pubmed-article:1445262 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:1445262 | lifeskim:mentions | umls-concept:C0034721 | lld:lifeskim |
pubmed-article:1445262 | lifeskim:mentions | umls-concept:C0034693 | lld:lifeskim |
pubmed-article:1445262 | lifeskim:mentions | umls-concept:C0024880 | lld:lifeskim |
pubmed-article:1445262 | lifeskim:mentions | umls-concept:C0018328 | lld:lifeskim |
pubmed-article:1445262 | lifeskim:mentions | umls-concept:C0443286 | lld:lifeskim |
pubmed-article:1445262 | lifeskim:mentions | umls-concept:C0596235 | lld:lifeskim |
pubmed-article:1445262 | lifeskim:mentions | umls-concept:C1709060 | lld:lifeskim |
pubmed-article:1445262 | lifeskim:mentions | umls-concept:C0205224 | lld:lifeskim |
pubmed-article:1445262 | pubmed:dateCreated | 1992-12-22 | lld:pubmed |
pubmed-article:1445262 | pubmed:abstractText | Exocytosis from metabolically depleted permeabilized rat mast cells was measured in response to provision of Ca2+ and guanine nucleotide [GTP or guanosine 5'-[gamma-thio]triphosphate (GTP[S])]. For cells permeabilized in simple salt solutions (NaCl), both of these effectors were required to induce secretion. Exclusion of Mg2+ caused an increase in both the sensitivity of the system to GTP and the extent of secretion elicited, while having no such effects on secretion induced by GTP[S]. The effect of Mg2+ depletion on the ability of GTP to stimulate secretion is probably due to the dependence on Mg2+ of the GTPase activity of GE (a postulated GTP-binding protein which mediates exocytosis). This argues that a persistent stimulus to the G-protein is required to support secretion. Affinity for both GTP[S] and GTP is enhanced when the cells are permeabilized in zwitterionic electrolytes (glutamate, gamma-aminobutyric acid, glycine) instead of NaCl. Under these conditions, secretion occurs in response to provision of either GTP[S] [in the effective absence of Ca2+ (pCa 9)] or Ca2+ (in the absence of guanine nucleotide). Secretion induced by GTP[S] is strongly promoted by the presence of Mg2+ at concentrations in the millimolar range; this promotion by Mg2+ declines as the concentration of Ca2+ is elevated towards pCa 7. At pCa 6, Mg2+ is without effect. Ca(2+)-induced secretion requires the provision of MgATP. Since this is further enhanced by low concentrations (< 100 microM) and then inhibited by high concentrations of GDP, the essential role of ATP is likely to be in the maintenance of GTP via transphosphorylation by a nucleoside diphosphate kinase reaction. Thus, under conditions of high affinity (glutamate environment), GTP[S] alone is capable of inducing exocytosis. Ca2+ acts in concert with guanine nucleotides: it enhances the rate and extent of secretion and increases the affinity for Mg2+ and guanine nucleotides in the activation of the GTP-binding protein (GE) which regulates exocytosis. | lld:pubmed |
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pubmed-article:1445262 | pubmed:language | eng | lld:pubmed |
pubmed-article:1445262 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1445262 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:1445262 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:1445262 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:1445262 | pubmed:month | Nov | lld:pubmed |
pubmed-article:1445262 | pubmed:issn | 0264-6021 | lld:pubmed |
pubmed-article:1445262 | pubmed:author | pubmed-author:GompertsB DBD | lld:pubmed |
pubmed-article:1445262 | pubmed:author | pubmed-author:LillieT HTH | lld:pubmed |
pubmed-article:1445262 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:1445262 | pubmed:day | 15 | lld:pubmed |
pubmed-article:1445262 | pubmed:volume | 288 ( Pt 1) | lld:pubmed |
pubmed-article:1445262 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:1445262 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:1445262 | pubmed:pagination | 181-7 | lld:pubmed |
pubmed-article:1445262 | pubmed:dateRevised | 2010-9-7 | lld:pubmed |
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pubmed-article:1445262 | pubmed:year | 1992 | lld:pubmed |
pubmed-article:1445262 | pubmed:articleTitle | Guanine nucleotide is essential and Ca2+ is a modulator in the exocytotic reaction of permeabilized rat mast cells. | lld:pubmed |
pubmed-article:1445262 | pubmed:affiliation | Department of Physiology, University College London, U.K. | lld:pubmed |
pubmed-article:1445262 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:1445262 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |