干旱与氧化胁迫对小麦根氧化还原状态和叶片ABA积累的影响

通过分析一氧化氮(nitric oxide,NO)、活性氧(reactive oxygen species,ROS)和干旱胁迫对小麦根氧化还原状态和叶片脱落酸(abscisic acid,ABA)积累的影响,探讨了干旱胁迫下NO和H2O2调节ABA合成的可能机制。结果表明:干旱胁迫处理初期小麦根还原型谷胱甘肽含量降低、抗氧化酶活性发生振荡变化,细胞氧化还原状态向氧化型转变。NO和H2O2能模拟干旱胁迫的作用使细胞状态向氧化型转变,还可以使小麦叶片ABA积累量上升。干旱胁迫下NO和H2O2对ABA合成的调节作用可能是通过调节细胞氧化还原状态进行。     

白喉毒素类免疫毒素研究进展

白喉毒素类免疫毒素是将缺失天然受体结合活性的白喉毒素片段或突变体与抗体或细胞因子偶联而得到的一类新型导向药物,它可特异性识别并结合靶细胞,通过发挥其ADP核糖基化活性而抑制细胞蛋白合成,引发细胞凋亡。由于白喉毒素类免疫毒素能高效、特异地杀伤特定靶细胞,而使其在肿瘤等疾病的药物开发中暂露头角。综述了基于白喉毒素的免疫毒素的研制现状与应用前景 。     

圆柏属常绿木本植物叶片水分、渗透调节物质的季节变化与抗冷冻性的关系

以祁连圆柏（Sabina przewalskii）和圆柏（Sabina chinensis）为材料,研究了圆柏属植物的抗冷冻性与叶片水分和渗透调节物质季节变化的关系。结果表明,随秋季气温下降,叶片组织相对含水量（RWC）和自由水含量（FWC）下降,束缚水含量（BWC）、脯氨酸（Pro）、游离氨基酸（FAA）、可溶性蛋白质（SP）和可溶性糖（SS）含量增加,翌年春季气温回升,相对含水量和自由水含量增加,束缚水含量下降,有机渗透调节物再次增加。有机渗透调节物在秋末冬初及初春的增加正好与圆柏属植物抗冻锻炼及脱冻恢复生长的时间相吻合,因而是植物抗冻及脱冻适应的重要生理响应,在降低细胞冰点、防止细胞结冰引起的膜机械伤害、抑制膜脂过氧化、保护膜稳定性方面具有重要作用。祁连圆柏的相对含水量和自由水含量均低于圆柏,3种有机渗透调节物含量均高于圆柏,表明祁连圆柏在抗冷冻性诱导中具有更广泛的适应性策略。     

联合国教科文组织生命科学伦理学项目实施与法医专业本科生素质教育与专业外语教学创新实践的教学研究

如何最大程度地发挥学校的教学潜能和优势,选择最为有效的教学方法来提高法医专业本科学生的素质能力和专业外语水平,已经成为新形势下高校教学改革的重要内容.本文结合笔者工作实际,讨论开展联合国教科文组织生命科学伦理学项目实施与法医专业本科学生素质教育与专业外语教学创新实践教学研究的相关问题.     

Restoring the youth of aged red blood cells and extending their lifespan in circulation by remodelling membrane sialic acid

Membrane sialic acid (SA) plays an important role in the survival of red blood cells (RBCs), the age‐related reduction in SA content negatively impacts both the structure and function of these cells. We have therefore suggested that remodelling the SA in the membrane of aged cells would help recover cellular functions characteristic of young RBCs. We developed an effective method for the re‐sialylation of aged RBCs by which the cells were incubated with SA in the presence of cytidine triphosphate (CTP) and α‐2,3‐sialytransferase. We found that RBCs could be re‐sialylated if they had available SA‐binding groups and after the re‐sialylation, aged RBCs could restore their membrane SA to the level in young RBCs. Once the membrane SA was restored, the aged RBCs showed recovery of their biophysical and biochemical properties to similar levels as in young RBCs. Their life span in circulation was also extended to twofold. Our findings indicate that remodelling membrane SA not only helps restore the youth of aged RBCs, but also helps recover injured RBCs.     

日本沼虾与海南沼虾的人工种间杂交及其同工酶分析

日本沼虾(Macrobrachium nipponense),又名青虾,是我国重要的淡水养殖虾类。但近年来,青虾的性状出现了严重的退化,包括性早熟、规格变小、商品率低、抗病力下降等,严重地影响了青虾养殖业的效益,因此有必要对青虾进行遗传改良。由于虾类种内变异很小1,种间杂交可能是遗传改良的有效途径,但沼虾类的人工种间杂交未见有成功的报道。本文主要研究日本沼虾与海南沼虾(Macrobrachium hainanense)的人工种间杂交,并借此探索虾类的遗传改良途径。       

The P2Y2 Nucleotide Receptor Mediates the Proliferation and Migration of Human Hepatocellular Carcinoma Cells Induced by ATP

ATP is an abundant biochemical component of the tumor microenvironment and a physiologic ligand for the P2Y₂ nucleotide receptor (P2Y₂R). In this study, we investigated the effect of ATP on the cellular behavior of human hepatocellular carcinoma (HCC) cells and the role of P2Y₂R in ATP action and aimed to find a new therapeutic target against HCC. The experiments were performed in native isolated human HCC cells, normal hepatocytes, human HCC cell lines, and nude mice. We found that the mRNA and protein expression levels of P2Y₂R in native human HCC cells and the human HCC cell lines HepG2 and BEL-7404 were enhanced markedly compared with human normal hepatocytes and the normal hepatocyte line LO2, respectively. ATP induced intracellular Ca²⁺ increases in HCC cells and promoted the proliferation and migration of HCC cells and the growth of HCC in nude mice. The P2Y receptor antagonist suramin, P2Y₂R-specific shRNA, the store-operated calcium channel inhibitors 2-aminoethoxydiphenyl borate (2-APB) and 1-(β-3-(4-methoxy-phenyl) propoxyl-4-methoxyphenethyl)1H-imidazole-hydrochloride ({"type":"entrez-protein","attrs":{"text":"SKF96365","term_id":"1156357400","term_text":"SKF96365"}}SKF96365), and stromal interaction molecule (STIM1)-specific shRNA inhibited the action of ATP on HCC cells. In conclusion, P2Y₂R mediated the action of ATP on the cellular behavior of HCC cells through store-operated calcium channel-mediated Ca²⁺ signaling, and targeting P2Y₂R may be a promising therapeutic strategy against human HCC.