Summary

这在朱庇特11月

Published: November 01, 2011
doi:

Summary

Abstract

可视化实验杂志11月号开始的一系列行为实验测量捏在灵长类动物的能力。弗里堡大学的调查表明四个把握和深远的任务,都遵循共同的步骤舒适限制动物和正确定位其头部。布林克曼板测试是用来评估达到静态的对象,而旋转布林克曼委员会提出了一个条件,动物需要预见到对象的位置。布林克曼盒测试让灵巧的猴子有较少的自由程度执行抓任务,不能使用视觉引导运动的条件下进行调查。虽然布林克曼板和框测试,仅仅依靠在实验中获得的视频分析,以生成数据,达到任务仪器抽屉探测器监测的抓地力和负载部队以及抽屉的位置,使得本次测试appropriate测量强度以及捏能力。在这四个测试相结合,提供了一个强大的方法来评估电机控制远端前肢,弗里堡组从病变的研究和实验的目的是测试潜在的治疗脊髓损伤的数据。

在临床和转化医学,在苏黎世大学医院的外科研究部,并在苏黎世大学实验动物科学学院,携手合作,在小鼠体内植入一个无线电遥测装置,可用于生理测量的合作者自由移动的动物。该设备由两根导线,它能够测量生物电位活动(心电图,脑电图,肌电图),以及温度,和一个轻量级的无线电发射器(1-200赫兹的带宽),可在腹腔植入。动物处理压力以及麻醉已知的混杂因素,影响生理人测量,无线电遥测装置是一种方便的方式获取动物在生理数据泰然自若,自然状态,以及采取多种动物的测量,同时。

朱庇特也增加了其电击协议的主机与方法引入开发非洲爪蟾蝌蚪的颅面间质macromoledules在伦敦国王学院的刘的实验室,。爪蟾蝌蚪电击室,在那里他们可以与核酸注入,并受到电击,这将传递到发展中国家的颅面部组织的表达载体或morpholinos的转移。基因运送到差异化软骨本身的问题,刘实验室,通过elecroporation,morpholinos可成爪蟾蝌蚪procartilaginous和软骨组织的整个一系列的发展阶段。

在生物工程,朱克曼集团劳伦斯伯克利国家实验室的说明他们的方法,一类类似肽的生物活性有机分子合成peptoids,但其侧链的α碳,这使得它们耐水解肽键的氮,而不是, 。朱克曼集团演示submonomer合成肽单体加入顺序bromoacetylation和溴置换反应,允许精确控制peptoid链的长度和组成。此外,酰胺树脂,合成,并因此,固相合成,大大简化了纯化合成peptoids的。这些作者还表明,新合成的peptoids可诱导自组装成高度有序的结构,被称为纳米片,它可以通过荧光光谱和扫描电子显微镜观察。这些纳米片可以作为一个潜在的平台为蛋白质和膜MIMETICS。

在本月稍后,朱庇特的功能用于测量在我们的免疫和感染的临床抗体样品暴露细胞吞噬活性的检测。来自马萨诸塞州总医院和达特茅斯学院显示THP – 1细胞吞噬timelapse视频显微镜约束抗体抗原包被的磁珠,目前板的流量仪检测方法量化吞噬的程度的合作者。我们的作者使用此方法来确定不同的抗体样本能够诱导细胞的吞噬功能,如艾滋病患者的治疗和抗逆转录病毒疗法未处理的。

这朱庇特的在11月的内容摘要,提供了一个月的朱庇特的亮点简要概述。其他值得一提的文章,包括内皮细胞骨架的动态实时成像的方法,测量心肌细胞中的钙通量,片成人出生的嗅球中的神经元的电。

