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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1996-3-27
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pubmed:abstractText |
Molecular recognition processes between cell surface elements are discussed with special reference to cell surface pattern formation of membrane-bound integral proteins. The existence, as detected by flow cytometric resonance energy transfer (Appendix), and significance of cell surface patterns involving the interleukin-2 receptor, the T-cell receptor-CD3 system, the intercellular adhesion molecule ICAM-1, and the major histocompatibility complex class I and class II molecules in the plasma membrane of lymphocytes are described. The modulation of antigen presentation by transmembrane potential changes is discussed, and a general role of transmembrane potential changes, and therefore of ion channel activities, adduced as one of the major regulatory mechanisms of cell-cell communication. A general role in the mediation and regulation of intercellular interactions is suggested for cell-surface macromolecular patterns. The dynamic pattern of protein and lipid molecules in the plasma membrane is generated by the genetic code, but has a remarkable flexibility and may be one of the major instruments of accommodation and recognition processes at the cellular level.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD3,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Surface,
http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Adhesion Molecule-1,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-2
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pubmed:status |
MEDLINE
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pubmed:issn |
0952-3499
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
N
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pubmed:pagination |
237-46
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8588941-Animals,
pubmed-meshheading:8588941-Antigens, CD3,
pubmed-meshheading:8588941-Antigens, Surface,
pubmed-meshheading:8588941-Cell Communication,
pubmed-meshheading:8588941-Energy Transfer,
pubmed-meshheading:8588941-Flow Cytometry,
pubmed-meshheading:8588941-Humans,
pubmed-meshheading:8588941-Intercellular Adhesion Molecule-1,
pubmed-meshheading:8588941-Major Histocompatibility Complex,
pubmed-meshheading:8588941-Membrane Potentials,
pubmed-meshheading:8588941-Membrane Proteins,
pubmed-meshheading:8588941-Receptors, Antigen, T-Cell,
pubmed-meshheading:8588941-Receptors, Cell Surface,
pubmed-meshheading:8588941-Receptors, Interleukin-2
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pubmed:articleTitle |
Plasma-membrane-bound macromolecules are dynamically aggregated to form non-random codistribution patterns of selected functional elements. Do pattern recognition processes govern antigen presentation and intercellular interactions?
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pubmed:affiliation |
Department of Biophysics, University Medical School of Debrecen, Hungary.
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pubmed:publicationType |
Journal Article,
Review,
Research Support, Non-U.S. Gov't
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