基于黄土高原关键带类型的土地利用与年径流产沙关系空间分异研究

区域植被恢复改变了土地利用类型,从而有效控制了水土流失,但土地利用与水土流失关系的空间分异尚未明晰。整合了黄土高原坡面径流小区试验观测研究文献59篇和1121条年径流产沙记录,以8大关键带类型作为空间分层依据,采用地理探测器分析了土地利用与年径流产沙关系的空间分异。结果显示：撂荒地的年均径流量和产沙量最高分别为35.99 mm和4208.82 g/m²,撂荒地、裸地和耕地的产流产沙能力显著高于人工草地、林地、自然草地和灌丛,灌丛和林地的年均产沙量显著低于人工和自然草地（P<0.05）;除了撂荒地的年均产沙量在山地森林关键带最高（16240.40 g/m²）外,在丘陵沟壑农林草交错关键带的撂荒地年均径流产沙显著高于丘陵农业-草地关键带,丘陵沟壑农林草交错关键带和丘陵农业-草地关键带裸地、耕地的产流产沙能力较高,人工草地和灌丛年均产沙量显著高于其他关键带类型（P<0.05）;在山地森林关键带的林地年均径流量、径流系数和产沙量最低,分别为1.56 mm、0.41%和307.36 g/m²,而自然草地在各关键带类型都有较高的年均产流量和较低的年均产沙量;坡面径流小区的局地特征（如土地利用、面积、坡度、坡长）是影响年径流产沙关键带分异的首要因素,且存在多因子互作、非线性增强的关系。这些结果表明植被恢复能有效地保持水土,但是区域植被恢复时需要选择合适的类型,黄土丘陵沟壑区应首选自然草地、灌丛和林地。研究可为黄土高原区域植被恢复的优化配置提供科学依据。     

An alternative,low-cost method to chill water for critical thermal minima trials

Water temperature is an important abiotic factor that impacts physiological processes in fish. Attempts to quantify thermal tolerance of fishes exposed to various temperatures have been performed since the 1800s. A common approach to test the thermal tolerance of fishes is the critical thermal method. Traditionally this method has required access to large and expensive lab equipment. However, many individuals may not have direct access to such equipment, making critical thermal studies difficult-to-impossible to conduct. We present a simple and cost-friendly alternative device to use for critical thermal minima trials. This device uses a cooler with a copper line and copper coil to chill water within an aquarium. A pump and valves control the water flow as it passes from the aquarium through the copper. This allows the user to lower the water temperature in the aquarium from 28^oC to 0^oC at a steady rate of 0.23^oC min⁻¹. The device allows those with limited funding or without access to traditional lab equipment the ability to perform critical thermal minima trials, expanding our collective understanding of life histories of fish and their potential vulnerabilities to increasingly altered thermal environments.     

集束化管理模式在急诊危重患者院内转运的应用及效果评价

目的探讨集束化管理模式在急诊危重患者院内转运中的应用效果。方法选取2019年9月~2020年4月我院急诊科就诊的324例急诊危重患者为研究对象,按转运方式不同分为观察组和对照组各162例。观察组采用集束化管理模式转运危重患者,对照组采用传统模式转运危重患者,比较两组患者的院内转运时间、投诉率、转运意外发生率(包括病情变化、脱管、仪器故障等)及满意度(包括转运患者的满意度及接收科室医护人员的满意度)情况。结果观察组院内危重患者转运时间明显短于对照组(P<0.05),转运患者的投诉率、及转运意外发生率均低于对照组(均P<0.05);观察组转运患者的满意度、接收科室医护人员的满意度均明显高于对照组,差异均有统计学意义(均P<0.05)。结论集束化管理模式在急诊危重患者院内转运中可缩短患者转运时间,降低不良事件发生率,提高了患者及接收科室医护人员的满意度。     

The influence of flume length and group size on swimming performance in shortnose sturgeon Acipenser brevirostrum

The main objectives of this study were to determine optimal methodologies to assess the general swimming performance of juvenile shortnose sturgeon Acipenser brevirostrum. Swimming densities (group v. individual swimming) and flume length (2 v. 1 m) were altered to verify if any of those variables affected performance (i.e. time to fatigue) during critical swimming (U(crit)) and endurance tests. Results for both U(crit) and endurance swimming were not significantly different between fish swum in groups of five or fish swum individually. The U(crit) values, however, were c. 22% higher for fish swum in a longer flume. Although swimming fish in groups did not improve swimming performance, group swimming lowered the variance of the data. Results also reveal that juvenile A. brevirostrum may not possess an ability to swim at high speeds (i.e. burst phase) for long periods.     

Limited expression of reticulocalbin-1 in lymphatic endothelial cells in lung tumor but not in normal lung

Lymphatic endothelial cells in tumors (T-LECs) are considered to have different characteristics from LECs in non-tumor tissues (N-LECs). However, differences between the two types have not been well analyzed at molecular level. In this report, we performed differential proteome analysis of T-LEC and N-LEC models prepared by cultivation of LECs in tumor conditioned medium. By expression profiling of identified proteins using tissue microarrays, reticulocalbin-1 was found to be expressed in clinical specimen-derived T-LECs and lung cancer cells but not N-LECs. It is suggested that reticulocalbin-1 may be an important molecule in understanding T-LEC function and control of lymphatic metastasis.     

暗培养对黄瓜子叶节再生频率及其相关酶活性和可溶性蛋白含量的影响

以黄瓜品种新泰密刺子叶节为材料,观测了暗培养1~5 d黄瓜子叶节植株再生频率及其诱导过程中POD、SOD活性和可溶性蛋白含量的变化,以探究暗培养条件下黄瓜子叶节POD、SOD活性、可溶性蛋白含量与再生频率间的关系.结果表明,暗培养不仅可以使黄瓜子叶节POD活性持续增长,还有助于其活性保持在较高水平,D4处理在培养的第6天POD值高达243 U?g-1FW,对应的再生频率为87.20%,而对照的最高峰值仅为187.7 U?g-1FW,再生频率只有36.60%;POD的变化体现了各处理生理状态的差异,且各处理暗培养结束时的POD活性水平和POD峰值分别与植株再生频率之间存在显著正相关性,相关系数分别达到了0.921和0.839;而SOD活性水平与再生频率间无显著相关性;可溶性蛋白含量虽然可以体现子叶节生理状态的变化,但无法反映各暗处理对再生频率的影响差别.可见,暗培养有助于提高诱导过程中黄瓜子叶节POD活性的增速,使其活性保持在较高水平,且以POD活性为指标可以反映暗培养处理的有效性.     

Frequent mutations in NOTCH1 ligand-binding regions in Japanese oral squamous cell carcinoma

Recent studies showed that head and neck squamous cell carcinoma (HNSCC) including oral squamous cell carcinoma (OSCC) of Caucasian, Chinese and Indian patients frequently have NOTCH1 mutations. We found eight of 84 OSCC in Japanese patients have point mutations (9.5%) correspond to the ligand binding region of NOTCH1 protein. Two set of them are the same mutations and all mutations are non-synonymous G > A transitions. In addition, median disease-free survival is significantly longer in patients with NOTCH1-mutated tumors as compared to those without the mutation (P < 0.05). The protein structure simulation based on X-ray crystallography indicated that new p.A465T mutation leads to a conformational change of NOTCH1 ligand binding domain as well as the p.G481S mutant NOTCH1 with a loss of flexibility around this residue. These results suggest that NOTCH1 mutation occurs frequently in Japanese OSCC in the vicinity of the ligand binding region and, these mutations cause downregulation of the NOTCH1 function.     

A survey of detergents for the purification of stable,active human cystic fibrosis transmembrane conductance regulator (CFTR)

Structural knowledge of the cystic fibrosis transmembrane conductance regulator (CFTR) requires developing methods to purify and stabilize this aggregation-prone membrane protein above 1 mg/ml. Starting with green fluorescent protein- and epitope-tagged human CFTR produced in mammalian cells known to properly fold and process CFTR, we devised a rapid tandem affinity purification scheme to minimize CFTR exposure to detergent in order to preserve its ATPase function. We compared a panel of detergents, including widely used detergents (maltosides, neopentyl glycols (MNG), C₁₂E₈, lysolipids, Chaps) and innovative detergents (branched alkylmaltosides, facial amphiphiles) for CFTR purification, function, monodispersity and stability. ATPase activity after reconstitution into proteoliposomes was 2–3 times higher when CFTR was purified using facial amphiphiles. ATPase activity was also demonstrated in purified CFTR samples without detergent removal using a novel lipid supplementation assay. By electron microscopy, negatively stained CFTR samples were monodisperse at low concentration, and size exclusion chromatography showed a predominance of monomer even after CFTR concentration above 1 mg/ml. Rates of CFTR aggregation quantified in an electrophoretic mobility shift assay showed that detergents which best preserved reconstituted ATPase activity also supported the greatest stability, with CFTR monomer half-lives of 6–9 days in MNG or Chaps, and 12–17 days in facial amphiphile. Cryoelectron microscopy of concentrated CFTR in MNG or facial amphiphile confirmed mostly monomeric protein, producing low resolution reconstructions in conformity with similar proteins. These protocols can be used to generate samples of pure, functional, stable CFTR at concentrations amenable to biophysical characterization.     

Induction of microRNA-138 by pro-inflammatory cytokines causes endothelial cell dysfunction

Exposure to pro-inflammatory cytokines, such as Angiotensin II, endothelin-1 or TNF leads to endothelial dysfunction, characterized by the reduced production of nitric oxide via endothelial nitric oxide synthase (eNOS). We recently identified the Ca²⁺ binding protein S100A1 as an essential factor required for eNOS activity. Here we report that pro-inflammatory cytokines down-regulate expression of S100A1 in primary human microvascular endothelial cells (HMVECs) via induction of microRNA-138 (miR-138), in a manner that depends on the stabilization of HIF1-α. We show that loss of S100A1 in ECs reduces stimulus-induced NO production, which can be prevented by inhibition of miR-138. Our study suggests that targeting miR-138 might be beneficial for the treatment of cardiovascular disease.     

Different activities of the conserved lysine residues in the double-stranded RNA binding domains of RNA helicase A in vitro and in the cell

Background

RNA helicase A regulates a variety of RNA metabolism processes including HIV-1 replication and contains two double-stranded RNA binding domains (dsRBD1 and dsRBD2) at the N-terminus. Each dsRBD contains two invariant lysine residues critical for the binding of isolated dsRBDs to RNA. However, the role of these conserved lysine residues was not tested in the context of enzymatically active full-length RNA helicase A either in vitro or in the cells.

Methods

The conserved lysine residues in each or both of dsRBDs were substituted by alanine in the context of full-length RNA helicase A. The mutant RNA helicase A was purified from mammalian cells. The effects of these mutations were assessed either in vitro upon RNA binding and unwinding or in the cell during HIV-1 production upon RNA helicase A–RNA interaction and RNA helicase A-stimulated viral RNA processes.

Results

Unexpectedly, the substitution of the lysine residues by alanine in either or both of dsRBDs does not prevent purified full-length RNA helicase A from binding and unwinding duplex RNA in vitro. However, these mutations efficiently inhibit RNA helicase A-stimulated HIV-1 RNA metabolism including the accumulation of viral mRNA and tRNA^Lys3 annealing to viral RNA. Furthermore, these mutations do not prevent RNA helicase A from binding to HIV-1 RNA in vitro as well, but dramatically reduce RNA helicase A–HIV-1 RNA interaction in the cells.

Conclusions

The conserved lysine residues of dsRBDs play critical roles in the promotion of HIV-1 production by RNA helicase A.

General significance

The conserved lysine residues of dsRBDs are key to the interaction of RNA helicase A with substrate RNA in the cell, but not in vitro.