Protocol

Measuring Fast Calcium Fluxes in Cardiomyocytes Urszula Golebiewska1, Suzanne Scarlata21Department of Biological Sciences and Geology, Queensborough Community College, 2Department of Physiology & Biophysics, Stony Brook University We present a method to isolate rapid (microsecond) calcium events from slower fluxes in living cells using laser scanning confocal microscopy. The method measures fluorescence intensity fluctuations of calcium indicators by recording line scans of several hundred pixels in a cell. Histogram analysis allows us to isolate the time scales of different calcium fluxes. Solid-phase Submonomer Synthesis of Peptoid Polymers and their Self-Assembly into Highly-Ordered Nanosheets Helen Tran, Sarah L. Gael, Michael D. Connolly, Ronald N. ZuckermannMolecular Foundry, Lawrence Berkeley National Laboratory A simple and general manual peptoid synthesis method involving basic equipment and commercially available reagents is outlined, enabling peptoids to be easily synthesized in most laboratories. The synthesis, purification and characterization of an amphiphilic peptoid 36mer is described, as well as its self-assembly into highly-ordered nanosheets. Behavioral Assessment of Manual Dexterity in Non-Human Primates Eric Schmidlin*, Mélanie Kaeser*, Anne- Dominique Gindrat, Julie Savidan, Pauline Chatagny, Simon Badoud, Adjia Hamadjida, Marie-Laure Beaud, Thierry Wannier, Abderraouf Belhaj-Saif, Eric M. RouillerDepartment of Medicine, University of Fribourg* These authors contributed equally As manual dexterity is a prerogative mainly of primates, behavioral tasks have been developed in macaque monkeys. Four reach and grasp prehension tasks, measuring hand manipulation ability and force, allow to establish functional recovery after a lesion of the central nervous system and to test the effect of a treatment. Determining the Phagocytic Activity of Clinical Antibody Samples Elizabeth G. McAndrew1, Anne-Sophie Dugast1, Anna F. Licht1, Justin R. Eusebio1, Galit Alter1, Margaret E. Ackerman21Massachusetts General Hospital, Ragon Institute of MGH, MIT, and Harvard, 2Thayer School of Engineering, Dartmouth College We present a high-throughput flow cytometric assay to determine the phagocytic activity of antigen-specific antibodies from clinical samples, utilizing fluorescent antigen-coated beads and a monocytic cell line expressing multiple Fc receptors-providing receptor usage and phagocytic activity determinations in a standardized and reproducible fashion for any antigen of interest. Study of the Actin Cytoskeleton in Live Endothelial Cells Expressing GFP-Actin Travis M. Doggett, Jerome W. BreslinDepartment of Physiology, Louisiana State University Health Sciences Center Microscopic imaging of live endothelial cells expressing GFP-actin allows characterization of dynamic changes in cytoskeletal structures. Unlike techniques that use fixed specimens, this method provides a detailed assessment of temporal changes in the actin cytoskeleton in the same cells before, during, and after various physical, pharmacological, or inflammatory stimuli. Implantation of Radiotelemetry Transmitters Yielding Data on ECG, Heart Rate, Core Body Temperature and Activity in Free-Moving Laboratory Mice Nikola Cesarovic1, Paulin Jirkof2, Andreas Rettich2, Margarete Arras11Division of Surgical Research, University Hospital Zurich, 2Institute of Laboratory Animal Science, University of Zurich A surgical technique for implantation of commercially available telemetry transmitters used for continuous measurement of biopotential (one-lead ECG), heart rate, core body temperature and locomotor activity in freely moving mice is shown. Recommendations and protocols for post-operative care and pain relief, improving recovery, wellbeing and survival rate are also presented. Electroporation of Craniofacial Mesenchyme Jacqueline M. Tabler, Karen J. LiuDepartment of Craniofacial Development, King's College London Craniofacial cartilages develop in close contact with other tissues and are difficult to manipulate in live animals. We are using electroporation to deliver molecular tools during growth of the craniofacial skeleton while bypassing early embryonic effects. This approach will allow us to efficiently test candidate molecules in vivo. Slice Electrophysiological Recording and Optogenetic Stimulation of Adult-Born Neurons in the Olfactory Bulb Matthew Valley, Sebastian Wagner, Benjamin W. Gallarda, Pierre-Marie LledoLaboratory for Perception and Memory, Institut Pasteur and Centre National de la Recherche Scientifique (CNRS) Adult-born neurons expressing ChR2 can be manipulated in slice electrophysiological preparations in order to examine their contribution towards the function of olfactory neural circuits.

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Kolski-Andreaco, A. November 2011: This Month in JoVE. J. Vis. Exp. (57), e4025, doi:10.3791/4025 (2011).

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