pubmed-article:3782301 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C0006675 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C0010453 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C0332307 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C0001924 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C0014257 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C1383501 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C0597357 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C1622186 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C0019588 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C0033414 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C0442805 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C0392756 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C0012222 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C0872351 | lld:lifeskim |
pubmed-article:3782301 | lifeskim:mentions | umls-concept:C2827063 | lld:lifeskim |
pubmed-article:3782301 | pubmed:issue | 6 Pt 1 | lld:pubmed |
pubmed-article:3782301 | pubmed:dateCreated | 1987-1-15 | lld:pubmed |
pubmed-article:3782301 | pubmed:abstractText | Considerable evidence suggests that Ca2+ modulates endothelial cell metabolic and morphologic responses to mediators of inflammation. We have used the fluorescent Ca2+ indicator, quin2, to monitor endothelial cell cytosolic free Ca2+, [Ca2+]i, in cultured human umbilical vein endothelial cells. Histamine stimulated an increase in [Ca2+]i from a resting level of 111 +/- 4 nM (mean +/- SEM, n = 10) to micromolar levels; maximal and half-maximal responses were elicited by 10(-4) M and 5 X 10(-6) M histamine, respectively. The rise in [Ca2+]i occurred with no detectable latency, attained peak values 15-30 s after addition of stimulus, and decayed to a sustained elevation of [Ca2+]i two- to threefold resting. H1 receptor specificity was demonstrated for the histamine-stimulated changes in [Ca2+]i. Experiments in Ca2+-free medium and in the presence of pyrilamine or the Ca2+ entry blockers Co2+ or Mn2+, indicated that Ca2+ mobilization from intracellular pools accounts for the initial rise, whereas influx of extracellular Ca2+ and continued H1 receptor occupancy are required for sustained elevation of [Ca2+]i. Ionomycin-sensitive intracellular Ca2+ stores were completely depleted by 4 min of exposure to 5 X 10(-6) M histamine. Verapamil or depolarization of endothelial cells in 120 mM K+ did not alter resting or histamine-stimulated [Ca2+]i, suggesting that histamine-elicited changes are not mediated by Ca2+ influx through voltage-gated channels. Endothelial cells grown on polycarbonate filters restricted the diffusion of a trypan blue-albumin complex; histamine (through an H1-selective effect) promoted trypan blue-albumin diffusion with a concentration dependency similar to that for the histamine-elicited rise in [Ca2+]i. Exposure of endothelial cells to histamine (10(-5) M) or ionomycin (10(-7) M) was associated with a decline in endothelial F-actin (relative F-actin content, 0.76 +/- 0.07 vs. 1.00 +/- 0.05; histamine vs. control, P less than 0.05; relative F-actin content, 0.72 +/- 0.06 vs. 1.00 +/- 0.05; ionomycin vs. control, P less than 0.01). The data support a role for cytosolic calcium in the regulation of endothelial shape change and vessel wall permeability in response to histamine. | lld:pubmed |
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pubmed-article:3782301 | pubmed:language | eng | lld:pubmed |
pubmed-article:3782301 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3782301 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:3782301 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:3782301 | pubmed:month | Dec | lld:pubmed |
pubmed-article:3782301 | pubmed:issn | 0021-9525 | lld:pubmed |
pubmed-article:3782301 | pubmed:author | pubmed-author:GallinJ IJI | lld:pubmed |
pubmed-article:3782301 | pubmed:author | pubmed-author:RotrosenDD | lld:pubmed |
pubmed-article:3782301 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:3782301 | pubmed:volume | 103 | lld:pubmed |
pubmed-article:3782301 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:3782301 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:3782301 | pubmed:pagination | 2379-87 | lld:pubmed |
pubmed-article:3782301 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:3782301 | pubmed:year | 1986 | lld:pubmed |
pubmed-article:3782301 | pubmed:articleTitle | Histamine type I receptor occupancy increases endothelial cytosolic calcium, reduces F-actin, and promotes albumin diffusion across cultured endothelial monolayers. | lld:pubmed |
pubmed-article:3782301 | pubmed:publicationType | Journal Article | lld:pubmed |
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