Determination of erythrocyte pyrimidine 5′-nucleotidase activity by31P nuclear magnetic resonance: Comparison of normal controls and multiple sclerosis patients

Summary A technique to assay erythrocyte pyrimidine 5-nucleotidase activity in situ using³¹P nuclear magnetic resonance spectroscopy is presented. The assay is chemically specific, simple and applicable to untreated lysates. A comparison of enzyme levels in normal controls and in multiple sclerosis patients employing the assay yielded no significant differences between both groups. Difficulties encountered in the quantitative analysis of the assay using¹H-NMR spectroscopy are briefly discussed.     

基于轻量化深度学习网络的数字仪表识别

数字式仪表常用于变电站、工厂等生产环境,是一种直观的设备监测仪器。然而当前数字式仪表的读取方式还依赖于人工巡检,手动记录等,这些传统的巡检方式来监测设备的运行状态大大降低了巡检效率。为了实现传统行业的数字化转型,本文提出基于轻量化深度学习的数字仪表识别方法,通过改进的YOLOv5的目标检测框架,针对数字仪表目标区域在整张图片大小不一致的情况,提出对于感兴趣区域（ROI）的迭代目标检测方法,首次检测将感兴趣区域进行检测并切割统一到相同的尺度,随后迭代检测网络针对感兴趣区域内的字符进行检测并分类,以达到精确读数的目的。为提升多尺度检测性能,本文采用Res2Net模块主干网络中的的残差模块。采用GIoU取代通用的IoU作为位置损失函数加速模型训练效果的收敛。实验表明,改进后的框架实现了99.62%的准确率和99.55%的召回率,相比基线网络分别提升了12.72%和5.85%。通过将框架在边缘计算平台上的终端部署,在实际生产中取代了人工巡检,实现了商业化运行。     

基于改进YOLOv5的遥感图像飞机目标检测

针对遥感图像中飞机检测尺寸大小不一、背景复杂导致的难以识别问题,提出一种基于YOLOv5网络模型的改进方法。首先,在YOLOv5网络模型中融入Swin-Transformer模块,使网络全局建模并使全维度信息交互,以提升网络的特征提取能力;其次,对损失函数进行优化,引入SIOU损失函数以考虑真实框和预测框之间的向量角度问题。对比实验表明,优化前后网络模型检测精度均为95.3%。在检测精度相同的情况下,改进后的网络模型召回率为91.2%,比改进前提升0.6个百分点;改进后平均检测精度mAP_0.5为95.7%,比改进前提升0.2个百分点。结果表明,改进后的YOLOv5网络模型能在一定程度上提升遥感图像中飞机目标检测性能。     

Metabolism of 3β-hydroxycholest-5-en-26-oic acid in hamsters

Summary Metabolism of 26-hydroxycholesterol to 3-hydroxychol-5-en-24-oic acid and other C24-bile acids has been expected to occur by way of 3-hydroxycholest-5-en-26-oic acid in studies in vitro. 3-Hydroxycholest-5-en-26-oic acid was infused intravenously into bile fistula hamsters and the following C24-bile acids were identified: 3-hydroxychol-5-en-24-oic acid, lithocholic acid, chenodeoxycholic acid, and a small amount of cholic acid.     

Bovine microvascular endothelial cells of separate morphology differ in growth and response to the action of interferon-γ

Five cell types recently isolated from the bovine corpus luteum differed in their epithelioid morphology and their cytoskeleton, but shared common criteria of microvascular endothelial cells^1,2. To give strong evidence for the separate entity, the growth rate of the 5 phenotypically different cells was studied. They were seeded at low density on day 0. Most of these cells were treated with 200 to 1000 U recombinant bovine interferon- (IFN-) for 3 days. The untreated remainder served as controls. Cell counts were made for all cultures on days 4, 7, 10 and 13. morphology: 13 d after treatment with IFN- senescent cells as well as intact cells occurred in cultures of cell types 1 to 4. Cultures of cell type 5 were apparently unchanged and resembled their untreated counterparts. Desminpositive cells in cultures of cell type 2 developed cell processes. Growth rate: In the absence of IFN-, the growth rate was high for cell types 3 and 4, moderate for cell type 1, and low for cell types 2 and 5. The presence of IFN- caused anti-proliferative effects. These were higher for cell types 3 and 4 than for cell types 1 and 2. IFN- could be cytotoxic on cell type 3. In contrast, the cytokine tended to support the cell growth of cell type 5. These findings substantiate the postulate that endothelial cells exhibiting separate morphology in culture also function differently.     

