应用赤霉菌粗毒素测定小麦品种的抗赤霉病性

小麦赤霉菌 Gibberella zeae(Schw.)Petch 在麦粒培养基上进行固体产毒培养,从中提取粗毒素。用粗毒素溶液处理小麦抗感赤霉病不同品种萌动—致的种子以及—叶期幼根和叶鞘。用 DDS-11A 型电导仪测定细胞渗透性变化。结果表明,在粗毒素作用下,小麦根、芽生长受抑制。但抗病品种受抑轻,感病品种受抑重。抗感品种幼根和叶鞘细胞渗透性的变化差异明显。用赤霉菌粗毒素测定细胞渗透性的变化,有可能作为鉴定小麦品种抗赤霉病的一个生理指标。     

中草药对建鲤非特异性免疫功能的影响

用添加中草药的鲤配合饲料饲喂建鲤(Cyprinnus var．Jian)后,测定了建鲤非特异性免疫指标。饲喂药饵Ⅰ 10、15、30 d后,氯化硝基四氮唑兰(NBT)阳性细胞数分别为 27±3．45、39±6．04和 38±4．81,溶菌酶活力分别为 0．013±0．0017、0．018±0．0053和 0．021±0．0037;饲喂药饵 Ⅱ 10、15、30 d后,NBT阳性细胞数分别为 30±2．23、87±8．57和82±7．42,溶菌酶活力分别为0．015±0．0020、0．044±0．0017和0．033±0．0011;而对照组NBT阳性细胞数分别为28±2．18、27±4．05和29±3．56,溶菌酶活力分别为0．013±0．0010、0．012±0．0031和0．015±0．0046。结果表明,饲喂药饵Ⅱ 15、30d后的NBT阳性细胞数和溶菌酶活力均显著高于对照组(P＜0．05)。因而,本配方的中草药按质量分数为1．0%的量加入到饲料中,既能明显提高建鲤的吞噬细胞、中性粒细胞和巨噬细胞的数量,又能提高其溶菌酶的活力,从而明显提高建鲤的非特异性免疫能力。     

传染性法氏囊病疫苗免疫种鸡后子代雏鸡的免疫学变化

应用现代免疫学新技术对传染性法氏囊病 (IBD)疫苗免疫种鸡后 ,其子代雏鸡外周血液和免疫器官组织的免疫学变化进行了动态研究。结果发现 :传染性法氏囊病疫苗免疫种鸡后 ,其子代雏鸡外周血液 T、B细胞数量和 Ig G,Ig M,Ig A含量及免疫器官组织的 T细胞、Ig G,Ig M,Ig A抗体生成细胞数量均不同程度地高于未免疫的相应对照雏鸡 ,表明 IBD疫苗免疫母鸡后 ,子代雏鸡外周血液和免疫器官组织的体液免疫和细胞免疫功能明显增强。而传染性法氏囊病超强毒攻击子代雏鸡后 ,未免疫的子代雏鸡 ,外周血液和免疫器官组织的上述各项指标均明显低于疫苗免疫的子代雏鸡 ,这与 IBDV感染雏鸡后 ,其免疫器官组织严重损害 ,淋巴细胞变性坏死等有关 ,也是导致感染雏鸡免疫抑制的基础     

水稻花培获得大群体健壮绿苗的研究

通过使用混合激素诱发籼稻871015、871109花粉愈伤形成胚性细胞;对籼稻花粉胚性细胞团和粳稻绿芽丛进行分割培养,快速繁育大群体绿苗获得成功。籼稻两个组合的8块胚性细胞团,在两个月内经3—5次切割培养获得绿苗12690株;粳稻花培绿芽丛仅经一次分割培养后的净增绿苗率127.2%,大幅度地提高了水稻花药培养再生绿苗率。分割培养的再生苗,健壮的形成特征:苗粗、浓绿、根多、洁白。良好的生理素质:发根力强,平均每棵试管苗多增根1.8条,根长度增长168.4%;平均每棵再生苗鲜重和干重分别增加0.29克和0.175毫克。     

流式细胞术检测TcR Vα24/Vβ11双阳性NKT细胞及其在HCV感染者中的应用

目的研究丙肝病毒感染者外周血NKT细胞含量与HCV感染状态之间的相关性.方法应用流式细胞术检测TcR Vα24/Vβ11双阳性NKT细胞.结果抗-HCV阳性且HCVRNA也阳性的病例NKT细胞数量明显低于抗-HCV阳性而HCV RNA阴性的病例（P〈0.01）,明显低于正常对照组（P〈0.05）.结论由于NKT细胞数量减少或活化受阻,造成HCV的持续感染,不利于病毒的清除;另一方面,由于肝内有HCV的存在,NKT细胞大量向肝内趋化,导致外周血的数量相对减少.     

余甘子精粉的体外抗氧化活性分析

The antioxidant activities in vitro of refined powder of Phyllanthus emblica L. were detected by methods based on chemical measurement and cell modeling. The results of anti-peroxidation ability and iron reduction ability trials showed that the refined powder of P. emblica L. had strong ability of anti-peroxidation, and it increased with the increasing of concentration with a clear dose-response relationship. When the concentration reached 800 μg·mL^-1, the ability of anti-peroxidation was almost equal to the positive control VC with the same concentration. Meanwhile, it also had iron reduction ability that accompanied by significant dose-response relationship. By in vitro cell culture method, H₂O₂ was used to induce SH-SY5Y cells damages to establish the cell model of oxidative damage. The author detected the effect of different concentrations of powder on cell survival rate for the model cells by MTT assay. The results indicated that refined powder could show better protective effect to oxidative damaged SH-SY5Y cells in the range of 600 1 200 μg·mL^-1. When the concentration reached 1 200 μg·mL^-1, the cell survival rate was the highest and refined powder exhibited the best antioxidant activity. Both methods proved the strong antioxidant activities of refined powder of P. emblica L. in vitro.     

高效氯氰菊酯对小鼠卵巢生殖功能的影响及维生素E的干预作用

为探究高效氯氰菊酯 (beta-cypermethrin, β-CP) 对雌性小鼠卵巢生殖功能的影响及维生素E (vitamin E, VE) 的干预作用,将雌性昆白小鼠随机分为6 组:空白对照组 (花生油处理)、β-CP不同剂量 (10、20、40 mg/kg) 处理组、VE保护组 (20 mg/kg β-CP+20 mg/kg VE) 和VE组 (20 mg/kg VE),连续灌胃10 d。灌胃结束后取小鼠卵巢组织,观察组织结构的病理变化,采用免疫组化法、蛋白免疫印迹试验及RT-PCR方法检测卵巢中StAR蛋白含量及casp-3、casp-8、INHα和INHβB 基因mRNA表达的变化。结果显示:与对照相比,10、20和40 mg/kg的β-CP处理均使小鼠卵巢组织结构发生了损伤,使组织中StAR蛋白的浓度分别降低了18.8%、36.3%和40.3%,casp-3基因的表达分别升高了16.0%、26.7%和52.9%,INHα基因的表达分别升高了34.5%、83.6%和228.7%,INHβB基因的表达分别升高了7.5%、39.2%和52.7%;20和40 mg/kg的β-CP处理使得casp-8基因的表达分别升高了27.1%和36.7%。上述处理组与对照组的差异均达显著水平 (P＜0.05)。与 20 mg/kg β-CP处理组相比,VE 保护组的StAR蛋白含量也显著增多 (P＜0.05)。研究表明,β-CP对小鼠卵巢具有毒性作用,这与β-CP抑制StAR蛋白的合成,上调casp-3、casp-8、INHα及INHβB基因的表达有关;添加VE对小鼠卵巢有一定的保护作用,这与VE可减弱β-CP对StAR蛋白合成的抑制作用有关。     

miR-140-3p inhibits viability,invasion and migration of non-small-cell lung cancer A549 cells by targeting PD-L1

AIM: To explore the target relationship between microRNA-140-3p (miR-140-3p) and programmed cell death ligand 1 (PD-L1) and their effect on the viability, migration and invasion of non-small-cell lung cancer A549 cells.METHODS: RT-qPCR was used to detect the miR-140-3p expression in HLF-1, A549 and H1299 cells, and then the A549 cells with the most significant difference were selected as the subsequent research object. TargetScan software and dual-luciferase reporter assay were performed to predict and confirm the target relationship between miR-140-3p and PD-L1. RT-qPCR and Western blot were used to determine the effects of miR-140-3p mimic and inhibitor on PD-L1 expression level. MTT assay was used to detect the viability of A549 cells. Transwell assay was performed to detect the migration and invasion abilities of the A549 cells.RESULTS: miR-140-3p was significantly down-regulated in the A549 cells and H1299 cells (P<0.05). Transfection with miR-140-3p mimic decreased the expression of PD-L1 and inhibited the viability, migration and invasion of the A549 cells. Transfection with pcDNA3.0-PD-L1 reversed the inhibitory effect of miR-140-3p on the viability, migration and invasion of the A549 cells.CONCLUSION: miR-140-3p inhibits the viability, migration and invasion of A549 cells by targeting PD-L1.     

Effect of CHOP expression knock-down on apoptosis of renal tubular epithelial cells

AIM:To study the effect of C/EBP homologous protein (CHOP) on the apoptosis of renal tubular epithelial HK2 cells. METHODS:The serum mRNA levels of CHOP in the patients with acute kidney injury and healthy controls were detected by qPCR. In vitro, renal tubular epithelial HK2 cells were divided into control group, negative group (transfected with negative control siRNA), si-CHOP group (transfected with CHOP siRNA), and induced by transforming growth factor-β1 (TGF-β1). The viability of the cells was measured by MTT assay, and the apoptotic rate was analyzed by flow cytometry. The protein levels of nuclear antigen Ki-67, proliferating cell nuclear antigen (PCNA), caspase-3 and cleaved caspase-3 were determined by Western blot. RESULTS:Compared with the healthy controls, the serum mRNA levels of CHOP in the patients with acute kidney injury were increased significantly (P<0.05). Transfection with CHOP siRNA significantly decreased the expression of CHOP in the renal tubular epithelial HK2 cells (P<0.05). Knock-down of CHOP expression by siRNA significantly increased the viability of renal tubular epithelial HK2 cells (P<0.05), decreased the apoptotic rate (P<0.05), increased the expression of Ki-67 and PCNA (P<0.05), and down-regulated the protein level of cleaved caspase-3 (P<0.05). CONCLUSION:The serum mRNA levels of CHOP were increased in the patients with acute kidney injury. Knock-down of CHOP expression inhibits the apoptosis of renal tubular epithelial cells by regulating the expression of proliferation-and apoptosis-related proteins.     

内生菌与雷公藤细胞悬浮共培养的生理生化特性

将2株雷公藤内生真菌Fusarium oxysporum NS33与Penicillium steckii NS6、2株内生细菌Enterobacter cloacae sub sp LG3与Serratia marcescens LY1及其组合分别与雷公藤细胞悬浮共培养,对不同培养体系内雷公藤细胞的生长及其生理生化特征进行研究。结果显示,在共培养前期,与对照相比,接种单一内生菌株提高了细胞的干重,其中菌株NS6的促生效果最明显;而在共培养后期,无论是单一内生菌还是混合内生菌均对细胞生长具有抑制作用。内生真菌和菌株组合处理的培养液p H值有明显的升高,而内生细菌LY1则明显降低了培养液的p H值,其具有产酸性。另外,当雷公藤细胞同混合菌株共培养时,培养基中总糖消耗量是最大的,而接种单独菌株时则对细胞可溶性蛋白含量具有一定的提高作用。接种内生菌会影响雷公藤细胞的POD、CAT及SOD活性,与对照相比,接种单独菌株会更加提升POD与CAT的活性,而细胞MDA含量则明显下降。