rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
1
|
pubmed:dateCreated |
1985-2-4
|
pubmed:abstractText |
The mitogenic response of human peripheral blood lymphocytes to the lectin concanavalin A (conA) is inhibited by micromolar concentrations of CdCl2. This inhibition is partially relieved by an increase in the external Ca2+ concentration (from 0.6 to 2.2 mM). The initial rate of conA-induced 45Ca2+ influx is unaltered by CdCl2, although the level of 45Ca2+ accumulation increases. The basal rate of 45Ca2+ entry is not measurably disturbed by CdCl2 (100 microM). The steady-state efflux of 45Ca2+ and the calmodulin-activated (Ca2+ + Mg2+)-ATPase activity of erythrocyte ghosts are inhibited by CdCl2 (10 microM). Thus, the mechanism behind the Cd2+-induced suppression of the mitogenic response to conA is not due to alteration of mitogen-stimulated Ca2+ influx. We suggest that Cd2+ competes with Ca2+ for intracellular Ca2+-binding molecules, such as calmodulin, essential for the induction of cell proliferation.
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pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0014-4827
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
156
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
191-7
|
pubmed:dateRevised |
2010-11-18
|
pubmed:meshHeading |
pubmed-meshheading:3155505-Biological Transport, Active,
pubmed-meshheading:3155505-Ca(2+) Mg(2+)-ATPase,
pubmed-meshheading:3155505-Cadmium,
pubmed-meshheading:3155505-Cadmium Chloride,
pubmed-meshheading:3155505-Calcium,
pubmed-meshheading:3155505-Calcium-Transporting ATPases,
pubmed-meshheading:3155505-Cell Division,
pubmed-meshheading:3155505-Cells, Cultured,
pubmed-meshheading:3155505-Concanavalin A,
pubmed-meshheading:3155505-Erythrocyte Membrane,
pubmed-meshheading:3155505-Humans,
pubmed-meshheading:3155505-Lymphocyte Activation,
pubmed-meshheading:3155505-Lymphocytes
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pubmed:year |
1985
|
pubmed:articleTitle |
Effects of Cd2+ upon Ca2+ fluxes and proliferation in concanavalin A-stimulated lymphocytes.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|