花生荚果发育及其调控研究进展

花生是重要的油料与经济作物,在农业种植业结构调整中发挥重要作用。荚果是花生的收获器官,深入 研究花生荚果发育及其调控,可以为高产育种提供理论依据。本文从花生荚果发育过程和内外限制因素的调控作 用,并结合激素、营养元素、遗传学研究以及DNA、RNA等分子调控机制,综述了近年来花生荚果发育相关的研究进 展,为后续研究提供参考。     

Effects of calpain-2 and autophagy-related protein 5 on hepatocyte apoptosis induced by endoplasmic reticulum stress

AIMTo investigate the effects of calpain-2 and autophagy-related protein 5 (Atg5) on apoptosis of BRL-3A rat normal liver cells during endoplasmic reticulum stress (ERS) induced by dithiothreitol (DTT). METH?ODS: BRL-3A cells were treated with DTT at 2.0 mmol/L for 0, 6, 12 and 24 h to induce ERS. Real-time cell analysis (RTCA) was used to measure the effect of DTT on BRL-3A cell proliferation. Apoptosis and cell cycle distribution were analyzed by flow cytometry. The mRNA expression of calpain-2 and Atg5 was detected by real-time PCR. The protein levels of calpain-2, Atg5, Atg7, Atg12 and microtubule-associated protein 1 light chain 3 (LC3) were determined by Western blot. The interaction between calpain-2 and Atg5 was investigated by co-immunoprecipitation (Co-IP). RESULTSThe proliferation of BRL-3A cells treated with DTT was significantly inhibited. The apoptosis of BRL-3A cells was significantly increased after DTT treatment for 6, 12 and 24 h as compared with 0 h group (P<0.05). The cell cycle was arrested in G₁ phase after DTT treatment (P<0.05). After DTT treatment for 6, 12 and 24 h, the mRNA expression of calpain-2 and Atg5 in the BRL-3A cells was significantly increased as compared with 0 h group (P<0.05). The protein levels of calpain-2, Atg12 and Atg7 in the cells treated with DTT for 6, 12 and 24 h were significantly higher than those in 0 h group, and the ratio of LC3-II/LC3-I was also significantly higher than that in 0 h group, while Atg5 expression was significantly lower than that in 0 h group (P<0.05). The results of Co-IP found that the anti-calpain-2 antibody precipitated Atg5 protein from the cell lysates, and the anti-Atg5 antibody also precipitated calpain-2 from the cell lysates, which confirmed the interaction between calpain-2 and Atg5. CONCLUSION Calpain-2 may participate in ERS-induced hepatocyte apoptosis by interacting with Atg5.     

Sulodexide protects against hyperglycemia-induced retinal vascular injury via suppressing NOX4/NLRP3 pathway

AIM To investigate the effect of sulodexide (SDX) on high glucose-induced damage in retinal microvascular endothelial cells. METHODS (1) High-fat diet combined with intraperitoneal injection of streptozocin were used to induce type 2 diabetes mellitus (DM) followed by injection of saline or SDX in C57BL/6J male mice. Retinal microvascular leakage and density, and the protein levels of NLRP3 inflammasome-related proteins, zonula occludens-1 (ZO-1) and NADPH oxidase 4 (NOX4) were measured. (2) Human retinal microvascular endothelial cells (HRMECs) were treated with normal glucose or high glucose with or without SDX, and were further transfected with siRNA to knock down NOX4, or infected by adenovirus to over-express NOX4. The protein levels of ZO-1, VE-cadherin (VE-Cad), NOX4 and NLRP3 inflammasome-related proteins as well as the level of reactive oxygen species (ROS) were detected. RESULTS Treatment with SDX increased the protein level of ZO-1, attenuated retinal leakage and NLRP3 inflammasome activation, and enhanced the density of microvasculature and the number of ganglion cells in diabetic retinas. The protein levels of ZO-1 and VE-Cad were decreased, while the levels of NOX4, NLRP3 inflammasome-related proteins and ROS generation were increased in high glucose-treated HRMECs. Silencing of NOX4 inhibited high glucose-induced increases in NLRP3 inflammasome and ROS generation, and decreases in the protein levels of ZO-1 and VE-Cad. Over-expression of NOX4 significantly increased the levels of NLRP3 inflammasome-related proteins and ROS generation in HRMECs, and reduced the protein levels of ZO-1 and VE-Cad. Treatment with SDX partly reversed NOX4 over-expression-induced changes. CONCLUSION SDX alleviates hyperglycemia-induced retinal microvascular endothelial injury via inhibiting NOX4/ROS/NLRP3 pathways.     

