Role of ghrelin in cell protection by up-regulating HSP70 through ERK1/2 signaling pathway in PC12 cells

AIM:To study the role of ghrelin in cell protection by up-regulating heat shock protein 70 (HSP70) and inhibiting apoptosis induced by oxidative stress through extracellular regulated protein kinases 1/2 (ERK1/2) signaling pathway in the PC12 cells. METHODS:Sodium nitoprusside (SNP) was used to induce oxidative stress injury in the PC12 cells. The cultured PC12 cells were divided into SNP-injured group (incubated with SNP at 0.5 mmol/L for 6, 12, 18 and 24 h), ghrelin pretreatment group (ghrelin at 100 nmol/L was given 30 min before adding SNP); HSP70 inhibitor group (quercetin at 10 μmol/L was added 60 min before ghrelin treatment), ERK inhibitor group (ERK 1/2 inhibitor PD98059 was added 60 min before ghrelin treatment) and control group (added same amount of culture medium only). The apoptotic rate was detected by flow cytometry. The protein expression was determined by Western blot and immunocytochemistry. RESULTS:Compared with control group, the apoptotic rate of PC12 cells in SNP-injured group was significantly increased (P<0.05). Compared with SNP-injured group, ghrelin (100 nmol/L) pretreatment significantly inhibited SNP-induced apoptosis of PC12 cells (P<0.05), and significantly up-regulated the protein expression of HSP70 (P<0.05). Time-effect analysis showed that ghrelin had the most significant effect at 18 h after SNP injury. Quercetin, an inhibitor of HSP 70, significantly reduced the anti-apoptotic effect of ghrelin (P<0.05). Ghrelin pretreatment promoted the phosphorylation of ERK1/2. ERK1/2 inhibitor PD98059 significantly inhibited the effects of ghrelin on up-regulation of HSP70 expression (P<0.05). CONCLUSION:Ghrelin upregulates the expression of HSP70 and inhibits the apoptosis in the PC12 cells induced by oxidative stress by promoting the phosphorylation of ERK1/2.     

油菜素内酯浸根对水稻水卷苗机插植伤的修复效应

目的 探究油菜素内酯(Brassinolide, BR)浸根对机插水卷苗栽后本田生长及产量的影响。方法 以宁粳8号为试验材料,分析不同浓度BR(T1、T10、T20,分别表示水培营养液中BR浓度为1 mg/L、10 mg/L、20 mg/L)浸根对水卷苗机插本田后返青活棵及产量的影响,以正常水培营养液处理为对照(CK)。结果 BR浸根(T1、T10、T20)能够促进水稻地上部生长,栽插本田21d后株高较CK分别增加11.68%、8.12%和7.61%;BR浸根对水卷苗栽后根系的促生作用更为明显,不同浓度BR浸根对水卷苗栽后根长、根表面积、根尖数、根体积、根直径、根质量和根冠比均产生了显著影响,其中根尖数以低浓度BR处理效果更优,而其他根系指标均以高浓度BR处理效果更优。与CK相比,不同浓度BR浸根降低了叶片过氧化氢浓度(至移栽后12 d,分别降低12.50%、23.25%和22.25%),增强了叶片抗氧化酶活性;与移栽当天相比,移栽后第2天BR浸根处理叶片中玉米素(ZT)浓度迅速增加(分别为197.27%、153.11%和243.78%),而CK增加缓慢(2.94%),根系表现一致,且根系中生长素(IAA)浓度显著高于CK;同时BR处理在栽后一周内赤霉素(GA₃)浓度均明显高于对照。与CK相比,T10处理显著提高了每穗粒数和结实率(分别为15.04%和6.62%),T20处理显著提高了结实率(6.17%),但BR处理千粒重均显著下降,最终产量T10和T20处理较CK分别提高5.11%和7.99%。结论 适当浓度的BR(T10~T20)浸根能减轻水卷苗机插植伤,提高抗氧化酶活性,降低H₂O₂含量,提高ZT、GA₃和IAA浓度,高效地促进根系生长,提高了每穗粒数和结实率。本研究可为减轻机插植伤,促进机插水稻高产稳产提供理论依据和技术参考。     

玉米热激蛋白ZmHSP70-12基因的克隆及表达分析

热激蛋白70(HSP70)是原核和真核细胞中普遍存在的一种高度保守的分子伴侣。从玉米中克隆1个HSP70家族成员。该基因cDNA序列全长为1 992 bp,开放阅读框为2 352 bp,编码663个氨基酸,蛋白质分子量约75.0 kD。蛋白结构预测及同源比对分析表明,该基因编码蛋白含ATPase位点和HSP70保守结构域,与拟南芥AtHSP70-12序列高度相似,命名为ZmHSP70-12。蛋白亚细胞定位显示,ZmHSP70-12蛋白在内质网中表达。实时荧光定量PCR分析表明,ZmHSP70-12对非生物胁迫高温、干旱均具有明显的应答反应,推测ZmHSP70-12是玉米中与胁迫逆境相关的基因。     

定量泵负载敏感系统卸荷压力冲击抑制研究

定量泵负载敏感系统在快速卸荷时容易出现压力冲击现象,对系统的可靠性和寿命产生较大危害。三通压力补偿阀是定量泵负载敏感系统中关键的调压元件,本文以三通压力补偿阀为切入点,建立定量泵负载敏感系统功率键合图模型,基于键合图模型推导系统的状态方程,建立Matlab动态仿真模型,探讨系统卸荷压力冲击的抑制方案。基于系统仿真模型,首先对系统卸荷压力冲击的仿真与试验进行对比,验证了仿真模型的正确性;然后,针对三通压力补偿阀的系统压力腔阻尼、阀芯直径、Ls腔阻尼、阀口锥角等关键参数,对卸荷压力冲击影响规律进行仿真;最后,基于关键参数对卸荷压力冲击影响规律的分析,提出了一种"小阀芯、双阀口"型三通压力补偿阀结构优化方案,并对其卸压冲击抑制效果进行了仿真和试验。结果表明,该方案可以有效抑制卸荷压力冲击,优化后系统卸压冲击压差比原系统降低了89%,卸荷压力降低了20%,进一步实现了节能。     

