球形压头的滑动速度对材料微米划痕响应的影响

在恒定的法向载荷下,使用Rockwell C 120°金刚石压头对聚碳酸酯(PC)、熔融石英、紫铜和镁合金AZ31进行微米划痕测试,研究滑动速度对试样划痕响应的影响.压入深度小于压头的球锥转变深度,确保仅有压头顶端的圆球部分与试样接触.结果表明:随着滑动速度的增加,压入深度、残余深度和划痕沟槽的宽度均非线性减小,划痕硬度和弹性恢复率均非线性增大;PC和紫铜的划痕摩擦系数先增大后减小,PC的黏弹性行为对其摩擦响应有显著影响;熔融石英的划痕摩擦系数先增大后减小,最后趋于稳定;镁合金AZ31的划痕摩擦系数先减小后增大.熔融石英、紫铜和镁合金AZ31的划痕摩擦系数的变化趋势可通过几何接触模型进行解释.     

Microsatellite instability in gastric cancer: molecular bases,clinical perspectives,and new treatment approaches

Gastric cancer is one of the most aggressive malignancies, with limited treatment options in both locally advanced and metastatic setting, resulting in poor prognosis. Based on genomic characterization, stomach tumour has recently been described as a heterogeneous disease composed by different subtypes, each of them with peculiar molecular aspects and specific clinical behaviour. With an incidence of 22% among all western gastric tumour cases, stomach cancer with microsatellite instability was identified as one of these subgroups. Retrospective studies and limited prospective trials reported differences between gastric cancers with microsatellite stability and those with instability, mainly concerning clinical and pathological features, but also in regard to immunological microenvironment, correlation with prognostic value, and responses to treatment. In particular, gastric cancer with microsatellite instability constitutes a small but relevant subgroup associated with older age, female sex, distal stomach location, and lower number of lymph-node metastases. Emerging data attribute to microsatellite instability status a favourable prognostic meaning, whereas the poor outcomes reported after perioperative chemotherapy administration suggest a detrimental role of cytotoxic drugs in this gastric cancer subgroup. The strong immunogenicity and the widespread expression of immune-checkpoint ligands make microsatellite instability subtype more vulnerable to immunotherapeutic approach, e.g., with anti-PD-L1 and anti-CTLA4 antibodies. Since gastric cancer with microsatellite instability shows specific features and clinical behaviour not overlapping with microsatellite stable disease, microsatellite instability test might be suitable for inclusion in a diagnostic setting for all tumour stages to guarantee the most targeted and effective treatment to every patient.     

基于弦振动测量金属细线的线密度

提出了一种测量金属细线线密度的新方法,并对测量原理、公式进行了较为详细的推导,将测量结果与标准值进行了比较.从测量结果可知,其相对误差较小,说明利用该方法测量细线的线密度确实可行.     

CSS代码命名规则与技巧探讨

合理、科学地对CSS代码命名,能够精简CSS代码,提高代码的开发效率,方便网站设计师对网站进行维护与修改.通过对CSS代码命名规则分析,提出了进行语义化命名、结构化命名和惯例命名三种CSS代码命名技巧.     

土壤肥料学实验课程的教学改革与实践

为全面培育卓越农林人才，提高教学培养质量，本研究结合土壤肥料学的课程内容、教学特点及实验方法，对存在的问题进行了剖析，并结合实际针对存在问题做出了相应改革，适时调整《土壤肥料学》实验课程内容和形式。通过删减验证性实验内容，增设综合性实验，传统部分教学内容实现网络化等三方面对该课程的实验课部分进行了改革与实践，以期提高学生综合运用所学《土壤肥料学》的相关知识来解决生产实际问题的能力。     

时标轴上二阶Dirichlet边值问题的弱解（英文）

采用变分方法和临界点理论研究一个时标轴上二阶Dirichlet边值问题弱解的存在性.     

青藏铁路含保温夹层路基厚度与地温关系的研究

通过对青藏铁路风火山段含有保温夹层的路基建立均匀介质分层纯导热模型并运用分层近似解法求出冻土表层的温度函数,结合Lachenbruch给出的冻土层的理论温度表达式,得到了路基填料层、保温层、地表年平均温度与正弦变化温度的振幅比三者之间的隐式方程,并应用该方程对三者之间的关系进行了分析.     

兰州黄河岸边卵石层大吨位桩基自平衡法试验研究

对兰州深安黄河大桥进行桩基自平衡法试验。在对黄河岸边的岩土层进行桩基试验时,对桩基的极限侧阻力和端阻力标准值的取值提出建议,并在兰州地区进行自平衡法桩基试验时,对桩基侧摩阻力的取值提出建议。     

弱智儿童的脑机制及教育启示探析

弱智儿童的脑机制是我国特殊教育界尚未探讨的一个领域。从智力、弱智和学习的本质出发,探讨了弱智儿童脑发育的机制和脑活动机制,认为弱智儿童脑发育的正常机制因为先天、后天的遗传异常或损伤遭到了破坏,由此导致了神经系统的传导失能,并表现为神经环路的形成困难、传导的信息堵塞和消失这些主要的神经活动特点。提出了干预或教育弱智儿童的三大措施,包括食物或物质干预、文化给予以及感官训练与文化、言语的结合。     

Defining G protein-coupled receptor peptide ligand expressomes and signalomes in human and mouse islets

Introduction

Islets synthesise and secrete numerous peptides, some of which are known to be important regulators of islet function and glucose homeostasis. In this study, we quantified mRNAs encoding all peptide ligands of islet G protein-coupled receptors (GPCRs) in isolated human and mouse islets and carried out in vitro islet hormone secretion studies to provide functional confirmation for the species-specific role of peptide YY (PYY) in mouse islets.

Materials and methods

GPCR peptide ligand mRNAs in human and mouse islets were quantified by quantitative real-time PCR relative to the reference genes ACTB, GAPDH, PPIA, TBP and TFRC. The pathways connecting GPCR peptide ligands with their receptors were identified by manual searches in the PubMed, IUPHAR and Ingenuity databases. Distribution of PYY protein in mouse and human islets was determined by immunohistochemistry. Insulin, glucagon and somatostatin secretion from islets was measured by radioimmunoassay.

Results

We have quantified GPCR peptide ligand mRNA expression in human and mouse islets and created specific signalomes mapping the pathways by which islet peptide ligands regulate human and mouse GPCR signalling. We also identified species-specific islet expression of several GPCR ligands. In particular, PYY mRNA levels were ~ 40,000-fold higher in mouse than human islets, suggesting a more important role of locally secreted Pyy in mouse islets. This was confirmed by IHC and functional experiments measuring insulin, glucagon and somatostatin secretion.

Discussion

The detailed human and mouse islet GPCR peptide ligand atlases will allow accurate translation of mouse islet functional studies for the identification of GPCR/peptide signalling pathways relevant for human physiology, which may lead to novel treatment modalities of diabetes and metabolic disease.