Recruitment of Nox4 to a Plasma Membrane Scaffold Is Required for Localized Reactive Oxygen Species Generation and Sustained Src Activation in Response to Insulin-like Growth Factor-I

Nox4-derived ROS is increased in response to hyperglycemia and is required for IGF-I-stimulated Src activation. This study was undertaken to determine the mechanism by which Nox4 mediates sustained Src activation. IGF-I stimulated sustained Src activation, which occurred primarily on the SHPS-1 scaffold protein. In vitro oxidation experiments indicated that Nox4-derived ROS was able to oxidize Src when they are in close proximity, and Src oxidation leads to its activation. Therefore we hypothesized that Nox4 recruitment to the plasma membrane scaffold SHPS-1 allowed localized ROS generation to mediate sustained Src oxidation and activation. To determine the mechanism of Nox4 recruitment, we analyzed the role of Grb2, a component of the SHPS-1 signaling complex. We determined that Nox4 Tyr-491 was phosphorylated after IGF-I stimulation and was responsible for Nox4 binding to the SH2 domain of Grb2. Overexpression of a Nox4 mutant, Y491F, prevented Nox4/Grb2 association. Importantly, it also prevented Nox4 recruitment to SHPS-1. The role of Grb2 was confirmed using a Pyk2 Y881F mutant, which blocked Grb2 recruitment to SHPS-1. Cells expressing this mutant had impaired Nox4 recruitment to SHPS-1. IGF-I-stimulated downstream signaling and biological actions were also significantly impaired in Nox4 Y491F-overexpressing cells. Disruption of Nox4 recruitment to SHPS-1 in aorta from diabetic mice inhibited IGF-I-stimulated Src oxidation and activation as well as cell proliferation. These findings provide insight into the mechanism by which localized Nox4-derived ROS regulates the sustained activity of a tyrosine kinase that is critical for mediating signal transduction and biological actions.     

Dissipative particle dynamics simulation of a gold nanoparticle system

Dissipative particle dynamics (DPD) was carried out to study systems containing gold atoms, organic ether (oligohydroquinonyl ether terminated with a thiol group) and organic solvents. The components in the simulated system are very different in size and chemical nature. Our simulation showed that the reproduction of the macroscopic experimental phase separation, properly dividing the polymeric molecule into beads, selecting the size of gold bead, and choosing the appropriate interaction parameters between beads are crucial. In addition, the solvent effect was the dominant factor for the formation of spherical aggregates of Au atoms and organic ether molecules. We report the interaction strengths between the solvent and gold clusters. Our work has demonstrated that DPD methods can be applied to the study of complex meso-scale systems.     

家兔三叉神经终止核对颏舌肌肌电活动的调制作用

本工作在35只氨基甲酸乙酯麻醉、自主呼吸的家兔上观察了刺激三叉神经终止核(NTV)对颏舌肌肌电活动的影响。结果发现,电刺激NTV和NTV内微量注射谷氨酸钠都能使颏舌肌出现明显的易化效应。电刺激NTV背侧与腹侧时,颏舌肌肌电反应的潜伏期分别为5.9±0.7ms和3.0±0.4ms,电刺激舌下神经核时颏舌肌反应的潜伏期为2.2±0.2ms。结果提示三叉神经终止核的兴奋可加强颏舌肌的活动从而减小上呼吸道阻力。     

Evaluation of housekeeping genes as references for quantitative real-time PCR analysis of European eel,Anguilla anguilla

Eels are important aquaculture species for which an increasing number of reference genes are being identified and applied. In this study, five housekeeping genes [RPL7 (ribosomal protein L7), 18 S (18 S ribosomal RNA), EF1A (elongation factor 1α), ACTB (β-actin) and GAPDH (glyceraldehyde-3-phosphate dehydrogenase)] were chosen to evaluate their reliability as reference genes for quantitative real-time PCR (qPCR) for the study of Anguilla anguilla. The expression of the selected genes in different eel tissues was determined using qPCR at different growth stages or upon challenge by Anguillid herpesvirus (AngHV), and the expression levels of these genes were then compared and evaluated using the geNorm and NormFinder algorithms. Then, RefFinder was used to comprehensively rank the examined housekeeping genes. Interestingly, the expression of the evaluated housekeeping genes exhibited tissue-dependent and treatment-dependent variations. In different growth periods A. anguilla tissues, the most stable genes were the following: ACTB in mucus; 18 S in skin and kidney; RPL7 in muscle, gill, intestine and brain; EF1A in heart and liver; and GAPDH in spleen. In contrast, in AngHV-challenged A. anguilla tissues, the most stable genes were the following: 18 S in mucus; RPL7 in skin, gill, heart, spleen, kidney and intestine; EF1A in muscle and liver; and ACTB in brain. Further comparison analysis indicated that the expression of RPL7 and EF1A was stable in multiple A. anguilla tissues in different growth periods and in eels challenged by AngHV. Nonetheless, the expression level of GAPDH in eel tissues was lower, and it was unstable in several tissues. These results indicated that the selection of reference genes for qPCR analysis in A. anguilla should be made in accordance with experimental parameters, and both RPL7 and EF1A could be used as reference genes for qPCR study of A. anguilla at different growth stages or upon challenge by AngHV. The reference genes identified in this study could improve the accuracy of qPCR data and facilitate further studies aimed at understanding the biology of eels.     

Terpenoids and Their Possible Role in Defense Against a Fungal Pathogen Alternaria tenuissima in Chrysanthemum morifolium Cultivars

Journal of Plant Growth Regulation - Terpenoids are a class of structurally diverse natural products involved in various plant biological processes. Their primary function is believed to provide...     

单增李斯特菌胎盘感染的体内外模型研究进展

单核细胞增生李斯特氏菌（Listeria monocytogenes）是重要的食源性致病菌,能引发人类的李斯特菌病,是全球公共卫生问题之一。该菌易感染孕妇,引起胎儿和新生儿的侵袭性李斯特菌病,严重威胁母婴健康。因此,建立有效的单增李斯特菌感染胎盘体内外模型,解析和探究单增李斯特菌经胎盘感染机制,是预防和控制单增李斯特菌感染母婴的关键所在。本文综述了可用于研究单增李斯特菌母婴感染的体内外胎盘模型,总结和讨论了各类模型的优势和局限性;并着重分析了体外三维胎盘屏障模型在单增李斯特菌感染方面的研究进展和未来研究方向。以期为深入解析该菌经胎盘感染的途径、发病机制提供支持,并为预防和控制母婴李斯特菌病提供科学参考。     

有机物料对喀斯特地区石灰土有效N、Fe、Zn含量的影响

为研究不同有机物料对喀斯特石灰土元素有效性的影响,采用40 d的室内培养实验,比较了单独添加不同比例（1%、3%、5%）的生物质炭、鸡粪肥、羊粪肥对喀斯特石灰土有效N、Fe、Zn含量的影响。结果表明：添加生物质炭提高了喀斯特石灰土的pH值,而添加鸡粪肥和羊粪肥降低了喀斯特石灰土的pH值;添加3种有机物料均增加了喀斯特石灰土的有机质含量,大小关系为：生物质炭 > 鸡粪肥 > 羊粪肥,但添加鸡粪肥和羊粪肥土壤有机质的化学活性和微生物活性更高。受pH、有机质活性、碳氮比等因素的影响,添加鸡粪肥和羊粪肥能增加土壤有效N含量,但两种有机肥对土壤有效N的提高效果相差不大,而添加生物质炭反而降低了土壤有效N的含量;3种有机物料均能提高土壤的有效Fe和有效Zn含量,其中鸡粪肥效果最佳,其次为羊粪肥和生物质炭。当3种有机物料的添加比例为5%时,生物质炭处理土壤的有效N、Fe、Zn含量分别是对照处理的0.92、1.13、1.21倍;鸡粪肥处理土壤的有效N、Fe、Zn含量分别是对照处理的1.22、1.63和3.39倍;羊粪肥处理土壤的有效N、Fe、Zn含量分别是对照处理的1.27、1.34和2.59倍。所以,相对于生物质炭,有机粪肥对喀斯特地区的石灰土有更好的改良效果。     

一株产β-葡萄糖苷酶甘草内生菌的筛选、全基因组分析及产酶优化

【背景】从健康甘草须根中分离获得的一株芽孢杆菌具有高产β-葡萄糖苷酶的活性。【目的】探究分离菌株潜在的产酶遗传信息,为该菌深入研究与工业应用提供数据支撑。【方法】利用七叶苷培养基进行产β-葡萄糖苷酶的益生菌筛选,筛到一株产β-葡萄糖苷酶的芽孢杆菌,采用三代Nanopore PromethION和二代Illumina NovaSeq平台对菌株进行基因组测序与组装、并通过基因预测与功能注释等生物信息分析预测菌株潜在的β-葡萄糖苷酶基因。另外,以β-葡萄糖苷酶活性为指标,研究碳源、氮源、接种量、温度和起始pH对菌株产酶活性的影响。【结果】从甘草须根中分离得到一株具有β-葡萄糖苷酶活性的菌株,通过形态学观察、生理生化和分子生物学试验鉴定为芽孢杆菌属菌株,并命名为Bacillus rugosus A78.1。该菌株基因组大小为4 146 938 bp,G+C含量为43.86%,共编码4 255个基因。在基因组中,共注释到碳水化合物活性酶基因192个,其中β-葡萄糖苷酶基因10个,分别属于GH1和GH3家族基因。在基因本体（GO）、京都基因与基因组百科全书（Kyoto encyclopedia of genes and genomes,KEGG）和同源基因簇（clusters of orthologous groups of proteins,COG）数据库分别注释到2 896、4 019和3 657个基因。该菌株基因组测序结果上传至NCBI获得GenBank登录号为CP096590。菌株A78.1产β-葡萄糖苷酶的最佳碳、氮源分别为0.5%葡萄糖、1.0%酵母浸粉,最佳培养条件为温度37℃、3%接种量、pH 6.0,此条件下β-葡萄糖苷酶活力可达到（5.640±0.085） U/mL。【结论】通过全基因组测序分析及产酶优化试验确定了Bacillus rugosus A78.1优良的产β-葡萄糖苷酶能力及在碳水化合物代谢方面的潜力,为该菌株在纤维素分解、糖苷类化合物水解等生物、化工和食品领域的研究与应用提供基础。     

不同生境银柴胡根内生菌群落特征及其与药材主要有效成分、产量的相关性分析

【背景】银柴胡（Stellaria dichotoma var.lanceolata）具有重要的临床药用价值,其总甾醇和总黄酮含量是评价药材的关键。【目的】探究药用植物银柴胡在不同生境下根内生菌群落特征及其与药材主要成分、产量之间的关系。【方法】采用高通量测序技术和药材常规测定方法,分析了风沙土（semi-fixed aeolian sandy soil,SFA）生境、石砾质土（lithosol,LI）生境和黄绵土（loessal,LO）生境银柴胡根内生菌群落特征及其与药材性状响应关系。【结果】各生境银柴胡内生优势细菌门为放线菌门（Actinobacteriota）和变形菌门（Proteobacteria）,优势真菌门为子囊菌门（Ascomycota）和担子菌门（Basidiomycota）,而内生优势菌属因生境不同各不相同;银柴胡药材主要有效成分总甾醇和总黄酮含量在LI生境中较高,而单株干重和干鲜比在SFA生境中较高。Spearman相关性分析表明,与银柴胡药材有效成分及产量显著正相关的内生菌相对较多。综合比较,内生细菌如metagenome_g__norank_f__67-14和内生真菌如unclassified_p__Ascomycota等更为显著。【结论】与银柴胡药材关键活性成分相关的内生菌群落在种类鉴定和提取、菌种培养和次生代谢物分析等方面具有广阔的研究价值。本研究为银柴胡道地产区药材高质量产业发展提供理论参考。