犬腺病毒SY-45株不同大小蚀斑特性研究

应用蚀斑方法将SY－45毒株经过3次蚀斑纯化直到蚀斑大小相对稳定。从不同大小的蚀斑中挑选出三种蚀斑，大斑直径约3mm(简称LP）、中斑约2mm(简称MP）、小斑约1mm(简称SP）。分别在MDCK细胞上增殖并进行了三种不同大小斑毒对犬的毒力、免疫原性和在MDCK细胞上产毒量比较，以筛选最佳的疫苗株，试验结果表明用不同大小蚀斑病毒大剂量人工感染易感犬后，所有的试验犬临床症状和病理解剖学和病理组织学表现均正常；对挑选的4窝CAV HI抗体效价小于等于1：2的健康幼犬进行免疫试验，测定血清的中和抗体效价和血凝抑制抗体效价，结果表明：大斑毒的免疫原性要稍高于中斑毒，而明显高于小斑毒；不同大小蚀斑毒在MDKC细胞上产毒量差异很大，大斑毒可达10^7TCID50／mL、小斑毒达10^6TCID50／ml、小斑毒达10^4.5TCID^50/mL。综合所有试验结果表明：大斑毒株具有产毒量高、安全性好、免疫原性强的优点，是较为理想的疫苗株。     

链锯导板水平度检查与修整技术

链锯导板在使用中会经常出现各种变形，如扭曲、弯曲、凹凸不平等，针对各种变形，首先要认真进行检查，变形不同，检查的方法亦不相同，扭曲的检查，主要在金属平台上用手按动观察；弯曲变形要在金属平台上用较长的直尺检查；凹凸不平要在金属平台上用较短直尺检查。各种变形的修整均在金属平台上进行，不同的变形其修整方法不同，无论修整哪一种变形，锤击力都要一致，锤痕分布要均匀。     

重组逆转录病毒载体的包装

将3.7kb的LacZ基因片段克隆到含标志基因Neo的逆转录病毒载体，pLXSN与pLNCX的多克隆位点，构建了含有LacZ基因的重组逆转录病毒载体pLLSN和pLNCL.在测定了G418对饥装细胞系PA317的最小致剂量后（最小致死剂量为0.3g/L），通过脂质体Lipofectin与磷酸钙2种介质，分别将2种重组逆转录病毒载体导入包装细胞系PA317进行包装，并以0.3g/L，的G418进行筛选，得到多个G418抗性克隆，经扩大培养，传代，分别得到包装pLLSN与pLNCL的2株阳性细胞，电镜下可见阳性细胞的培养上清中具有逆转录病毒形态特征的成熟病毒粒子，本0研究为运用逆转录病毒载体系统，解决转角因效率低的问题奠定了基础。     

In vitro Plant Regeneration from the Mature Tissue of Navel Orange (Citrus sinensis L. Osbeck) by Direct Organogenesis

An efficient in vitro regeneration system by direct organogenesis from mature nodal and internodal stem segments of Newhall navel orange (Citrus sinensis L. Osbeck) was developed. Illuminating conditions together with plant growth regulators affected the adventitious bud regeneration frequency and efficiency. The initial 15 d darkness inoculation is beneficial for the adventitious bud regeneration. The highest regeneration frequency (85.2%) and bud formation efficiency (3.7 per responsive internodal stem segment) were obtained in the media supplemented with 1.0 mg L-1 BAP and 0.5 mg L-1 NAA. ABA at 0.2 mg L-1 positively affected the bud formation efficiency, which amounted to 8.5 buds per internodal segment in the presence of BAP at 1.0 mg L-1. The adventitious shoots successfully rooted and were transferred to the soil.     

鸡大肠杆菌病中草药佐剂多价灭活苗的研制——Ⅰ、疫苗生产工艺

采用鸡大肠杆菌多发病型菌株以及地方病型菌株作为制苗用菌种，保证了疫苗既具有一定的广谱性，又具有一定的特异性；采用液体通气培养方法，在一定程度上提高了菌数；采用中草药蜂胶作为佐剂不但可有效地提高机体的免疫功能，同时兼具有治疗，保健和促生长作用，另外蜂胶还可以增大抗原表面积，延长抗原在组织的贮存时间，可持久地释放抗原，保证了机体持续产生高效价抗体。     

以CP23重组蛋白为抗原建立检测微小隐孢子虫抗体间接ELISA方法的研究

摘要：以在E.coli高效表达的微小隐孢子虫子孢子表面抗原CP23为抗原，以辣根过氧化物酶(HRP)标记的山羊抗鼠IgG为二抗，建立了检测微小隐孢子虫抗体的间接ELISA方法。经检测筛选出最佳反应条件为1μg／孔纯化的E.coli表达的CP23抗原包被酶标板，用10％免血清进行封闭，以正常E.coli裂解上清液稀释待检血清。实验表明应用CP23重组蛋白作为诊断C.parvum抗原具有特异性高、抗原易纯化和成本低等特点。     

