基于数据挖掘分析何泽云教授治疗CKD的用药规律

目的 基于数据挖掘方法分析何泽云教授治疗慢性肾脏疾病（chronic kidney disease，CKD）的用药规律。方法 收集何泽云教授治疗CKD病例336份，处方1 110张，采用SPSS 17.0及数据挖掘软件clementine 12.0分别对处方进行频次分析和关联规则分析。结果 单味药使用频次由高到低依次是白茅根、山药、黄精、熟地黄、黄芪，使用频率最高的类别是补益类药物（总频率达49.6%）；关联规则分析结果显示，支持度较高的药对依次为白茅根-山药、白茅根-麦冬、白茅根-黄精、白茅根-熟地黄、白茅根-黄芪、山药-黄精、山药-熟地黄。结论 何泽云教授以培元固本，健脾补肾为基本治疗大法，辅以固精、滋阴、泄浊之法论治CKD，数据挖掘方法对于中医临床经验总结具有重要实用价值，为中医治疗CKD用药筛选及中药研发提供思路。     

花生种子特异启动子AHSSP1的克隆及功能分析

为丰富花生种子特异启动子资源,本研究利用PCR技术在花生基因组中克隆了种子贮藏蛋白基因PSC32的启动子AHSSP1,利用半定量RT-PCR检测了PSC32基因表达模式,借助NewPLACE在线分析了AHSSP1序列中存在的顺式作用元件,并构建了AHSSP1驱动GUS报告基因的表达载体,经农杆菌转化获得转基因拟南芥,经GUS组织化学染色鉴定了该启动子的功能。结果表明,PSC32基因957 bp长的启动子AHSSP1序列具备种子特异表达启动子特有的3个RY REPEAT元件。半定量RT-PCR分析发现,PSC32基因在花生成熟种子中表达,而在饱果成熟期根、茎、叶片、花、入土前的果针、成熟种子的果壳中均不表达。GUS组织化学染色发现,转基因拟南芥成熟种子以及萌发种子的子叶、下胚轴和胚根均能够被染上蓝色;长出真叶后,子叶和下胚轴仍能被染色,而根和真叶不能被染上蓝色;成年期转基因拟南芥的叶片也不能被染上蓝色。而野生型拟南芥整个生长时期均不能被染上蓝色。以上现象说明AHSSP1是一个种子特异启动子。本研究丰富了花生种子特异启动子的资源,对花生籽仁品质改良或以花生籽仁作为“生物反应器”的研究具有重要的应用价值。     

松材线虫纤维素酶的免疫学分析

制备松材线虫特定纤维素酶的多克隆抗体(Anti-BXC60),通过SDS-PAGE、纤维索酶酶染分析、免疫印迹以及ELISA方法考察该抗血清的特异性.进一步利用抗松材线虫全蛋白抗体(Anti-BX)和Anti-BXC60抗体,建立线虫分泌性蛋白在PVDF膜上双重染色的方法.双重染色分析的结果表明:松材线虫主要通过分泌孔向体外分泌大量的分泌蛋白,而纤维素酶的分泌方式与其他植物线虫相似,是通过口针向外分泌.     

Proteins in Norway spruce thermomechanical pulp

Two methods of cytochemical staining using Coomassie dye and Cu⁺-bicinchoninic acid, respectively, showed that there are proteins in thermomechanical pulp (TMP) of Norway spruce. Protein isolated from TMP was analyzed for amino acid composition. There was about twice the amount of acidic amino acid material compared with basic amino acids, and the presence of glucosamine indicated that the isolated polypeptides also contained glycoproteins. The presence of proteins in ray cells and fiber tracheids in TMP adds to the chemical heterogeneity of the structurally complex high-yield pulp.     

Development of cell model of polymer/liquid crystal and effect of their elasticity on adhesion of rBM-MSCs

AIM: To develop the cell model of polymer/liquid crystal and to study the effect of their elasticity on the adhesion of rat bone marrow mesenchymal stem cells (rBM-MSCs). METHODS: Using the method of solvent evaporation induced phase separation, the cell model of polymer/liquid crystal was constructed. The surface morphology and phase separation structure were determined by polarized optical microscopy (POM), scanning electron microscopy (SEM) and small angle X-ray scattering (SAXS). rBM-MSCs were separated and expanded by adherent culture. The surface markers of rBM-MSCs were detected by flow cytometry. The cells were induced to osteogenic differentiation and adipogenic differentiation for 2 weeks. After 3 passages, the cells were divided into 4 groups, including total PU control group, 10% membrane group, 30% membrane group and 50% membrane group. The cells were then incubated with rhodamine phalloidin for cytoskeleton staining and were observed under the confocal laser scanning microscope after cultured for 24 h. RESULTS: The cell model of polymer/liquid crystal was constructed successfully using the method of solvent evaporation induced phase separation. Flow cytometry results showed that the rBM-MSCs positively expressed CD29, CD44 and CD90, and negatively expressed CD34 and CD45. After stained with alizarin red S and oil red O, the calcium nodule and lipid droplets in rBM-MSCs were observed obviously. The cytoskeleton staining result indicated that the area in total PU control group, 10% membrane group and 30% membrane group were greater, and the actin microfilaments were also clearer than that in 50% membrane group. CONCLUSION: The cell model with suitable content of liquid crystal made a contribution to the rBM-MSCs' adhesion, but too much liquid crystal inhibits cell adhesion.     

A rapid differential staining technique for Fusarium pseudograminearum in cereal tissues during crown rot infections

A novel fluorescence‐based differential staining procedure has been developed for the rapid visualization of Fusarium pseudograminearum hyphae in cereal tissues. Infected tissues are stained with safranin, which binds to host cell walls, while hyphal tissues are stained with the fluorescent dye solophenyl flavine 7GFE. The method is rapid, does not require clearing of culm cross‐sections, and provides high contrast informative images of fungal and plant structures during pathogenesis.     

The effect of feeding commercial diets on the development of juvenile crucian carp (Carassius carassius,L.). Part 1: Skeletal deformations

The crucian carp (Carassius carassius, L.) is a cyprinid freshwater species, whose wild‐living populations have decreased in recent years due to an increasing competition of invasive species. Several initiatives were launched, attempting to reintroduce this fish back into its native open waters, which requires the use of crucian carp fry grown under controlled conditions. However, the use of popular commercial diets results in severe developmental abnormalities. The aim of this study was to analyse the impact of feeding natural feed (Chironomidae sp. larvae) or two popular commercial diets on the skeletal development of crucian carp juveniles. Whole‐mount staining and histological methods were used in the study. Skeletal tissues of fish fed both commercial diets were demineralized and displayed a variety of deformities, such as abnormal vertebral spines and vertebral fusion, as well as a new type of deformation, which involved the action of dorsal fin pterygiophores upon the spine. Finally, a novel analytical method was proposed, which utilizes LA‐ICP‐MS for the estimation of bone mineralization. The study proved that basic commercial diets are inadequate for the rearing of crucian carp juveniles.     

黑褐新糠虾血细胞形态及其与日本新糠虾对溶藻弧菌敏感性的比较

实验采用Giemsa与Wright' s两种染色方法对黑褐新糠虾血细胞进行染色,根据血细胞大小,所含颗粒与否,颗粒多少和核质比将其分型,并对各型血细胞所占比例进行统计.结果表明,通过比较Giemsa染色与Wright's染色两种方法的染色时间和效果,Wright's染色更加适合糠虾血细胞.通过染色,将黑褐新糠虾血细胞分为3种类型,它们分别为透明细胞、半颗粒细胞和颗粒细胞.它们的胞体大小依次增大,核质比依次降低.对此3种类型血细胞比例分别统计后发现,颗粒细胞所占比例最多约( 48.38％±0.05％),其次是半颗粒细胞约为(35.22％±0.04％),最少的为透明细胞约为(16.40％±0.01％).对不同浓度溶藻弧菌的感染试验发现,日本新糠虾在较短的时间内出现死亡,即48h,而黑褐新糠虾72 h出现死亡,各浓度组中日本新糠虾死亡率均高于黑褐新糠虾.黑褐新糠虾相对日本新糠虾来说,对溶藻弧菌具有较低的敏感性,可能与其血细胞中颗粒和半颗粒比例较高有关.     

VEGF在绵羊生殖管道中的表达规律

以不同发情周期雌性绵羊子宫、输卵管为研究对象,采用免疫组织化学技术,针对血管内皮生长因子（VEGF）在绵羊子宫、输卵管的表达、定位和变化规律进行了检测,同时应用相关图像分析软件对抗原染色强度进行了定量分析。结果表明：输卵管在发情0～15d,VEGF表达量在第9天达到峰值后经历波动逐渐下降过程,输卵管内膜上皮细胞是VEGF抗原的主要靶细胞;而子宫角在发情0～15d,VEGF表达量在第5天达到峰值后经历波动逐渐下降过程,子宫内膜固有层及腺体周围细胞为VEGF抗原的主要靶细胞。该研究结果为绵羊生产中进一步提高受胎率和妊娠率及频密产羔等技术的应用提供了科学依据。     

青蒿非分泌型腺毛特异TPS7基因启动子的克隆及功能分析

研究运用基因组步移法克隆了长度为1 167bp的青蒿启动子proTPS7,经生物信息学分析发现了proTPS7中的多个顺式调控元件。构建启动子与GUS融合载体,稳定转化青蒿并对转基因植株进行GUS染色实验,结果表明该启动子能驱动报告基因在非分泌型腺毛中的特异表达。对转基因青蒿喷洒甲基茉莉酸和脱落酸,3h后GUS基因表达水平有所上调,说明proTPS7能受到上述2种激素的诱导。