含双二苯基膦戊烷铜(Ⅰ)配合物的合成与性质

室温,氮气氛下,铜（Ⅱ）盐和双二苯基膦戊烷（ｄｐｐｐ５）在溶液中通过还原取代反应合成了８种铜（Ⅰ）配合物（１．［Ｃｕ（ｄｐｐｐ５）］２（ＢＦ４）２,２．［Ｃｕ２（ｄｐｐｐ５）２（Ｃ８Ｈ３Ｏ２ＳＦ３）２］,３．［Ｃｕ２（ｄｐｐｐ５）３］（ＣＣｌ３ＣＯＯ）２,４．［ＣｕＢｒ（ｄｐｐｐ５）］２,５．［Ｃｕ２（ｄｐｐｐ５）Ｃｌ２］,６．［Ｃｕ２（ｄｐｐｐ５）３］（ＣＨ３ＣＯＯ）２,７．［Ｃｕ（ｄｐｐｐ５）（ＮＯ３）］,８．［Ｃｕ２（ｄｐｐｐ５）３］（ＣｌＯ４）２）。通过元素分析、红外光谱、热重、摩尔电导测定对其进行表征,表明这是一种行之有效的有机膦配合物的合成方法。     

人非小细胞肺癌rasP^21和CD44的表达及意义

用免疫组化ＬＳＡＢ法检测４６例非小细胞肺癌ｒａｓＰ２１和ＣＤ４４的表达。结果：ｒａｓＰ２１的阳性率鳞癌为５９％,腺癌６３％;ＣＤ４４的阳性率鳞癌为４１％,腺癌６３％。统计学分析证明：不同临床分期的ｒａｓＰ２１表达强度有显著性差异（Ｐ＜００１）;有淋巴结转移与无淋巴结转移的ＣＤ４４表达程度有显著性差异（鳞癌Ｐ＜００１,腺癌Ｐ＜００２５）;ｒａｓＰ２１与ＣＤ４４表达强度两者无相关性（Ｐ＜００５）。结论：ｒａｓＰ２１的表达与预后不良有关,ＣＤ４４的表达与淋巴结转移有关。     

Cloning, construction of prokaryotic expression vector and expression ofEscherichia coli cytosine deaminase gene

Cytosine deaminase gene ofEscherichia coli strain H-30 was cloned, and its initiation codon of ‘GTG’ was mutated to ‘ATG’ by PCR. Prokaryotic recombinant expression vector pBV220-CD was constructed. Clone with high enzyme activity were selected by detecting their specific activity of cytosine deaminase. 5-FC(5-FC, 5-fluorocytosine) could induce the lethal toxicity to cells containing active CD gene. DNA sequence analysis indicated that there were 16 altered bases and 5 of them resulted in the alteration of amino acids in predicted peptide by comparing DNA sequence of the clone H-30-CD-11 with high enzyme activity with CD gene reported in Gene Bank.     

Two tyrosines in CD3ε-ITAM are required to induce T lymphocyte apoptosis

CD3ε of T cell antigen receptor complex (TCR/CD3) plays an important role in the resembling of the complex and activation signaling through its conservative immunoreceptor tyrosine-based activation motif (ITAM) in the cytoplasmic tail. Previous study showed that a chimera molecule, consisting of the extracellular-transmembrane domain of human CD8α fused to the cytoplasmic domain of CD3ε, induced apoptosis of T lymphocytes, indicating that apoptotic signals were transduced through the CD3ε- ITAM. To elineate involvement of the two tyrosines in apoptotic signaling pathway, cDNAs with mutations at Y170F, Y181F and Y170F/Y181F in CD8-ε-ITAM were made by point mutation and PCR, and then cloned into pcDNA3 eukaryotic expression vectors. Stable expression cell lines were established after transfection of the expression vectors into CD8+- Jurkat T lymphocytes. Stimulation of these cell lines with anti-CD8 monoclonal antibody showed that only the cells with expression of wild type chimera CD8-ε died by apoptosis, but not those cells with expressions of mutated CD8-ε chimera, indicating that the two tyrosines in CD3ε-ITAM were required for the apoptotic signal transduction in T lymphocytes.     

大洋多金属结核中五氧化二磷分析方法

试样经ＮａＯＨ溶融,水浸取后,使Ｆｅ、Ｍｎ、Ｃｕ、Ｃｏ、Ｎｉ等共存元素形成氢氧化物沉淀与磷分离,滤液中的磷用磷钼黄光度法测定。方法简便、快速、精密度好、准确度高。经对标准物质ＧＢＷ０７２４９测定,结果与推荐值吻合,ＲＳＤ（ｎ＝１０）〈１．４％。