一个水稻小热休克蛋白的异源表达及寡聚特性分析

【目的】在前期研究中,本实验室已克隆了一个水稻小热休克蛋白基因(OsSHSP17.6),并发现该基因的表达明显受到热激和病毒侵染调控,表明该蛋白可能在逆境胁迫过程中起重要作用。本研究的目的在于进一步明确OsSHSP17.6的特性。【方法】在本研究中,进一步将该基因亚克隆至原核表达载体p ET-32a并导入大肠杆菌E.coli BL21(DE3)pLysS诱导表达,通过亲和层析的方法纯化了该重组蛋白,进一步用于非变性聚丙烯酰胺凝胶电泳和Western blotting分析。【结果】异源表达的重组OsSHSP17.6能减轻IPTG对宿主菌的毒害。非变性聚丙烯酰胺凝胶电泳和Western blotting分析显示纯化的重组OsSHSP17.6蛋白在体外能形成同源二聚体和寡聚体。【结论】这些结果支持OsSHSP17.6是一个有功能的分子伴侣蛋白并表明该蛋白可能通过形成同源寡聚体的方式参与逆境胁迫反应,这为进一步明确OsSHSP17.6的功能机制奠定基础。     

土壤中联苯菊酯样品不同制备方法比较研究

[目的]研究土壤中联苯菊酯样品索氏提取法与震荡提取法之间的差异。[方法]在白蚁预防施工过程中,随机抽取8个样品。分别用索氏提取法和震荡提取法进行样品的提取,再用气相色谱检测。[结果]试验提供8个样品进行对比试验,其中6个样品经索氏提取后检测浓度明显高于震荡提取后检测浓度,只有2个样品前者浓度低于后者。[结论]索氏提取法可以用于土壤中联苯菊酯样品的提取。     

Induction of meiotic gynogenesis in bagrid catfish (Pseudobagrus ussuriensis) with homologous sperm and its confirmation for female homogamety

The bagrid catfish, Pseudobagrus ussuriensis, exhibits significant sexual dimorphism in growth rate and body size with males growing faster than females. Therefore, an all‐male culture can dramatically increase the output and profitability of fishery products. According to the monosex breeding route, super‐male individuals’ acquirement by XY male sex reversal and artificial gynogenesis is the key step. An effective protocol to induce meiotic gynogenesis using homologous sperms has been developed in this study. The most effective UV irradiation for sperm genetic inactivation was found to be at a distance of 20 cm with 66 μW/cm² light intensity for 25 min. Optimal treatment for cold shock was 5 min post‐fertilization at 0‐4°C for 30 min, which gave the best survival rate of 13.65 ± 2.87%. The sex ratio in the meiotic gynogens showed a significant female‐biased deviation (p < .05); thirty meiogynogens and their parents were further analysed using a male‐specific AFLP marker, of which only the male parent produced a male‐specific DNA band of 412 bp. These results indicated the female homogametic XX/XY sex determination system in P. ussuriensis. The optimization of a protocol for the successful induction of meiogynogenesis in the bagrid catfish lays the basis for all‐male production and is useful in ascertaining the genetic sex determination system in this promising aquaculture species.     

低盐胁迫下松江鲈HSPB1、HSPB7和HSPB11基因的表达变化规律

为了探究小分子热休克蛋白基因HSPB1、HSPB7和HSPB11在松江鲈(Trachidermus fasciatus)应对低盐胁迫过程中的调节作用,本研究基于前期转录组数据,获取3个目标基因的序列信息并进行了系统进化分析,利用实时荧光定量PCR技术检测了3个基因在两种低盐胁迫处理下不同时间点(0 h、12 h、24 h和48 h)在鳃、肠、肾和肝组织中的表达水平。系统进化分析结果表明, HSPB1、HSPB7和HSPB11基因分别聚类形成独立分支;在各基因分支中,松江鲈与已报道的鲈形目、鲤形目和鳉形目等鱼种共同聚为硬骨鱼类分支。在两种低盐胁迫处理下, 3个基因在鳃组织中的表达量均在12h显著升高,而在肠、肾和肝组织中的表达量则呈现不同的变化趋势。肠组织中,HSPB7和HSPB11在盐度渐变低盐胁迫(盐度变化速率1.1/h)下表达量均显著升高, HSPB1表达量在48 h显著降低;盐度骤变低盐胁迫(盐度变化速率27/h)下HSPB1和HSPB7表达量在24 h显著升高, HSPB11表达量显著降低。肾组织中,HSPB1、HSPB7和HSPB11表达量均仅在盐度渐变低盐胁迫24h显著升高;盐度骤变低盐胁迫下HSPB1表达量显著降低, HSPB7和HSPB11表达量则显著升高。肝组织中, HSPB7无表达; HSPB1表达量在盐度渐变低盐胁迫下无显著变化,但在盐度骤变低盐胁迫下则显著升高;HSPB11表达量在两种处理下均显著升高。本研究比较分析了HSPB1、HSPB7和HSPB11基因在松江鲈应对不同低盐胁迫时表达变化规律的异同,相关结果为探讨小分子热休克蛋白在鱼类应激调节过程中的作用及洄游性鱼类适应盐度变化的分子调控机制提供了理论依据。