Name: January 2012: This Month in JoVE (Video) | JoVE Journal
Uploaded: 2012-01-02T00:00:00.000+00:00
Duration: 5 min 9 s
Description: Discover innovative neuroscience and biology research from JoVE's January 2012 issue. Learn how visualized experimental protocols enhance reproducibility and understanding of complex biological processes.

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5 minutes

<h2 class="jove_title"><a href="https://www.jove.com/video/3122">Selection of Plasmodium falciparum Parasites for Cytoadhesion to Human Brain Endothelial Cells</a></h2>
Antoine Claessens, J. Alexandra Rowe Centre for Immunity, Infection and Evolution, University of Edinburgh
An in vitro model for cerebral malaria sequestration is described1. Plasmodium falciparum infected red blood cells are selected for binding to immortalized human brain microvascular endothelial cells. The selected parasites show a distinct phenotype. The selection process can be applied using various P. falciparum strains and endothelial cell lines.
<h2 class="jove_title"><a href="https://www.jove.com/video/3308">Implantation of a Carotid Cuff for Triggering Shear-stress Induced Atherosclerosis in Mice</a></h2>
Michael T. Kuhlmann1, Simon Cuhlmann2, 3, Irmgard Hoppe1, Rob Krams3, Paul C. Evans2, Gustav J. Strijkers4, Klaas Nicolay4, Sven Hermann1, Michael Sch&#228;fers1 1European Institute for Molecular Imaging, Westf&#228;lische Wilhelms-University M&#252;nster, 2British Heart Foundation Cardiovascular Sciences Unit, Imperial College London , 3Department of Bioengineering, Imperial College London , 4Biomedical Engineering, Eindhoven University of Technology
The constricting cuff presented in this article is designed to induce atherosclerosis in the murine common carotid artery. Due to the conical shape of its inner lumen the implanted cuff generates well-defined regions of low, high and oscillatory shear stress triggering the development of atherosclerotic lesions of different inflammatory phenotypes.
<h2 class="jove_title"><a href="https://www.jove.com/video/3330">Analysis of Trunk Neural Crest Cell Migration using a Modified Zigmond Chamber Assay</a></h2>
Christopher C. Walheim1, Juan Pablo Zanin2, Maria Elena de Bellard1 1Department of Biology, California State University, Northridge, 2Centro de Biolog&#237;a Celular y Molecular, Universidad Nacional de C&#243;rdoba
An approach to analyze the migration of explanted cells (trunk neural crest cells) is described. This method is inexpensive, gentle, and capable of distinguishing chemotaxis from both chemokinesis and other influences on migratory polarity such as those derived from cell-cell interactions within the primary trunk neural crest cell culture.
<h2 class="jove_title"><a href="https://www.jove.com/video/3350">Organotypic Slice Cultures of Embryonic Ventral Midbrain: A System to Study Dopaminergic Neuronal Development in vitro</a></h2>
Gabriela Oana Bodea, Sandra Blaess Institute of Reconstructive Neurobiology, University of Bonn
A method to generate organotypic slices from the E12.5 murine embryonic midbrain is described. The organotypic slice cultures can be used to observe the behavior of dopaminergic neurons or other ventral midbrain neurons.
<h2 class="jove_title"><a href="https://www.jove.com/video/3362">Visualization of Caenorhabditis elegans Cuticle Structures using the Lipophilic Vital Dye, DiI</a></h2>
Robbie D. Schultz1, 2, Tina L. Gumienny2 1Department of Molecular and Cellular Medicine, Texas A&#38;M University System Health Science Center, 2Department of Molecular and Cellular Medicine, Texas A&#38;M University System Health Science Center, College of Medicine
We present a method to visualize cuticle in live C. elegans using the red fluorescent lipophilic dye DiI (1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate), which is commonly used in C. elegans to visualize environmentally exposed neurons. With this optimized protocol, alae and annular cuticular structures are stained by DiI and observed using compound microscopy.
<h2 class="jove_title"><a href="https://www.jove.com/video/3406">A Protocol for Detecting and Scavenging Gas-phase Free Radicals in Mainstream Cigarette Smoke</a></h2>
Long-Xi Yu1, Boris G. Dzikovski2, Jack H. Freed3, 2 1CDCF-AOX Lab, 2National Biomedical Center for Advanced ESR Technology (ACERT), Department of Chemistry and Chemical Biology, Cornell University, 3ACERT Research, Center Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University
Spin-trapping ESR spectroscopy was used to study the effect of plant antioxidants lycopene, pycnogenol and grape seed extract on scavenging gas-phase free radicals in cigarette smoke.
<h2 class="jove_title"><a href="https://www.jove.com/video/3417">How to Measure Cortical Folding from MR Images: A Step-by-step Tutorial to Compute Local Gyrification Index</a></h2>
Marie Schaer1, Meritxell Bach Cuadra2, 3, Nick Schmansky4, Bruce Fischl4, Jean-Philippe Thiran2, Stephan Eliez1 1Department of Psychiatry, University of Geneva School of Medicine, 2Signal Processing Laboratory, &#201;cole Polytechnique F&#233;d&#233;rale de Lausanne, 3Department of Radiology, University Hospital Center and University of Lausanne, 4Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital
Measuring gyrification (cortical folding) at any age represents a window into early brain development. Hence, we previously developed an algorithm to measure local gyrification at thousands of points over the hemisphere1. In this paper, we detail the computation of this local gyrification index.
<h2 class="jove_title"><a href="https://www.jove.com/video/3551">The Use of Thermal Infra-Red Imaging to Detect Delayed Onset Muscle Soreness</a></h2>
Hani H. Al-Nakhli1, Jerrold S. Petrofsky1, 2, Michael S. Laymon2, Lee S. Berk1 1Loma Linda University, 2Azusa Pacific University
The purpose of this investigation was to assess whether using an infra-red thermal camera is a valid tool for detecting and quantifying the muscle soreness after exercising.

