Source:http://linkedlifedata.com/resource/pubmed/id/20394468
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2010-11-29
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pubmed:abstractText |
Adult mesenchymal stem cells (MeSCs) isolated from human bone marrow are capable of generating neural stem cell (NSC)-like cells that can be subsequently differentiated into cells expressing molecular markers for neurons. Here we report that these neuron-like cells had functional properties similar to those of brain-derived neurons. Whole-cell patch-clamp recordings and calcium imaging experiments were performed on neuron-like cells differentiated from bone-marrow-derived NSC-like cells. The neuron-like cells were subjected to current pulses to determine if they were capable of generating depolarization-induced action potentials. We found that nearly all of the cells with neuron-like morphology exhibited active membrane properties in response to the depolarizing pulses. The most common response was a single spike-like event with an overshoot and brief afterhyperpolarization. Cells that did not generate overshooting spike-like events usually displayed rectifying current-voltage relationships. The prevalence of these active membrane properties in response to the depolarizing current pulses suggested that the human MeSCs (hMeSCs) were capable of converting to a neural lineage under defined culture conditions. The spike-like events were blocked by the voltage-gated sodium channel inhibitor lidocaine, but unaffected by another sodium channel inhibitor tetrodotoxin (TTX). In calcium imaging experiments, the neuron-like cells responded to potassium chloride depolarization and l-glutamate application with increases in the cytoplasmic calcium levels. Thus, the neuron-like cells appeared to express TTX-resistant voltage-gated sodium channels, voltage-gated calcium channels, and functional l-glutamate receptors. These results demonstrate that hMeSCs were capable of generating cells with characteristics typical of functional neurons that may prove useful for neuroreplacement therapies.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Lidocaine,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels, Voltage-Gated,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Chloride,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Glutamate,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Tetrodotoxin
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1557-8534
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1831-41
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pubmed:dateRevised |
2011-8-31
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pubmed:meshHeading |
pubmed-meshheading:20394468-Action Potentials,
pubmed-meshheading:20394468-Biological Markers,
pubmed-meshheading:20394468-Bone Marrow Cells,
pubmed-meshheading:20394468-Calcium,
pubmed-meshheading:20394468-Calcium Channels,
pubmed-meshheading:20394468-Humans,
pubmed-meshheading:20394468-Lidocaine,
pubmed-meshheading:20394468-Membranes,
pubmed-meshheading:20394468-Mesenchymal Stem Cells,
pubmed-meshheading:20394468-Neural Stem Cells,
pubmed-meshheading:20394468-Neurons,
pubmed-meshheading:20394468-Patch-Clamp Techniques,
pubmed-meshheading:20394468-Potassium Channels, Voltage-Gated,
pubmed-meshheading:20394468-Potassium Chloride,
pubmed-meshheading:20394468-Receptors, Glutamate,
pubmed-meshheading:20394468-Sodium Channels,
pubmed-meshheading:20394468-Tetrodotoxin
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pubmed:year |
2010
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pubmed:articleTitle |
Membrane properties of neuron-like cells generated from adult human bone-marrow-derived mesenchymal stem cells.
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pubmed:affiliation |
Department of Pain Management, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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