APPLICATION OF HMB－45 MONOCLONAL ANTIBODY AND S100 PROTEIN IN THE IMMUNOHISTOCHEMICAL DIAGNOSIS OF MELANOMA

ＡＰＰＬＩＣＡＴＩＯＮＯＦＨＭＢ－４５ＭＯＮＯＣＬＯＮＡＬＡＮＴＩＢＯＤＹＡＮＤＳ１００ＰＲＯＴＥＩＮＩＮＴＨＥＩＭＭＵＮＯＨＩＳＴＯＣＨＥＭＩＣＡＬＤＩＡＧＮＯＳＩＳＯＦＭＥＬＡＮＯＭＡＬｉｕＤａｎｙａ（刘丹亚）；ＳｕＢａｏｓｈａｎ（苏宝山）；Ｘｕ...     

Projected prevalence of car-sharing in four Asian-Pacific countries in 2030: What the experts think

This paper presents a “big-picture view” for policymakers and related stakeholders regarding the future development of car-sharing services. Car-sharing has the potential to significantly disrupt the personal mobility market. Thus, understanding their market penetration and implications is urgently needed. Previous studies in this domain have predominantly focused on the views, opinions, and preferences of consumers. In this study, we complement the current demand modelling research on car-sharing by applying an expert elicitation and aggregation technique that relies on transport experts’ opinions to investigate the role of car-sharing in the future. Specifically, based on the opinions of mobility suppliers, this research elicits experts’ judgment from across government, industry, and academia to gain insights into the future of car-sharing markets in four countries – Australia, Malaysia, Indonesia, and Thailand. The analysis reveals that, from a mobility supplier’s perspective, energy and vehicle prices will not have a statistically significant impact on the future adoption of car-sharing. The results also show that the more knowledgeable an expert is, the more pessimistic they are about the market penetration of car-sharing in 2016, and the more optimistic they are about the prevalence of car-sharing in 2030.     

幽门螺杆菌尿素通道蛋白基因UreI载体的构建、融合表达及纯化

目的构建幽门螺杆菌(H.pylori,Hp)尿素通道蛋白基因UreI的融合表达载体,并在E.coliBL21中表达,为进一步研究UreI的功能奠定基础。方法利用分子克隆技术以Hp DNA染色体为模板,扩增Hp UreI基因片段,将目的基因UreI与载体pET32a( )分别经kpnⅠ和HindⅢ双酶切,纯化,连接。筛选阳性重组载体,转化大肠杆菌BL21,以IPTG诱导表达pET32a( )/UreI融合蛋白。表达产物经Ni-NTA琼脂糖树脂纯化后,用SDS-PAGE及Western blot分析。结果经酶切、测序分析表明,插入的基因片段为Hp UreI编码基因,由585 bp组成,与GenBank相应菌株HP AM417 609序列完全一致,无碱基突变。经SDS-PAGE分析显示重组质粒pET32a( )/UreI在原核细胞中得到了高效融合表达,其重组融合蛋白分子量为130 ku,经Ni-NTA琼脂糖树脂纯化后,其纯度达95%以上,Western blot分析显示,该重组融合蛋白可被6-His鼠抗单克隆抗体所识别,具有良好的反应原性。结论成功地克隆和构建了原核表达载体pET32a( )/UreI,并在原核细胞中得到了高效融合表达。     

WWOX蛋白在非小细胞肺癌中的表达及其临床意义

目的 探讨WWOX(WW domain-containing oxidoreductase)基因在非小细胞肺癌组织中的表达及其临床意义.方法 用免疫组化方法检测50例鳞癌、31例腺癌及20例癌旁正常组织中WWOX基因蛋白的表达,并分析其与各临床病理指标之间的相关性.结果 WWOX基因在72.8%的非小细胞肺癌中失表达或表达减少,而在相邻正常肺组织中有80.0%正常表达.WWOX基因的表达与组织类型、细胞分化程度密切相关(P<0.05),在鳞癌和低分化癌中WWOX基因失表达或表达减少.结论 WWOX蛋白在非小细胞肺癌组织中呈低表达,该蛋白表达的缺失可能在不同类型非小细胞肺癌的形成中发挥了不同的作用.     

AMP激活的蛋白激酶对大鼠弥漫性轴索损伤后神经元自噬的调节

目的研究AMP激活的蛋白激酶(AMPK)信号通路在弥漫性轴索损伤(DAI)大鼠脑组织中的表达,探讨AMPK对DAI后神经自噬的调节机制。方法大鼠头颅瞬间旋转损伤法建立DAI模型,免疫蛋白印迹法检测造模后1、3、7d大脑皮层和海马AMPK、磷酸化AMPK(p-AMPK)、Beclin1、LC3Ⅰ/Ⅱ、p62蛋白的动态表达,并与正常组和假手术组比较。侧脑室给予AMPK抑制剂Compound C及激活剂AICAR,检测药物干预对大鼠神经自噬相关蛋白表达的影响,并与DAI组和vehicle组进行比较。结果与正常组和假手术组相比,DAI 1d后脑内AMPK信号通路激活,3d后脑内自噬水平上调;Compound C可以减少AMPK磷酸化激活同时下调脑内的自噬水平,AICAR可以增高AMPK磷酸化水平上调神经自噬改善神经功能损伤。结论大鼠DAI后AMPK的激活可以上调神经自噬的水平,对DAI后的神经保护有重要意义。     

急性脑梗死患者血C反应蛋白水平与颈动脉粥样硬化的关系

目的探讨急性脑梗死患者血C反应蛋白(CRP)水平与颈动脉粥样硬化的关系。方法对52例急性脑梗死患者和30例对照组进行观察。采用速率散射比浊法测定血CRP含量;应用美国Acuson Sequoia 521彩色电脑声像仪检测颈动脉内膜-中膜厚度(IMT),观察颈动脉粥样斑块。结果急性脑梗死患者血CRP含量、颈动脉IMT和粥样斑块数较对照组明显增加;血CRP水平与临床神经功能缺损评分、吸烟指数、颈动脉IMT及斑块数呈正相关。结论CRP作为炎性指标可能在促进动脉粥样硬化的发生和发展中起了重要的作用;血CRP水平可作为急性脑梗死患者病情轻重和预后的评价指标。     

内皮素-1诱导大鼠血管平滑肌细胞产生C-反应蛋白的作用

目的观察内皮素-1(ET-1)诱导血管平滑肌细胞(VSMCs)产生C-反应蛋白(CRP)的作用及其机制。方法培养大鼠VSMCs,以不同浓度ET-1刺激VSMCs,并用ETA拮抗剂BQ123、抗氧化剂PDTC、p38MAPK抑制剂SB203580及ETB阻断剂BQ788进行干预,免疫细胞化学法及半定量逆转录聚合酶链反应(RT-PCR)法分别测定不同浓度及不同干预因素下VSMCs中CRP蛋白及mRNA的表达。结果 ET-1能刺激VSMCs CRP蛋白及mRNA的表达增强,其效应呈浓度依赖性;BQ123、PDTC及SB203580能明显减少ET-1诱导的大鼠VSMCs CRP蛋白及mRNA的表达,而BQ788对此作用无明显影响。结论 ET-1通过ETA、活性氧(ROS)、p38MAPK诱导大鼠VSMCs产生CRP。     

孕妇血清铜值与胎盘功能的关系

用火焰原子吸收法测定了孕28～40周正常孕妇83例,孕37～40周重度妊娠高血压综合征及41周以上妊娠妇女42例的血清铜值,并与同期尿E/C比值及新生儿Apgar评分相比较,结果提示:孕妇血清铜值在40周前随孕周的增长而增高。41周以上妊娠,重度妊高征血清铜值偏低。当尿E/C比值<10及Apgar评分≤7分时,孕妇血清铜值低,提示孕晚期母亲血清铜值可作为判断胎盘功能的辅助指标。     

THE QUANTITATIVE MEASUREMENT OF BCL-2, P53 PROTEIN AND PCNA EXPRESSION IN BREAST CARCINOMA AND THEIR CORRELATION WITH PROGNOSIS

Recently,alargenumberofresearchesindicatedthatoccurenceanddevelopmentofbreastcarcinomaswerecorrelatedwithhighexpressionofblockingapoptosisoncogene,mutationofantioncogeneandexpressionofcontrollingcellproliferativeoncogene.Therewerefewreportsondocumentsofquantitativestudyofexpressionaboutblockingapoptosisoncogene--hcf--2(Bcellleukaemia/lymphomagene),productofP53proteinandproliferatingcellnuclearantigen(PCNA)inbreastcarcinoma.Ourpurposewastoinvestigatequantitativeindexinrelationtoclinicalpathol…