january 2012: this month in jove

January 2012: This Month in JoVE

The Journal of Visualized Experiments (JoVE) begins 2012 by publishing its 1500th article, which focuses on a method for analyzing the free radical composition of cigarette smoke. Although tobacco tar is thought to be the most carcinogenic agent in cigarette smoke, free radicals are well known cancer-causing molecules, and the level of these carcinogens contained in cigarette smoke is not currently known. The method employed in this article combines the use of a single-port smoking device, which simulates cigarette puffing, with electron spin resonance (ESR) spectroscopy, a technique, which measures the spin energy emitted by the unpaired electrons in free radicals. One important modification of the single port smoking device used in this article, is the introduction of a liquid nitrogen trap in front of the spin trap. Liquid nitrogen removes water vapor from cigarette smoke and greatly improves ESR spectra as a result.
In addition to measuring the free radical concentration found in cigarette smoke, plant antioxidants are introduced into modified cigarette filters and the ESR spectra of cigarette smoke passed through these filters is obtained. Grape seed extract and lycopene were observed to have the most significant scavenging effects on free radicals, and if cost effective means of including these molecules into cigarette filters can be developed, a less harmful cigarette could be created.
In Clinical and Translational Medicine, JoVE presents an analytical method for determining the local Gyrification Index (lGI) - a measurement of the extent of cortical folding. Cortical folds develop during the first few post natal months, and adverse events during this time can lead to abnormalities in the brain's surface anatomy, which may ultimately correlate with neuropsychiatric disorders.
The analysis tool developed for calculating the local Gyrification Index is Freesurfer, which can convert T1 weighted MRI scans into 3D reconstructions of the cortex. Separate reconstructions are created for the grey/white mater and grey/pial interfaces, which are manually adjusted before computating the lGI. Following a smoothing operation, circular regions of the pial and grey/white surfaces are compared, in order to compute the lGI for thousands of points over the entire brain. Freesurfer makes analysis of gyrification straightforward and accessible to clinicians and brain scientists, who are interested in comparing the extent of cortical folding between different individuals in normal and disease states.
JoVE's Immunology and Infection article for the month of January continues the journal's tradition of publishing cutting edge methodology in vector born disease research. Specifically, this article adds to JoVE's comprehensive collection of protocols for malaria research by extending our library to cerebral malaria - a devastating condition with high susceptibility in children. Briefly, this protocol involves exposing a monolayer of human brain endothelial cells, passaged onto petri dishes, to Plasmodium falciparum-infected red blood cells. Following washing and enriching steps, high yields of parasites, which carry the potential to infect the brain, can be isolated and further characterized.
In Neuroscience, JoVE showcases a method for studying the migration of neural crest cells. These cells are a transient, multipotent, developmental cell type that can, in addition to becoming neuronal tissue, differentiate into smooth muscle, chromaffin cells, cartiliage, and bone. Chick embryos are carefully prepared, so that the trunk region can be isolated and the neural tube excised for overnight culture on fibronectin-coated coverslips, which allows neural crest cells to emigrate from the neural tube. Following removal of the neural tube, coverslips containing the cultured neural crest cells are transferred to a modified Zigmond chamber - a chamber which enables a concentration gradient of putative chemotactic agent to be established across the culture. Timelapes imaging followed by analysis of cell trajectories, is used to assess the chemotactic potential of molecules loaded into the zigmund chamber, providing insight into the molecular cues that guide migration of this important developmental cell type.
These featured articles comprise four of fifty video-protocols for release in January. Other notable articles include methods for visualizing the cuticle structures of c. elegans, thermal imaging of delayed onset muscle soreness, culturing the ventral midbrain in organotypic slices, and inducing atherosclerosis in mice.

Here are some highlights from the January 2012 Issue of Journal of Visualized Experiments (JoVE).

The Journal of Visualized Experiments (JoVE) begins 2012 by publishing its 1500th article, which focuses on a method for analyzing the free radical ...

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Discover innovative neuroscience and biology research from JoVE's January 2012 issue. Learn how visualized experimental protocols enhance reproducibility and understanding of complex biological processes.

January 2012: This Month in JoVE (Video) | JoVE Journal

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January 2012: This Month in JoVE

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