不同强度火干扰下盘古林场天然落叶松林的空间结构

基于2011年7月大兴安岭外业调查数据以林隙为主要研究对象,选取景观生态学中斑块类型指数分析样地内林隙状况,并结合林木分布状态,分析不同强度林火干扰对天然落叶松林空间结构的影响。结果表明:在受中度林火干扰的林分内,只保留了少量的落叶松中径木、大径木,先锋树种在林分内呈现聚集分布;在未受林火干扰的林分和受林火轻微干扰的林分内,天然落叶松均呈现显著聚集分布;由于受到不同强度的林火干扰,林下区域与林隙区域出现不同程度的相互转化,林分空间结构发生了改变。林分按照所受林火干扰强度的递减,在同一时间不同空间上表现出了森林循环过程中所经历的林隙阶段状态、建立阶段状态、成熟阶段状态。     

我国城市人与自然耦合系统的协调度

城市作为人类生存与发展的主要空间载体,是人与自然耦合系统的典型代表。城市人与自然协调度是认识人与自然耦合机制重要内容,对揭示城市人类活动对生态环境的影响,指导城市建设具有重要意义。从水资源开发强度、土地开发强度、水资源供给能力、环境污染物排放强度与碳排放强度五个方面分析城市人与自然协调度特征,评估城市建设与发展对自然环境的影响程度,并评估了我国146个城市的协调度特征,进一步分析了城市人口规模、城市经济规模、城市社会发展水平、不同生态地理区人与自然耦合协调度的关系。结果表明：2016年城市平均协调度指数为87.90,不同城市的协调度差距很大且协调度与城市人口规模、经济规模、发展水平呈显著负相关,而六大生态地理区中,西南地区协调度最高,协调度指数为92.81,西北地区协调度最低,协调度指数为82.25。研究发现我国城市建设与发展对自然环境影响仍然较大,并表现为（1）我国城市发展总体仍处于高需求高排放的发展阶段;（2）生态环境承载力是影响城市人与自然耦合协调度的重要因素;（3）提高能源利用效率,降低碳排放强度在改善城市人与自然协调度中发挥作用。最后,从优化城市布局、提高水、能源利用效率、控制环境污染等方面提出政策建议,为评估城市生态文明建设与可持续发展提供参考与依据。     

呼吸机无创通气治疗急性心源性肺水肿临床研究

目的探讨大型多功能呼吸机及双相气道正压通气呼吸机治疗急性心源性肺水肿的临床价值。方法将48例急性心源性肺水肿患者分为无创通气治疗组（24例）和对照组（24例）,观察治疗前、后1h两组的血气分析及相关的症状、体征及病情缓解分值并进行统计学配对比较处理。结果治疗前各匹配组分析P〉0.05,说明两组基础病情具有可比性;治疗后1 h动脉血氧饱和度、血氧分压、呼吸频率、心率及缓解积分各组比较P〈0.01。结论表明治疗组较对照组的心肺功能改善更明显,由此表明该方法有极高的临床应用价值。     

Fatty acid-specific fluorescent probes and their use in resolving mixtures of unbound free fatty acids in equilibrium with albumin

We report the first measurements for profiling mixtures of unbound free fatty acids. Measurements utilized fluorescent probes with distinctly different response profiles for different free fatty acids (FFA). These probes were constructed by labeling site-specific mutants of the rat intestinal fatty acid binding protein (rI-FABP) with acrylodan. The probes were produced and screened by high-throughput methods, and from more than 30 000 such probes we selected six that together have sufficient specificity and sensitivity for resolving the profile of unbound FFA (FFAu) in mixtures of different FFAu. We developed analytical methods to determine the FFAu profile from the fluorescence (ratio) response of the different probes and used these methods to determine FFAu profiles for mixtures of arachidonate, linoleate, oleate, palmitate, and stearate in equilibrium with bovine serum albumin (BSA). Measurements were performed using mixtures with a range of total FFAu concentrations, including 0.9 nM, which is similar to normal plasma levels. We also measured single FFA binding isotherms for BSA and found that binding was described well by six to seven sites with the same binding constants (Kd). The Kd values for the FFA (4-38 nM) were inversely related to the aqueous solubility of the FFA. We constructed a model with these parameters to predict the FFAu profile in equilibrium with BSA and found excellent agreement between the profiles measured using the FFA probes and those calculated with this model. These results should lead to a better understanding of albumin's role in buffering FFAu and to profiling FFAu in intra- and extracellular biological fluids.     

