Source:http://linkedlifedata.com/resource/pubmed/id/15016615
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2004-6-14
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pubmed:abstractText |
Upregulation of CGRP-immunoreactive (IR) primary afferent nerve fibers accompanied by mastocytosis is characteristic for the Schistosoma mansoni-infected murine ileum. These mucosal mast cells (MMC) and CGRP-IR fibers, which originate from dorsal root (DRG) and nodose ganglia, are found in close apposition. We examined interactions between primary cultured MMC and CGRP-IR DRG neurons in vitro by confocal recording of intracellular Ca(2+) concentration ([Ca(2+)](i)). The degranulatory EC(50) for the mast cell secretagogue compound 48/80 (C48/80; 10 microg/ml) and the neuropeptides CGRP (2.10(-8) M) and substance P (SP; 3.10(-8) M) were determined by measurement of extracellular release of the granule chymase, mouse mast cell protease-1. Application of C48/80 (10 microg/ml) and CGRP and SP (both 10(-7) M) to Fluo-4-loaded MMC induced a transient rise in [Ca(2+)](i) after a lag time, indicative of mast cell degranulation and/or secretion. The CGRP response could be completely blocked by pertussis toxin (2 microg/ml), indicating involvement of G(i) proteins. Application of MMC juice, obtained by C48/80 degranulation of MMC, to Fluo-4-loaded DRG neurons induced in all neurons a rise in [Ca(2+)](i), indicative of activation. Degranulation of MMC by C48/80 in culture dishes containing Fluo-4-loaded DRG neurons also caused activation of the DRG neurons. In conclusion, these results demonstrate a bidirectional cross-talk between cultured MMC and CGRP-IR DRG neurons in vitro. This indicates that such a communication may be the functional relevance for the close apposition between MMC and CGRP-IR nerve fibers in vivo.
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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 |
Jul
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pubmed:issn |
0193-1857
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
287
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
G178-91
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15016615-Animals,
pubmed-meshheading:15016615-Body Fluids,
pubmed-meshheading:15016615-Calcitonin Gene-Related Peptide,
pubmed-meshheading:15016615-Calcium,
pubmed-meshheading:15016615-Cell Degranulation,
pubmed-meshheading:15016615-Cells, Cultured,
pubmed-meshheading:15016615-Ganglia, Spinal,
pubmed-meshheading:15016615-Intestinal Mucosa,
pubmed-meshheading:15016615-Intracellular Membranes,
pubmed-meshheading:15016615-Male,
pubmed-meshheading:15016615-Mast Cells,
pubmed-meshheading:15016615-Mice,
pubmed-meshheading:15016615-Neurons,
pubmed-meshheading:15016615-Osmolar Concentration,
pubmed-meshheading:15016615-Substance P,
pubmed-meshheading:15016615-p-Methoxy-N-methylphenethylamine
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pubmed:year |
2004
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pubmed:articleTitle |
In vitro activation of murine DRG neurons by CGRP-mediated mucosal mast cell degranulation.
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pubmed:affiliation |
Laboratory of Cell Biology and Histology, Department of Biomedical Sciences, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerp, Belgium. jean-pierre.timmermans@ua.ac.be
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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