Kinetic studies of electron transfer in the cyt b 5 : metHb system

 The kinetics of methemoglobin reduction by cytochrome b ₅ has been studied by stopped-flow and saturation transfer NMR. A forward rate constant k _f = 2.44×10⁴ M^–1 s^–1 and a reverse rate constant k _b = 540 M^–1s^–1 have been observed at 10 mm, pH 6.20, 25  °C. The ratio k _f/k _b = k _eq = 43.6 is in good agreement with the equilibrium constant calculated from the electrochemical potential between cyt b ₅ and methemoglobin. A bimolecular collisional mechanism is proposed for the electron transfer from cyt b ₅ to methemoglobin based on the kinetic data analysis. The dependence of the rate constants on ionic strengths supports such collisional mechanism. It is also found that the reaction rate strongly depends on the conformations of methemoglobin. Received: 20 February 1996 / Accepted: 4 June 1996     

Apigenin 7-glucoside diacetates in ligulate flowers of Matricaria chamomilla

From ligulate flowers of Matricaria chamomilla was isolated a mixture of apigenin 7-O-β-glucoside diacetates, which was shown to be based on (2″, 3″)- and (3″, 4″)-diacetates.     

微生物介导的金纳米颗粒合成

金纳米颗粒凭借其独特的光学和电化学特性,广泛应用于信息存储、化学传感、医学成像、药物传输以及生物标记等领域。近年来,生物法合成金纳米颗粒因其环境友好、绿色低毒等特点引起研究者的广泛关注。研究表明,多种微生物包括细菌、放线菌、真菌和病毒等均具有合成金纳米颗粒的能力。本文综述了微生物介导合成金纳米颗粒的特性、机制及应用,并对未来发展趋势进行了展望。     

Intravital lipid droplet labeling and imaging reveals the phenotypes and functions of individual macrophages in vivo

Macrophages play pivotal roles in the maintenance of tissue homeostasis. However, the reactivation of macrophages toward proinflammatory states correlates with a plethora of inflammatory diseases, including atherosclerosis, obesity, neurodegeneration, and bone marrow (BM) failure syndromes. The lack of methods to reveal macrophage phenotype and function in vivo impedes the translational research of these diseases. Here, we found that proinflammatory macrophages accumulate intracellular lipid droplets (LDs) relative to resting or noninflammatory macrophages both in vitro and in vivo, indicating that LD accumulation serves as a structural biomarker for macrophage phenotyping. To realize the staining and imaging of macrophage LDs in vivo, we developed a fluorescent fatty acid analog-loaded poly(lactic-co-glycolic acid) nanoparticle to label macrophages in mice with high efficiency and specificity. Using these novel nanoparticles, we achieved in situ functional identification of single macrophages in BM, liver, lung, and adipose tissues under conditions of acute or chronic inflammation. Moreover, with this intravital imaging platform, we further realized in vivo phenotyping of individual macrophages in the calvarial BM of mice under systemic inflammation. In conclusion, we established an efficient in vivo LD labeling and imaging system for single macrophage phenotyping, which will aid in the development of diagnostics and therapeutic monitoring. Moreover, this method also provides new avenues for the study of lipid trafficking and dynamics in vivo.Supplementary key words: macrophage, inflammation, lipid droplet, nanoparticle delivery, in vivo imaging, fatty acid analog, bone marrow, systemic inflammation, lipid trafficking, biomarker

Macrophages, a type of immune cells, almost reside in all tissues of body, from the skin to the bone marrow (BM) (1). Macrophages have remarkable plasticity, and they can be activated into specific subtypes by modifying their physiology and functions in response to local environmental cues. Activated macrophages are commonly divided into proinflammatory killing subtype and anti-inflammatory repairing subtype. Proinflammatory macrophages responding to bacteria, IFN-γ, and lipopolysaccharide (LPS) are involved in host defense and inflammation, whereas anti-inflammatory macrophages responding to interleukin-4 (IL-4), IL-10, and IL-13 play a pivotal role in tissue homeostasis and remodeling (2). Increasing evidence indicates that the reactivation of macrophages toward proinflammatory states under diverse kinds of stress is correlated with a plethora of inflammatory diseases, such as atherosclerosis, diabetes, obesity, rheumatoid arthritis, neurodegeneration, and BM failure syndromes (3, 4). Thus, characterization of macrophage activation status and the underlying molecular mechanism in situ will help elucidate their functions in these diseases; however, in vivo analysis of the macrophage activation status in their native multicellular microenvironment is challenging.Although lipid droplets (LDs) have been initially described as intracellular fat storage organelles in adipocytes, increasing studies indicate that myeloid cells also form LDs under inflammation and stress (5, 6). Macrophages, as the effector cells of innate immunity, are found to form LDs to support their host defense when exposed to pathogens, such as parasites, bacteria, and viruses (7, 8, 9, 10, 11). However, abnormal LD accumulation in tissue-resident macrophages correlates with the pathogenesis of various inflammatory diseases. For instance, foam cells in atherosclerotic lesions can maintain the local inflammatory response by secreting proinflammatory cytokines (12, 13, 14). Moreover, LD-accumulating microglia contribute to neurodegeneration by producing high levels of reactive oxygen species (ROS) and secreting proinflammatory cytokines (15). These findings indicate that LD accumulation might be a hallmark of macrophages with proinflammatory functions.In this study, based on the typical activation of in vitro BM-derived macrophages, we find that proinflammatory M_{(LPS + IFN-γ)} macrophages are characterized by LD accumulation, whereas resting macrophages and anti-inflammatory M_(IL-4) and M_(IL-10) macrophages do not contain any LDs. These features also hold for Matrigel plug-recruited macrophages and tissue-resident macrophages in mice. These findings demonstrate that LD accumulation could serve as a morphological index to distinguish proinflammatory macrophages from others.It is feasible to distinguish LD-containing cells using imaging techniques, which has translational potential for identification of proinflammatory macrophages in vivo. However, current techniques for LD visualization are traditional in vitro staining method, and in vivo staining and imaging of LD in individual macrophages remains a challenge. Through nanocarrier screening, we selected the poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs) as nanocarrier to deliver the lipophilic carbocyanine dye (DiI_C18(5) solid (1,1''-dioctadecyl-3,3,3'',3''-tetramethylindodicarbocyanine, 4-chlorobenzenesulfonate salt) [DiD]) and lipid staining dye (C1-BODIPY 500/510-C12) into macrophages. Using these dual fluorescence-labeled PLGA NPs, we achieved in situ and in vivo functional identification of single macrophages in various tissues under systemic or local inflammatory stress. Collectively, this study establishes an efficient in vivo labeling and imaging system of intracellular LDs for phenotyping the activation status and functions of individual macrophages in their dynamic niche, which is pivotal for disease diagnosis and preclinical research.     

基于遥感的建筑物高度快速提取研究综述

近年来我国城市化进程不断推进,不仅体现在城市面积上的增长,也体现在建筑物高度的增长。高度增长一方面能尽量克服城市土地资源匮乏的瓶颈,另一方面为优化城市结构及城市功能做出贡献。在城市遥感研究领域,对于城市建筑物高度的提取也成为研究的重点。城市建筑物高度的估计与测量,已成为城市规划和扩张、城市灾害风险预警与评估的重要参数,同时也为数字城市三维模型的建立提供了基础测绘资料。分别基于光学遥感影像、高分辨率SAR(Synthetic Aperture Radar)影像以及光学遥感影像与高分辨率SAR影像的融合三方面,全面阐述城市建筑物高度的提取方法,并比较两类影像在提取建筑物高度的优劣势,通过回顾早年研究方法,逐步引入近年来新的发展趋势。     

城市化进程中城市热岛景观格局演变的时空特征——以厦门市为例

热岛效应作为城市化过程中产生的特有环境问题,对其形成和演变规律的研究有助于人们提出有效的应对措施。以厦门市为研究对象,利用1987—2007年等时间间隔、同时相的5景Landsat TM/ETM+遥感影像数据进行地表温度反演,在此基础上使用景观格局指数分析厦门城市热岛景观格局随城市化进程演变的趋势。结果表明:随着厦门城市化进程加深,整个热岛景观在逐渐变得更加破碎化,高等级热岛景观斑块个数、类型面积和个体面积都增大;新的高等级热岛景观斑块都出现在原有高等级斑块附近,致使高等级类型的邻近度增加而各类型之间相互接触的程度也增加;景观总体的聚合度逐渐下降,而高等级热岛景观类型的聚合度则呈上升趋势;景观水平的蔓延度总体呈下降趋势,优势度高的低等级热岛景观所占的比重下降,优势度逐渐降低;多样性指数、均匀度指数总体呈上升趋势,各热岛景观面积在各类型间的分配逐渐趋于均匀;热岛景观斑块的转化方面,在20 a间低等级斑块类型(1、2、3级)向高等级斑块类型(4、5、6级)转化的面积总体上呈增加趋势,而高等级斑块类型向低等级斑块类型转化的面积总体上呈减小趋势,且等级升高的面积明显大于同期等级降低的面积;就高等级热岛景观斑块而言,他们与3级热岛景观斑块间的相互转化最容易发生,远比高等级斑块内部各类型之间的相互转化来得容易,尤其6类和5类的转化是最为困难的热岛景观变化之一;从空间上看,各高等级热岛景观斑块都经历了数量增加、面积扩大、等级升高三个方面的变化,形成了海沧、新阳、杏林、厦门岛西北港口区和机场5个高温组团。利用景观指数分析城市热环境,可探明热岛景观随城市化演变的趋势,并为有效的热岛效应减缓措施提供直接的理论依据。     

乳酸菌微机检索软件的开发

以现有乳酸菌信息为依据,利用汉字foxbase^＋2．10进行数据处理,研制出一套乳酸菌微机检索软件。该软件的特点：检索速度快,途径灵活,增添、修改、删除、打印方便,各模块性能优良,实用性强。     

荧光假单胞菌抗噬菌体菌株的选育

本实验从荧光假单胞菌（Ｐｓｅｕｄｏｍｏｎａｓｆｌｕｏｒｅｓｃｅｎｓ）ＡＳ—３菌株的不正常发酵液中分离到一种噬菌体,将其命名为ＰＦＡＳ。ＡＳ—３菌株能利用葡萄糖发酵产生Ｄ－异维生素Ｃ的前体物质２－酮基－Ｄ－葡萄糖酸。电镜观察表明ＰＦＡＳ噬菌体呈蝌蚪形,具有直径为６６ｎｍ的六角形头部及长１１７ｎｍ的尾部。通过紫外线诱变及自然选育两种途径,配合简便有效的初筛方法,经多次分离、纯化、复筛最终在摇并发酵试验中获得６株产量稳定地高于对照敏感菌的抗噬菌体菌株,可望用于生产。     

松嫩草原不同演替阶段大型土壤动物功能类群特征

大型土壤动物处于整个土壤食物网的最顶端,其各功能类群控制着其他动物所需资源的有效性,是土壤生态系统的重要组成部分。为了查明松嫩草原大型土壤动物的功能类群特征,在2006年5—10月期间,逐月对松嫩草原羊草、羊草+虎尾草、虎尾草、碱茅、碱蓬和光碱斑6个演替阶段大型土壤动物的功能类群组成、结构、多样性等特征进行研究。依据其食性将该区土壤动物划分为杂食性、植食性、捕食性和腐食性4个功能类群其中,杂食性土壤动物个体密度所占比例最多为39.16%,植食性土壤动物的类群数所占比例最多为50.00%,腐食性土壤动物个体密度和类群数所占比例均最小,分别为8.09%和12.82%。各功能类群土壤动物个体密度和类群数的相关性不显著(P0.05)。从水平结构来看,总体上各功能类群土壤动物在羊草群落和羊草+虎尾草群落个体密度和类群数较多,在无植被的光碱斑生境土壤动物的个体密度和类群数较少,植食性土壤动物的个体密度和类群数、杂食性土壤动物个体密度、腐食性土壤动物个体密度和类群数随着群落演替发生显著的变化(P0.01)。植食性和腐食性土壤动物个体密度和类群数相关性显著(P0.05)。垂直结构上,0—10 cm土层和20—30 cm土层除捕食性土壤动物个体密度以外,其它各功能类群土壤动物个体密度随着群落演替发生显著的变化(P0.05或P0.01);10—20 cm土层,除腐食性土壤动物个体密度以外,其它各功能类群土壤动物个体密度随着群落演替发生显著的变化(P0.05或P0.01)。0—10cm土层,植食性和杂食性土壤动物个体密度(P0.05)相关性显著;10—20 cm土层,植食性和腐食性土壤动物个体密度(P0.05)相关性显著。不同演替阶段对各功能类群土壤动物的多样性影响程度有所不同。4种功能类群土壤动物在羊草群落和光碱斑之间相似性指数较低,个体数量组成在演替初期的羊草群落和演替后期的光碱斑差异比较大。以上研究结果表明,松嫩草原不同退化演替阶段能够降低大型土壤动物功能类群组成和结构复杂性。