H2-calponin在细胞力学信号感知中的作用

H2-calponin是一种肌动蛋白细胞骨架结合蛋白,在平滑肌细胞和一些非肌肉细胞中均有表达,并且在发育及重建的组织中高表达。H2-calponin作为一种机械应力的胞内应答因子,受机械应力调节,通过与细胞骨架F-肌动蛋白(F-actin)及多种粘着斑蛋白相互作用,参与细胞力学信号感受与传导,在调节细胞增殖、分化、迁移以及胞质分裂等生理活动中起着重要作用。本文在介绍H2-calponin生化特征的基础上,对其在细胞应力感受及力学信号转导中的作用做一综述。     

运动训练对大鼠主动脉应力和NF-κB及c-fos表达的影响

目的：探讨不同强度运动训练对大鼠主动脉应力和NF-κB及c-fos表达的影响。方法：采用跑台训练方式,建立大鼠有氧运动和疲劳运动模型,运用免疫组织化学SABC法研究不同强度运动训练对大鼠主动脉VEC和VSMC中NF-κB及c-fos表达的影响。结果：胸主动脉血压的变化与对照组比较,有氧训练和疲劳训练均显著性升高（P〈0．05）,但有氧训练与疲劳训练之间差异不显著。与对照组比较,有氧训练大鼠VEC和VSMC中NF-κB和c-fos均显著性下调表达,胸主动脉张开角显著性升高（P〈0．05）,疲劳训练大鼠VEC和VSMC中NF-κB和c-fos均显著性上调表达（P〈0．05）。与有氧运动组比较,疲劳运动大鼠VEC和VSMC中NF-κB和c-fos表达与胸主动脉张开角升高均具有显著性差异（P〈0．05）。表明不同强度运动大鼠主动脉VEC中NF-κB和c-fos表达变化趋势不同,疲劳训练组表达的增加趋势更显著。结论：运动可引起大鼠主动脉VEC和VSMC NF-κB及c-fos表达的变化,且与运动强度关系密切。有氧训练引起的慢性剪切应力变化可使主动脉VEC和VSMC NF-κB加及c-fos显著性下调表达,与VEC和VSMC维持血管功能的稳态有关;疲劳训练可导致壁面摩擦剪切力、周向应力增加,过度的剪切力作用可引起主动脉VEC和VSMC NF-κB及c-fos显著性上调表达,血管张开角显著增加,血管发生非均匀生长,引起血管结构与功能的重塑。     

应用三维有限元分析髋臼骨结核软骨下骨塌陷的风险

目的建立人体髋臼骨结核三维有限元模型,探讨不同部位髋臼骨结核软骨下骨塌陷的风险。方法通过正常髋关节CT数据,利用Mimics软件和ANSYS有限元软件,建立正常髋关节三维有限元模型（模型A）、髋臼顶部骨结核（模型B）、髋臼中心部骨结核（模型C）、髋臼前部骨结核（模型D）、髋臼后部骨结核（模型E）三维有限元模型,模拟人体单脚站立进行加载,分析髋臼软骨下骨峰值Von Mises应力和初始微动值。结果建立了正常髋关节和不同部位髋臼骨结核三维有限元模型,各模型含节点269284,三维四面体单元184786个。通过加载分析结果显示：与正常髋关节相比,峰值Von Mises应力,依次增加84%、3%、21%、67%;髋臼软骨下骨初始微动值依次增加66%、11%、17%、29%。结论髋臼顶部结核软骨下骨峰值Von Mises应力和初始微动值最大,塌陷的风险最大。     

氧应力在产朊假丝酵母发酵生产谷胱甘肽过程中的作用

为了提高产朊假丝酵母合成GSH的能力,采用外界氧应力刺激的方式对细胞进行处理。稳定期之前添加H2O2对细胞生长有抑制作用,但稳定期添加H2O2对GSH的合成有促进作用,当H2O2添加总浓度为30 mmol.L-1时,无论采用一次性添加还是补加策略,都可以提高GSH的合成能力,胞内GSH质量分数提高幅度最大接近于20%,GSH产量最多提高17%。GSH分批发酵结果表明,稳定期补加H2O2对于产朊假丝酵母细胞来说,要比一次性添加H2O2对提高胞内GSH含量并最终增加GSH产量更为有效,该结果为实现氧应力刺激下GSH的过量合成提供了条件。     

Neuroprotection of Insulin against Oxidative Stress-induced Apoptosis in Cultured Retinal Neurons： Involvement of Phosphoinositide 3-kinase/Akt Signal Pathway

In order to investigate the neuroprotection of insulin in retinal neurons,we used retinal neuronalculture as a model system to study the protective effects of insulin against H_2O_2-induced cytotoxicity andapoptotic death.Primary retinal neuronal cultures were grown from retinas of 0-2-day old Sprague-Dawleyrats.Cell viability was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide assay.Apoptotic cell death was evaluated by the TdT-mediated digoxigenin-dUTP nick-end labeling assay,and byDNA laddering analysis.Phosphoinositide 3-kinase (PI3K) activity was measured using phosphoinositide4,5-bisphophate and [γ-~(32)P]ATP as substrate.Western blot analysis with anti-phospho-Akt (pS473) antibodywas performed to examine the level of phosphorylated Akt.We observed that treatment with 100μM H_2O_2for 24 h significantly decreased cell viability and induced apoptotic death of retinal neurons,and that pretreatmentwith 10 nM insulin significantly inhibited or attenuated H_2O_2-induced cytotoxicity and apoptosis.Pretreatmentwith LY294002,a specific PI3K inhibitor,abolished the cytoprotective effect of insulin.Insulin also stronglyactivated both PI3K and the downstream effector Akt.These results suggest that insulin protects retinalneurons from oxidative stress-induced apoptosis and that the PI3K/Akt signal pathway is involved in insulin-mediated retinal neuroprotection.     

Effect of Osmotic Stress in Early Stages of Ontogenesis on Root Respiration, Growth, Sugar Content, and Cell Injury in Maize Seedlings Differing in Drought Sensitivity

Cultivars of maize （Zea mays L.） with different sensitivity to drought were exposed to 0.3 mol/L sorbitol （-1.4 MPa water potential） for 24 h. Exposure to water deficiency significantly reduced the growth of both shoots （coleoptile and hypocotyl） and roots. Shoot growth was inhibited more than the growth of roots. Osmotic stress enhanced accumulation of soluble sugars. Electrolyte leakage, a cell injury index, was slightly increased after 0.3 mol/L sorbitoh Respiration was measured in the presence and absence of 2,6-dlchloro-phenol indophenoh 2,6-Dichloro-phenol indophenol did not influence respiration rates, because statistically equal results were observed under both conditions. Total respiration （VT） decreased after osmoticum treatment. There were no significant differences in the VT among the cultlvars analysed. The decrease In VT was caused by a decline In the activities and capacities of both cytochrome （Vcyt, Vcyt） and alternative pathway （Valt, Valt） of respiration. A high residual respiration （Vres） was observed, up to 27% of total uninhibited respiration. The result of uncoupler use clearly indicated that coupling was maintained after 24 h of osmotic stress. The recovery of the respiration rate was comparable with that of non-stressed control rates. According to these observations, no possible mltochondrial damage is expected. Water deficiency did not induce a stimulation of the alternative oxidase, so we assume that the stimulation of the alternative pathway is not related to drought stress resistance; rather, the function of the alternative pathway is to balance carbon metabolism and electron transport in a response to a changing environment.     

用脉冲电场凝胶电泳分析棉病囊霉及其突变体的染色体DNA

采用交变脉冲电场凝胶电泳和碱变性交变脉冲电场凝胶电泳方法,分析了棉病囊霉酵母菌及其2个不同的突变菌株的核型,得知此菌株含有5条染色体 DNA,而2株突变体的染色体 DNA 都没有大片段的缺失或双链断裂,但其稳定性不如野生型菌株的 DNA,而且存在单链断裂等碱不稳定性位点.     

完全固定桥修复前后基牙和牙槽骨表面的电测应力分析(二)

本文采用电阻应变片电测技术,在具有模拟双侧颞肌、嚼肌和颞下颌关节盘,牙列完整,(牙合)关系正常的头颅综合力学模型上,对完整牙列及局部缺牙区用完全固定桥修复后,不同(牙合)位上模拟产生正中(牙合)位下的早接触,测试分析基牙和牙槽骨受力后的应力分布。     

恐龙蛋壳的生物力学性质(Ⅰ)──在外力作用下恐龙蛋壳的应力分析

本文研究恐龙蛋在外压力作用下蛋壳内部的内力和应力变化规律,计算出蛋壳内部不同方位和不同方向上内力和应力的变化值。对四种不同类型恐龙蛋的蛋壳应力值进行了比较。得出了影响应力大小的因素和蛋壳在外压力作用下的破坏规律。     

Xyloglucan for Generating Tensile Stress to Bend Tree Stem

In response to environmental variation, angiosperm trees bend their stems by forming tension wood, which consists of a cellulose-rich G （gelatinous）-Iayer in the walls of fiber cells and generates abnormal tensile stress in the secondary xylem. We produced transgenic poplar plants overexpressing several endoglycanases to reduce each specific polysaccharide in the cell wall, as the secondary xylem consists of primary and secondary wall layers. When placed horizontally, the basal regions of stems of transgenic poplars overexpressing xyloglucanase alone could not bend upward due to low strain in the tension side of the xylem. In the wild-type plants, xyloglucan was found in the inner surface of G-layers during multiple layering. In situ xyloglucan endotransglucosylase （XET） activity showed that the incorporation of whole xyloglucan, potentially for wall tightening, began at the inner surface layers S1 and S2 and was retained throughout G-layer development, while the incorporation of xyloglucan heptasaccharide （XXXG） for wall loosening occurred in the primary wall of the expanding zone. We propose that the xyloglucan network is reinforced by XET to form a further connection between wall-bound and secreted xyloglucans in order to withstand the tensile stress created within the cellulose G-layer micro fibrils.