B7H1-Ig fusion protein activates the CD4+ IFN-gamma receptor+ type 1 T regulatory subset through IFN-gamma-secreting Th1 cells

It has been demonstrated in our previous work that, in the human skin-grafting model, the expression of costimulatory molecule B7H1 (PD-L1) by keratinocytes plays an essential role in inducing local tolerance via activation of IL-10-secreting T cells. This study further analyzes the role of B7H1 in differentiation of type 1 T regulatory (Tr1) cells and explores underlying mechanisms. Mouse fusion protein B7H1-Ig is used, together with immobilized anti-CD3 mAb, to costimulate the purified naive CD4+ T cells. B7H1-Ig-treated CD4+ T cells were found to activate a characteristic Tr1 population possessing a CD4+ CD25- Foxp3- CD45RBlow phenotype. These regulatory T cells strongly inhibited the Th1-dominated MLR by secretion of IL-10 and TGF-beta. Moreover, B7H1-treated Tr1 cells also resulted in suppressed clinical scores and demyelination when adoptively transferred into mice with experimental allergic encephalomyelitis. Furthermore, analysis of the cytokine profile indicated that there were two differential reaction patterns during the B7H1-Ig-induced Tr1 development. These two patterns were characterized by activation of IFN-gammaR+ IL-10R- Th1 and IFN-gammaR+ IL-10R+ Tr1 cells, respectively. Secretion of IFN-gamma by Th1 and the expression of IFN-gammaR on Tr1 were critical for further Tr1 differentiation, as demonstrated by mAb blocking and by analysis in IFN-gamma(-/-) mice. In conclusion, B7H1 is capable of inducing Tr1 differentiation from naive CD4+ T cells by coactivation in an IFN-gamma- or Th1-dependent manner. Our study may shed some light upon the clinical usage of B7H1 as a therapeutic reagent for induction of tolerance.     

Form-Finding Model Shows How Cytoskeleton Network Stiffness Is Realized

In eukaryotic cells the actin-cytoskeletal network provides stiffness and the driving force that contributes to changes in cell shape and cell motility, but the elastic behavior of this network is not well understood. In this paper a two dimensional form-finding model is proposed to investigate the elasticity of the actin filament network. Utilizing an initially random array of actin filaments and actin-cross-linking proteins the form-finding model iterates until the random array is brought into a stable equilibrium configuration. With some care given to actin filament density and length, distance between host sites for cross-linkers, and overall domain size the resulting configurations from the form-finding model are found to be topologically similar to cytoskeletal networks in real cells. The resulting network may then be mechanically exercised to explore how the actin filaments deform and align under load and the sensitivity of the network’s stiffness to actin filament density, length, etc. Results of the model are consistent with the experimental literature, e.g. actin filaments tend to re-orient in the direction of stretching; and the filament relative density, filament length, and actin-cross-linking protein’s relative density, control the actin-network stiffness. The model provides a ready means of extension to more complicated domains and a three-dimensional form-finding model is under development as well as models studying the formation of actin bundles.     

Genetic diversity of <Emphasis Type="Italic">avenin-like b</Emphasis> genes in <Emphasis Type="Italic">Aegilops tauschii</Emphasis> Coss

Avenin-like storage proteins influence the rheological properties and processing quality in common wheat, and the discovery of new alleles will benefit wheat quality improvement. In this study, 13 avenin-like b alleles (TaALPb7D-A–M) were discovered in 108 Aegilops tauschii Coss. accessions. Ten alleles were reported for the first time, while the remaining three alleles were the same as alleles in other species. A total of 15 nucleotide changes were detected in the 13 alleles, resulting in only 11 amino acid changes because of synonymous mutations. Alleles TaALPb7D-E, TaALPb7D-G, and TaALPb7D-J encoded the same protein. These polymorphic sites existed in the N-terminus, Repetitive region (Left), Repetitive region (Right) and C-terminus domains, with no polymorphisms in the signal peptide sequence nor in those encoding the 18 conserved cysteine residues. Phylogenetic analysis divided the TaALPb7Ds into four clades. The Ae. tauschii alleles were distributed in all four clades, while the alleles derived from common wheat, TaALPb7D-G and TaALPb7D-C, belonged to clade III and IV, respectively. Alleles TaALPb7D-G and TaALPb7D-C were the most widely distributed, being present in nine and six countries, respectively. Iran and Turkey exhibited the highest genetic diversity with respect to TaALPb7D alleles, accessions from these countries carrying seven and six alleles, respectively, which implied that these countries were the centers of origin of the avenin-like b gene. The new alleles discovered and the phylogenetic analysis of avenin-like b genes will provide breeding materials and a theoretical basis for wheat quality improvement.     

A reliable and economical method for gaining mouse embryonic fibroblasts capable of preparing feeder layers

Mouse embryonic fibroblasts (MEFs) are widely used to prepare feeder layers for culturing embryonic stem cells (ESCs) or induced pluripotent stem cells (iPSCs) in vitro. Transportation lesions and exorbitant prices make the commercially obtained MEFs unsuitable for long term research. The aim of present study is to establish a method, which enables researchers to gain MEFs from mice and establish feeder layers by themselves in ordinary laboratories. MEFs were isolated from ICR mouse embryos at 12.5–17.5 day post-coitum (DPC) and cultured in vitro. At P2–P7, the cells were inactivated with mitomycin C or by X-ray irradiation. Then they were used to prepare feeder layers. The key factors of the whole protocol were analyzed to determine the optimal conditions for the method. The results revealed MEFs isolated at 12.5–13.5 DPC, and cultured to P3 were the best choice for feeder preparation, those P2 and P4–P5 MEFs were also suitable for the purpose. The P3–P5 MEFs treated with 10 μg/ml of mitomycin C for 3 h, or irradiated with X-ray at 1.5 Gy/min for 25 Gy were the most suitable feeder cells. Treating MEFs with 10 μg/ml of mitomycin C for 2.5 h, 15 μg/ml for 2.0 h, or irradiating the cells with 20 Gy of X-ray at 2.0 Gy/min could all serve as alternative methods for P3–P4 cells. Our study provides a reliable and economical way to obtain large amount of qualified MEFs for long term research of ESCs or iPSCs.     

小麦R2R3-MYB转录因子TaMYB3-4D的克隆及功能分析

MYB转录因子是植物最大的转录因子家族之一,广泛参与植物各种生理生化过程。该研究通过对小麦基因组测序数据库进行同源搜索,利用电子克隆技术从紫色籽粒小麦品种‘高原115’中分离得到了一个新的MYB基因TaMYB3-4 D。结果表明,TaMYB3-4D仅含有一个内含子,其编码蛋白含有2个连续的MYB结构域,为典型的R2R3-MYB蛋白。TaMYB3-4D系统发生关系上与调控花青素合成的MYB基因亲缘关系较近。TaMYB3-4 D与bHLH基因ZmR瞬时表达能够诱导白色胚芽鞘中花青素的合成。此外,TaMYB3-4 D基因仅在‘高原115’含花青素的种皮和胚芽鞘中表达,在根、茎、叶中均未表达。研究表明,TaMYB3-4 D基因是一个具有调控花青素合成代谢功能的R2R3-MYB基因,很有可能参与小麦花青素的生物合成。