Source:http://linkedlifedata.com/resource/pubmed/id/21162127
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2010-12-16
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pubmed:abstractText |
Chemokines can be produced by gliomas, which mediate the infiltration of microglia, a characteristic feature of glioma-associated neuropathogenesis. ATP that is released at a high level from glioma has been reported to play a regulatory role in chemokine production in cultured glioma cells. The objective of this study was to define the potential role of extracellular ATP in the regulation of macrophage inflammatory protein-1? (MIP-1?) and monocyte chemoattractant protein-1(MCP-1) expression in glioma-associated microglia/macrophages. The results showed that Iba1(+) and ED1(+) microglia existed in the tumor at 3 and 7 day after injection of C6 glioma cells into the rat cerebral cortex (dpi). ED1(+) microglia/macrophages or Iba1(+) microglia in the glioma were also colocalized to MIP-1?- and MCP-1-expressing cells. In vitro study indicated that treatment with ATP and BzATP (an agonist for ATP ionotropic receptor P2X?R) caused an increase in the intracellular levels of microglial MIP-1? and MCP-1. By using an extracellular Ca(2+) chelator (EGTA) and P2X?R antagonists, oxidized ATP (oxATP) and brilliant blue G (BBG), we demonstrated that BzATP-induced production of MIP-1? and MCP-1 levels was due to P2X?R activation and Ca(2+) -dependent regulation. Coadministration of C6 glioma cells and oxATP into the rat cerebral cortex resulted in a reduction of MIP-1?- and MCP-1-expressing microglia/macrophages. We suggest, based on the results from in vivo and in vitro studies, that a massive amount of ATP molecules released in the glioma tumor site may act as the regulator with P2X?R signaling that increases MIP-1? and MCP-1 expression in tumor-infiltrating microglia/macrophages.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Ccl2 protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL2,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL3,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Purinergic P2X
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1097-4547
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Wiley-Liss, Inc.
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pubmed:issnType |
Electronic
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pubmed:volume |
89
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
199-211
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pubmed:meshHeading |
pubmed-meshheading:21162127-Adenosine Triphosphate,
pubmed-meshheading:21162127-Animals,
pubmed-meshheading:21162127-Cell Line, Tumor,
pubmed-meshheading:21162127-Chemokine CCL2,
pubmed-meshheading:21162127-Chemokine CCL3,
pubmed-meshheading:21162127-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:21162127-Female,
pubmed-meshheading:21162127-Fluorescent Antibody Technique,
pubmed-meshheading:21162127-Gene Expression,
pubmed-meshheading:21162127-Gene Expression Regulation,
pubmed-meshheading:21162127-Glioma,
pubmed-meshheading:21162127-Immunohistochemistry,
pubmed-meshheading:21162127-Microglia,
pubmed-meshheading:21162127-Rats,
pubmed-meshheading:21162127-Rats, Sprague-Dawley,
pubmed-meshheading:21162127-Receptors, Purinergic P2X
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pubmed:year |
2011
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pubmed:articleTitle |
Expression of macrophage inflammatory protein-1? and monocyte chemoattractant protein-1 in glioma-infiltrating microglia: involvement of ATP and P2X? receptor.
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pubmed:affiliation |
Department of Life Sciences, National Cheng Kung University, Tainan, Taiwan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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