Mechanism of elemene enhancing radiosensitivity of human glioma U251 cells

AIM To investigate the effect of elemene on the radiosensitivity of human glioma U251 cells and its mechanism. METHODS The U251 cells were used as a glioma model in vitro, and were exposed to different concentrations of elemene and different doses of radiation. The cell viability was measured by MTT assay, the apoptosis and cell cycle distribution were analyzed by flow cytometry, and the related protein levels were determined by Western blot. RESULTS Elemene inhibited the viability of U251 cells in vitro and enhanced the radiosensitivity of the cells. The cells in radiotherapy combined with elemene group had higher rates of early apoptosis, secondary necrosis and total cell death than those in radiation group. Elemene induced G₂/M phase arrest in the U251 cells. Elemene reduced the protein expression of cell division cycle protein 2 （Cdc2）, which resulted in the decrease in cyclin B1 expression induced by radiotherapy, thereby inhibiting the formation of cyclin B-Cdc2 complex. Elemene reduced Cdc2 activity by inhibiting the phosphorylation of Cdc2 protein at threonine 161, thereby inducing G₂/M phase arrest in the cells. It also mediated apoptosis by down-regulating survivin expression. CONCLUSION Elemene may increase the sensitivity of U251 cells to radiotherapy by down-regulating Cdc2 protein, decreasing cyclin B1 expression, inhibiting the formation of cylcin B-Cdc2 complex and down-regulating the expression of survivin.     

CD36/Src/ERK pathway is involved in process of monocyte differentiation into macrophages

AIM To investigate the role of fatty acid translocase (FAT/CD36) on differentiation of monocytes to macrophages. METHODS Human monocyte THP-1 cells were treated with phorbol 12-myristate 13-acetate (PMA) at 0, 100 and 200 μg /L. Small interfering RNA (siRNA) targeting CD36 (siCD36) was employed to knock down the expression of CD36 in THP-1 cells. The CD36 over-expression (CD36OE) cell line was constructed by transfection with a recombinant lentivirus containing CD36 cDNA. Optical microscopy and crystal violet staining were used to detect the monocyte morphological changes and adhesion ability. The protein expression of CD36 was measured by flow cytometry and Western blot. The mRNA levels of CD36, CD11b and CD80 were detected by real-time PCR. The protein levels of extracellular signal-regulated kinase (ERK） and Src tyrosine kinase were determined by Western blot. RESULTS The cellular adhesiveness of THP-1 cells was elevated in the process of monocytes differentiation, and the expression of CD36 was increased in this process as well (P<0.01). siCD36 was transfected into the THP-1 cells (CD36i group) and the silencing efficiency was approximately 80%. The cell surface area and cellular adhesiveness were significantly decreased in CD36i group compared with scrambled siRNA (NCi) group (P<0.01). The mRNA levels of CD11b and CD80 were decreased in CD36i group compared with NCi group (P<0.01). The cell surface area and cellular adhesiveness were increased in CD36OE group compared with empty vector (vector) group (P<0.05). The mRNA levels of CD11b and CD80 were increased in CD36OE group compared with vector group (P<0.01). The phosphorylation levels of ERK and Src were decreased in CD36i group compared with NCi group (P<0.05). CONCLUSION CD36 promotes the differentiation of human monocyte THP-1 cells to macrophages by increasing the phosphorylation of Src and further activating ERK.     

硅藻土对5种储粮害虫和不同磷化氢抗性水平杂拟谷盗防治效果的研究

为初步了解硅藻土对储粮害虫的防治效果以及与害虫磷化氢抗性发生发展的关系, 本研究采用直接拌粮法(设置剂量梯度为0?0.2?0.4?0.6 g/kg和 0.8 g/kg)测定硅藻土对赤拟谷盗?杂拟谷盗?锈赤扁谷盗?谷蠹?玉米象的防治效果, 以及磷化氢抗性杂拟谷盗(抗性倍数为 2.3~144.7)对硅藻土的敏感性差异; 除此之外, 本研究还分析了0.4 g/kg硅藻土在 4 种粮食(小麦?玉米?大豆?稻谷)中对赤拟谷盗的杀虫效果?研究结果表明:一定剂量(0.2~0.8 g/kg)的硅藻土均能够在一定时间内有效杀死上述 5种储粮害虫, 不同储粮害虫对硅藻土的敏感性存在显著差异(P<0.05), 其中杂拟谷盗对硅藻土的耐受性最强, 玉米象对硅藻土最为敏感?除个别品系外, 不同磷化氢抗性品系的杂拟谷盗对硅藻土的敏感性不存在显著差异(P>0.05), 且与磷化氢抗性无关; 硅藻土在不同粮食中对害虫的作用效果存在显著性差异(P<0.05)(处理 7 d后, 死亡率为 13%~98%), 其中在大豆中对赤拟谷盗的杀虫效果最强, 在玉米中对其作用效果不明显?因此本研究得出结论:硅藻土对主要储粮害虫均具有一定的防治作用, 且对抗磷化氢的杂拟谷盗具有良好的致死效果?因此, 硅藻土具备成为储粮害虫防治及其磷化氢抗性治理药剂的潜力?     

