轻型木结构建筑覆板的集中静载性能

介绍轻型木结构建筑覆板集中静载结构性能试验的装置、条件和方法,并进行国产人工林落叶松胶合板作轻型木结构覆板的集中静载性能研究.结果表明:与国外胶合板覆板具有相同厚度的国产落叶松屋面板和楼面板,其集中载荷性能均优于相关标准的要求.     

造林新材料在岱山海岛造林中的应用

通过3种造林新材料在岱山海岛造林中的应用,观测它们对提高造林成活率的影响.结果表明:3种造林新材料对提高夹竹桃Nerium indicum造林成活率基本没有影响,科瀚98对枫香Liquidambar formosana和银杏Ginkgo biloba造林成活率影响较小.植树宝、科瀚98和GGR可显著提高女贞Ligustrum lucidum,重阳木Bischofia javanica,香樟Cinnamomum camphora和木荷Schima superba的造林成活率.图1表1参6     

表面技术在内燃机气缸套中的新进展

论述了气缸套的失效机理，针对这一缺点，较全面地阐述了当前表面技术在气缸套上的应用现状，并提出了未来气缸套的发展方向。为同行提供了参考和启迪，也为拓宽热喷涂技术的应用指明了一个方向。     

基于图形旋转系统的渐进网格研究

拓扑简化可以为渐进网格带来更好的效果，但目前几乎所有的渐进网格方法都不支持拓扑简化，而且edge collapse和vertex split操作有时会产生非流形．针对这些问题，提出了基于图形旋转系统的渐进网格法．以基于图形旋转系统的数据结构和操作实现了渐进网格，用图形旋转系统的操作集合构建了edge collapse和vertex split操作．在此基础上，通过扩展新操作即可进行任意拓扑变化，从而实现拓扑简化，     

Antisense drug targeting with VEGF mRNA designed by computer aid and inhibitory effects on K562 cell line in vitro

AIM:The effective antisense sequences targeted VEGF mRNA with computer software would be screened and designed, and effect of them on growth K562 cells and protein expression of VEGF were studied with experiments.METHODS:Seven antisense sequences were selected and synthesized, which consisted of 18-20 deoxynucleotide acid and were modified with phosphorothioate, according to principle of low free energy of overall △G₃₇ Overall. Cell growth was assayed by trypan blue dye exclusion assay and level of VEGF protien in the media was determined by ELISA.RESULTS:Six of seven sequences were capable of inhibing growth of K562 cells and downregulating the VEGF protein expression significantly, compared with Scrambed control group. It was found that there was a close correlation between low level of overall △G₃₇ and antisense effectiveness (r=0.887,P<0.01).CONCLUSION:VEGF mRNA antisense oliogdeoxynucleotides, which were designed by computer software of RNAstructure, were able to inhibit growth of K562 and its protein expression. The VEGF mRNA may be new target attached by drugs. At same time, the computer aided design is useful methods to obtain the effective antisense.     

热胁迫对辣椒花柱细胞中Ca2+ 分布的影响

 用焦锑酸钾沉淀法研究了热胁迫对辣椒开花前后柱头和花柱细胞中Ca²⁺分布的影响。结果表明: 常温下Ca²⁺ 分布在柱头细胞表面、花柱引导组织细胞间隙等质外体系统中, 且在花粉管上呈先增加后减少的规律性变化; 热胁迫后, 除细胞间隙等质外体系统外, 细胞质和细胞核中也出现Ca²⁺, 花柱引导组织中通过的花粉管发生扭曲、变形, 这可能与Ca²⁺ 的异常分布有关。     

重组鸡IL-2增强鸡四联灭活苗免疫效果的研究

使用在原核表达系统中表达的重组鸡白细胞介素 2 (IL 2 )蛋白 ,经过初步的分离纯化 ,与鸡新城疫 禽流感 法氏囊 传染性支气管炎四联油乳剂灭活苗同时使用 ,检测其对疫苗的免疫增强效果。试验共分 5组 ,每组 1 0只鸡。其中对照组只注射四联油乳剂灭活苗 ;4个试验组 ,在注射疫苗的同时分别注射重组鸡IL 2蛋白 0 0 5mg、 0 0 1mg、 0 1 5mg、 0 2 0mg。试验组与对照组同时各注射新城疫等多联油苗 0 5mL。采用HA、HI试验测定鸡新城疫、禽流感抗体滴度。结果表明 :重组鸡IL 2对该四联油乳剂灭活苗有较强的免疫增强作用。以第 3、 4组的增强效果较为明显 ,其中对鸡新城疫病毒和禽流感抗原的抗体效价 ,与对照组相比分别提高 2 42 8和 2 2 3 0个滴度。重组鸡IL 2在使用的过程中 ,没有发现任何毒副作用 ,证明是一种安全高效的免疫增强剂。     

Expression of cyclooxygenase-2 in IL-1β-stimulated mesangial cells is medicated by NF-κB/IκB signal pathway

AIM: To investigate the role of NF-κB/IκB signal pathway in the regulation of cyclooxygenase-2 (COX-2) expression in human mesangial cells (HMC). METHODS: The PGE₂ concentration in supernatants of HMC was measured by radioimmunoassay. COX-2 mRNA and protein expression were determined by RT-PCR and Western blot. Electrophoretic mobility shift assay (EMSA) and Western blot were used to detect the activity of NF-κB and degradation of IκB. RESULTS: IL-1β significantly upregulated COX-2 expression and PGE₂ production in HMC. Significant up-regulation of NF-κB activation, nuclear translocation of p65 subunit, and degradation of IκB α and IκB β were observed in IL-1β-induced HMC. CONCLUSION: Expression of COX-2 in IL-1β-induced HMC is mediated by NF-κB/IκB signal pathway.     

Inhibition of K562 cell growth by antisense drug targeting with VEGF mRNA in vitro

AIM: To investigate inhibition of K562 cell growth by antisense drug targeted VEGF mRNA. METHODS: X7, 20-mer antisense sequences were selected, synthesized and modified with phosphorothioate. The drug was transfected into K562 cells in the present of lipofection. Cell growth was assayed by trypan blue dye exclusion assay and MTT. The level of VEGF protein in the media was determined by ELISA. The morphology of apoptotic cells were observed by Giemsa staining, and the propotion of apoptotic cells was detected by flow cytometry. RESULTS: The antisense drug inhibited growth of K562 and downregulated expression of VEGF protein significantly, compared with Scrambed control group and showed dose-dependent relation. Signs of apoptosis of K562 cells were not observed. CONCLUSION: Inhibition of K562 cell proliferation, but not cells apoptosis induction is the mechanism of inhibing growth of K562 cells by antisense drug targeted VEGF mRNA. At same time, VEGF has function of promoting K562 cell proliferation, and VEGF mRNA may be a new target attached by drugs.