observed the expression changes of NLRP3, ASC and Caspase-1 by qRT-PCR and the expression changes of IL-18,IL-1β and Caspase-1 in host cells by ELISA. The results showed that 16M could stimulate RAW264.7 cells to produce ROS by time-dependent pathway, and I-A group and O-A group showed more abnormal accumulation of mitochondrial. The results of qRT-PCR and ELISA suggested that it had effect on the expression levels of NLRP3, ASC,Caspase-1 and IL-18, IL-1β and Caspase-1 in cells of different groups. Those results indicated that with AIR gene deletion, the release amount of ROS changed, mitochondrial clustered abnormally, and AIR was closely related to the activation of inflammasomes and induction of inflammatory reactions.     

Advances on Detection Methods for Residues of Nitrofurans in Food

Nitrofurans are broad-spectrum antibiotics which have been widely used in food animals to the prevention and treatment of gastrointestinal infections.Due to abuse of drugs by criminals,animals could produce drug-resistant strains,which reduces the role of antibiotics.Meanwhile,excessive drugs residues in food has carcinogenic,teratogenic and mutagenic effects to the human body.In this paper,the damage and the detection methods of the residues of the nitrofurans in food are surveyed.The main detection methods include high performance liquid chromatography,liquid chromatography-mass spectrometry,liquid chromatography tandem mass spectrometry,enzyme-linked immunoassay,colloidal gold immunoassay and fluorescence immunity analysis method.The research status of various detection methods are summarized and the suggestions for further research are put forward.It is expected to provide reference for future research.     

芒果核仁油理化特性及其开发利用研究进展

芒果核仁是芒果加工的副产物,其中脂肪含量达9.0%~13.1%（干基）,从中提取的核仁油是一种优质油脂,具有较高的营养价值及开发利用前景。本文主要从芒果核仁油理化性质、脂质组成及开发利用等方面总结归纳近年来的科学研究进展,并与可可脂、类可可脂的甘油三酯组分进行对比分析,明确了芒果核仁油研究中存在的问题,并给出合理建议。     

表达鸡α干扰素重组酿酒酵母菌的构建与鉴定

通过构建鸡α干扰素真核表达载体,以获得能够表达鸡α干扰素的酵母工程菌株。首先根据GenBank公布的鸡α干扰素基因序列设计上、下游引物,以略阳乌鸡基因组DNA为模板,PCR扩增鸡α干扰素基因片段。然后,利用基因重组技术将鸡α-干扰素基因插入真核表达载体,通过菌落PCR和DNA测序确定目标载体,构建成功后转化至酿酒酵母AH109,再通过营养缺陷培养、质粒提取和PCR鉴定带JMB440-ChIFN-α载体的重组酵母菌株。最终通过酵母培养、总蛋白收集、SDS-PAGE电泳和Western blot等,确定鸡α干扰素基因能够与酵母菌株重组,并表达α干扰素,蛋白条带大小约为23ku,与预期结果一致,表明成功构建了表达鸡干扰素基因的工程酵母菌株。