Source:http://linkedlifedata.com/resource/pubmed/id/15662620
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2005-1-26
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pubmed:abstractText |
Sensory mechanisms in teeth are not well understood and may involve pulpal-neural interactions. Tooth cells that proliferate in vitro have polyclonal immunoreactivity (IR) for glial fibrillary acidic protein (GFAP), growth-associated protein (GAP-43), and vimentin, plus glial-like ion channels. Here, we analyzed GFAP-IR patterns in dental and trigeminal tissues of rats, for comparison with green fluorescent protein (GFP) associated with GFAP transcription in transgenic mice, in order to better characterize glial-like cells in dental tissues. Astrocytes, ganglion satellite cells, and epineurial Schwann cells were demonstrated by anti-GFAP antibodies and GFP-GFAP, as expected. Odontoblasts did not stain by any of these methods and cannot be the glial-like cells. Fibroblasts and undifferentiated mesenchymal cells in pulp had polyclonal GFAP-IR and vimentin-IR, while nerve fibers reacted only with polyclonal antibody. Some Schwann cell subtypes in trigeminal nerve and oral mucosa were positive for GFP and for polyclonal anti-GFAP, but not for monoclonal antibody. In pulp almost all Schwann cells were unstained, but many Schwann cells in periodontal ligament had polyclonal GFAP-IR. These results show greater heterogeneity for Schwann cells than expected, and suggest that the glial-like pulp cells are fibroblasts and/or undifferentiated mesenchymal cells or stem cells. We also found that polyclonal GFAP revealed intermediate filaments in preterminal sensory nerve fibers, thereby providing a useful marker for that neural subregion. GFP transcription by some Schwann cell subtypes in oral mucosae and trigeminal nerve, but not trigeminal root was a novel finding that reveals more complexity in peripheral glia than previously recognized.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1059-910X
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2005 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:volume |
65
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
295-307
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:15662620-Animals,
pubmed-meshheading:15662620-Dental Pulp,
pubmed-meshheading:15662620-Female,
pubmed-meshheading:15662620-Gingiva,
pubmed-meshheading:15662620-Glial Fibrillary Acidic Protein,
pubmed-meshheading:15662620-Immunohistochemistry,
pubmed-meshheading:15662620-Male,
pubmed-meshheading:15662620-Mice,
pubmed-meshheading:15662620-Mice, Transgenic,
pubmed-meshheading:15662620-Mouth Mucosa,
pubmed-meshheading:15662620-Odontoblasts,
pubmed-meshheading:15662620-Periodontal Ligament,
pubmed-meshheading:15662620-Rats,
pubmed-meshheading:15662620-Rats, Sprague-Dawley,
pubmed-meshheading:15662620-Transcription, Genetic,
pubmed-meshheading:15662620-Trigeminal Ganglion,
pubmed-meshheading:15662620-Vimentin
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pubmed:year |
2004
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pubmed:articleTitle |
GFAP immunoreactivity and transcription in trigeminal and dental tissues of rats and transgenic GFP/GFAP mice.
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pubmed:affiliation |
Anesthesiology, University of Washington, Seattle, Washington 98195, USA. byersm@u.washington.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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