番鸭在南京地区的适应性观察

番鸭在南京地区进行冬、夏两批饲养,均有较强的适应性。试验结果表明:冬、夏两 批饲养的番鸭只平均重量差异不显著(P>0．05)。夏季与冬季的料重比分别为1:2．62和1: 3．07,冬季饲养的鸭子饲料利用率低,料重比大于夏季。冬季在塑料大棚中饲养番鸭精饲料减 少1／3,添加青粗饲料能达到同样的增重效果。温度与增重无相关关系,相对湿度与番鸭的增 重呈负相关(P<0．01)。鸭舍内平均温度在11．05℃-30．93℃之间,相对湿度在76．28％以 下,番鸭能正常生长发育。环境温度在9．8℃以下,番鸭的生长发育受阻,饲料利用率降低。相 对湿度在77％以上,其增重受到影响。特别在低温高湿的环境中,严重地影响番鸭的生长。在 相同的饲养期内,周平均温度9．8℃,平均相对湿度91％,番鸭周平均增重22 g,周平均温度 27．42℃,平均相对湿度71．29％,番鸭周平均增重355 g,相差333 g(P<0．01)。     

Role of angiotensin II and angiotensin II receptors in vascular smooth muscle cells migration

AIM:To determine the effects of Angiotensin II(AngII) on migration of rat smooth muscle cells and to investigate the mechanisms underlying Ang II action in the development of injured vascular disease. METHODS:VSMCs isolated from aortic media of Wistar rats and cultured by the modified explant method were adopted. In prersence and absence of AngII, the expression of AngII receptor and reorganization of the actin cytoskeleton of VSMCs were studied by immunocytochemistry technique, fluorocytochemistry technique. The migration assays were performed by a modified Boyden's chamber. And the effects of AT₁R antagonist (CV-11974), AT₂R antagonist (PD123319) on aforementioned target were studied.RESULTS:VSMCs migration was stimulated by addition of AngII. The dynamic reorganization of actin cytoskeleton may be an important mechanism by which AngII facilitates VSMC motility. The expression of AT₁R in VSMCs can be upregulated after treatment with AngII initially, then decreased gradually. The expression of AT₁R was downregulated by AT₁R antagonist. The effect of AngII on VSMCs migration was mediated by AT₁R, while AT₂R had no significant effect.CONCLUSION:The dynamic reorganization of actin cytoskeleton is required for AngII-induced VSMC migration, and this effect is mediated by AT₁R .     

Relation between TNF-α,TNFR I expression and apoptosis in oral lichen planus

AIM: To examine the expression and distribution of tumor necrosis factor-α (TNF-α), tumor necrosis factor receptor I (TNFR I) and apoptosis in oral lichen planus, and evaluate their roles and relation in the oral lichen. METHODS: Immunohistochemical technique and TUNEL were employed to study the expression of TNF-α, TNFR I and apoptosis in 50 cases of oral lichen planus and 10 normal oral mucosa specimens. RESULTS: Compared with the normal control group, TNF-α expression was upregulated in mononuclear cells in lamina propria and decreased in keratinocytes in oral lichen planus lesion (P<0.05). On the contrary, TNFR I expression was increased in keratinocytes and decreased in lamina propria in oral lichen planus lesion (P<0.05). The increased apoptosis index in keratinocytes and the decreased apoptosis index in lamina propria were found in oral lichen planus (P<0.05). CONCLUSION: The accelerated apoptosis of keratinocytes and the inhibition of lymphocytes apoptosis may contribute to the formation and progression of oral lichen planus.     

Chloride channels of platelets

Chloride channels distribute widely in the body, and participate in many physiological actions and regulatory processes. Based on their physiological roles and molecular structures, six kinds of chloride channels have been identified: (1) The chloride channels family; (2) Cystic fibrosis transmembrane conductance regulator; (3) Swelling-activated chloride channels; (4) Calcium-activated chloride channels; (5) The p64 (CLIC) gene family; (6) γ-aminobutyric acid and glycine receptors. The chloride channels do exist in platelets, and their appearances are dependent on the presence of intracellular calcium. Blocking agents of chloride channels inhibit the thrombin-activated platelet aggregation and the elevation of the intracellular calcium concentration in a dose-dependent manner. It is suggested that chloride channels play a role in the activation of platelets. In addition, chloride channels act on both the cell volume regulation and the intracellular pH regulation in platelets.