基于主成分分析法的鸡汤与不同鸡肉酶解液中游离氨基酸的对比分析

为获得与鸡汤中组成成分差异性最小、风味类似的鸡肉蛋白酶解液,并为鸡肉香精制作提供理论依据和参考,选用6种蛋白酶(动物蛋白酶、复合蛋白酶、木瓜蛋白酶、碱性蛋白酶、风味蛋白酶和中性蛋白酶)对鸡肉进行酶解,检测鸡汤与不同鸡肉酶解液的组成成分与相对含量,分析17种游离氨基酸的呈味特性,并通过主成分分析法(principal component analysis, PCA)对比分析鸡汤与鸡肉酶解液中游离氨基酸组成的相似性与差异性。结果表明,动物蛋白酶对鸡肉酶解效果最好,水解度为19.21%;复合蛋白酶其次,水解度为18.52%。对比鸡汤及鸡肉酶解液组成成分发现,鸡汤中检测到33种物质,鸡肉酶解液中检测到36种物质,同时相对含量有差异。对比鸡汤与鸡肉酶解液中呈味氨基酸发现,复合蛋白酶酶解液中鲜味氨基酸与鸡汤中相对含量相近,为10.95%,且谷氨酸与天冬氨酸相对含量与鸡汤相比差异不显著。通过PCA对比发现,复合蛋白酶酶解的鸡肉酶解液中游离氨基酸种类和相对含量与鸡汤差异最小,同时呈味特性类似,具有相似的滋味。     

施肥对春青稞干物质积累、分配及产量的影响

为研究施肥对青稞干物质积累、分配及产量的调节作用,以‘藏青27’、‘QTB13’和‘QTB25’为试验材料,比较分析不同施肥处理下干物质积累、分配及产量的变化规律。结果表明：增加施肥量促进青稞分蘖期—成熟期的干物质积累及开花期和成熟期干物质向营养器官和籽粒的分配,提高了花前营养器官贮藏同化物转运量及对籽粒贡献率,降低了花后同化物输入籽粒量对籽粒贡献率。‘QTB13’和‘QTB25’在F₂条件下,更有利于干物质积累及向营养器官和穗部的分配,花后同化物输入籽粒量最大,产量也最大。‘藏青27’在F₃条件下,更有利于干物质积累及向营养器官和穗部的分配,花后同化物输入籽粒量和对籽粒贡献率最大,产量也最大。说明合理施肥有利于青稞干物质积累分配及产量提高。     

运用植被指数时序特征对落叶松人工林分类

为探究植被指数时序特征是否有利于落叶松人工林提取,以孟家岗林场为研究试验区域,根据落叶松人工林季相和物候特征,利用Landsat8OLI影像数据提取研究区内5种植被的归一化植被指数(I NDV)、差值植被指数(I DV)、比值植被指数(I RV)、增强型植被指数(I EV),构建相应的植被指数时序特征。采用最大似然和随机森林两种方法对单一时相影像和加入植被指数时序特征的影像进行对比试验。结果表明:影像中加入植被指数时序特征后,最大似然算法的分类总体精度为89.53%,Kappa系数为0.87,比单一时序特征的影像分类精度提高了13.35%;随机森林算法的森林类型分类总体精度为93.22%,Kappa系数为0.92,比单一时序特征的影像分类精度提高了19.8%。因此,加入植被指数时序特征后能得到更高的落叶松人工林提取精度。     

鸭坦布苏病毒病、鸭圆环病毒病与鸭疫里默氏杆菌混合感染的诊断

为确诊贵州省三穗县某鸭场62日龄花边鸭发病原因,通过临床症状观察及对采集的10只病鸭进行病理剖检、细菌分离鉴定和病毒PCR/RT-PCR检测。结果表明:分离到4株鸭疫里默氏杆菌,对头孢类药物高度敏感,对大环内酯类和氨基糖苷类药物耐药;病毒特异性引物扩增出鸭坦布苏病毒和鸭圆环病毒条带。该鸭场病鸭由鸭坦布苏病毒、鸭圆环病毒和鸭疫里默氏杆菌混合感染所致。