Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2005-6-28
pubmed:abstractText
P2X7 is a bifunctional receptor (P2X7R) for extracellular ATP that, depending on the level of activation, forms a cation-selective channel or a large conductance nonselective pore. The P2X7R has a strong proapoptotic activity but can also support growth. Here, we describe the mechanism involved in growth stimulation. Transfection of P2X7R increases resting mitochondrial potential (delta psi(mt)), basal mitochondrial Ca2+ ([Ca2+]mt), intracellular ATP content, and confers ability to grow in the absence of serum. These changes require a full pore-forming function, because they are abolished in cells transfected with a mutated P2X7R that retains channel activity but cannot form the nonselective pore, and depend on an autocrine/paracrine tonic stimulation by secreted ATP. On the other hand, sustained stimulation of P2X7R causes a delta psi(mt) drop, a large increase in [Ca2+]mt, mitochondrial fragmentation, and cell death. These findings reveal a hitherto undescribed mechanism for growth stimulation by a plasma membrane pore.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-10559192, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-10570154, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-10802706, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-11080249, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-11157473, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-11166569, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-11707406, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-11728343, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-11781259, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-11884276, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-12080052, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-12270951, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-12624920, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-12684505, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-12857854, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-12869560, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-12880424, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-14559818, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-14987223, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-15331685, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-15383600, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-7495489, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-7552174, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-7883969, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-8063855, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-8235595, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-8614837, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-9038151, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-9714601, http://linkedlifedata.com/resource/pubmed/commentcorrection/15901833-9876159
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1059-1524
pubmed:author
pubmed:issnType
Print
pubmed:volume
16
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3260-72
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:15901833-Adenosine Triphosphate, pubmed-meshheading:15901833-Animals, pubmed-meshheading:15901833-Calcium, pubmed-meshheading:15901833-Cell Line, pubmed-meshheading:15901833-Cell Membrane, pubmed-meshheading:15901833-Cell Proliferation, pubmed-meshheading:15901833-Culture Media, Serum-Free, pubmed-meshheading:15901833-Cytosol, pubmed-meshheading:15901833-Gene Deletion, pubmed-meshheading:15901833-HeLa Cells, pubmed-meshheading:15901833-Humans, pubmed-meshheading:15901833-Ions, pubmed-meshheading:15901833-Membrane Potentials, pubmed-meshheading:15901833-Mitochondria, pubmed-meshheading:15901833-Models, Molecular, pubmed-meshheading:15901833-Receptors, Purinergic P2, pubmed-meshheading:15901833-Receptors, Purinergic P2X7, pubmed-meshheading:15901833-Time Factors, pubmed-meshheading:15901833-Transfection
pubmed:year
2005
pubmed:articleTitle
Basal activation of the P2X7 ATP receptor elevates mitochondrial calcium and potential, increases cellular ATP levels, and promotes serum-independent growth.
pubmed:affiliation
Department of Experimental and Diagnostic Medicine, Section of General Pathology, and Interdisciplinary Center for the Study of Inflammation, University of Ferrara, 44100 Ferrara, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't