Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
2006-6-8
pubmed:abstractText
We have developed a simple and sensitive assay to quantify neuron-specific death in primary cell cultures that represents a significant improvement over more commonly used methods including manual cell counting and lactate dehydrogenase release. This new method selectively detects neuronal death by combining immunolabeling for a neuron-specific marker with the ease, sensitivity, and speed of an enzyme-linked fluorescence assay. Using microtubule associated protein 2 (MAP2) as a neuron-specific marker, we assessed glutamate-receptor mediated neurotoxicity in neuron-enriched cultures and in mixed neuronal/glial cultures established from mouse forebrain and compared these results to neuronal death measured by lactate dehydrogenase (LDH) release. We were able to achieve statistically significant differences in toxicity between intermediately toxic concentrations of glutamate (30, 50, and 100 microM) with the MAP2 assay, while we were not able to discriminate among these concentrations with the LDH assay. We were also able to measure hydrogen peroxide-induced neuronal death, and demonstrate neuroprotection by antioxidant addition. This new assay is easily adaptable to high-throughput in vitro screens of neurodegeneration and of neuroprotective therapies.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0165-0270
pubmed:author
pubmed:issnType
Print
pubmed:day
30
pubmed:volume
154
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
239-44
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:16483667-Animals, pubmed-meshheading:16483667-Antioxidants, pubmed-meshheading:16483667-Biological Assay, pubmed-meshheading:16483667-Cell Death, pubmed-meshheading:16483667-Cell Survival, pubmed-meshheading:16483667-Cells, Cultured, pubmed-meshheading:16483667-Coculture Techniques, pubmed-meshheading:16483667-Excitatory Amino Acids, pubmed-meshheading:16483667-Fluorescent Antibody Technique, pubmed-meshheading:16483667-Glial Fibrillary Acidic Protein, pubmed-meshheading:16483667-Glutamic Acid, pubmed-meshheading:16483667-Hydrogen Peroxide, pubmed-meshheading:16483667-L-Lactate Dehydrogenase, pubmed-meshheading:16483667-Male, pubmed-meshheading:16483667-Mice, pubmed-meshheading:16483667-Microtubule-Associated Proteins, pubmed-meshheading:16483667-Nerve Degeneration, pubmed-meshheading:16483667-Neuroglia, pubmed-meshheading:16483667-Neuroprotective Agents, pubmed-meshheading:16483667-Oxazines, pubmed-meshheading:16483667-Oxidants
pubmed:year
2006
pubmed:articleTitle
A sensitive and selective assay of neuronal degeneration in cell culture.
pubmed:affiliation
Division of Pharmacology, The Ohio State University, Columbus, 43210, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural