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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0006639,
umls-concept:C0015127,
umls-concept:C0033634,
umls-concept:C0034693,
umls-concept:C0034721,
umls-concept:C0040715,
umls-concept:C0596235,
umls-concept:C0599718,
umls-concept:C0599813,
umls-concept:C0599893,
umls-concept:C0935597,
umls-concept:C1314792,
umls-concept:C1383501,
umls-concept:C1522702,
umls-concept:C1880497,
umls-concept:C1996904
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pubmed:issue |
1 Pt 1
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pubmed:dateCreated |
1988-8-11
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pubmed:abstractText |
We investigated the relationships between changes in cytosolic free Ca2+ ([Ca2+]i) and amylase secretion in dispersed rat pancreatic acini. Although 10 pM caerulein did not raise [Ca2+]i, higher concentrations (1 nM) of the peptide elicited a prompt, marked, but transient (2-3 min) elevation of [Ca2+]i. Both concentrations of caerulein caused an almost identical release of amylase over a 30-min period. To investigate the mechanism(s) underlying Ca2+-independent secretion, we measured the effect of the secretagogue on protein kinase C activity and found that both caerulein concentrations caused a significant translocation of protein kinase C from the cytosolic to the microsomal fraction. Because 1 nM caerulein induced a greater enzyme secretion than 10 pM caerulein during the first 2-5 min of stimulation, we explored further the role of [Ca2+]i transients during the first minutes of secretion. Addition of ionomycin in the presence of 10 pM caerulein resulted in a rise in [Ca2+]i and enhanced secretion as a result of caerulein in a near additive fashion during the first 2 min of stimulation. Second, we pretreated acini for 5 min with 1 microM 12-O-tetradecanoylphorbol-13-acetate. This maneuver inhibited both caerulein-induced inositol trisphosphate formation and [Ca2+]i elevation. These findings were paralleled by a similar inhibition of caerulein-stimulated amylase release only during the first 5 min of secretion. These results indicate that 1) caerulein can stimulate amylase secretion independently of a concomitant [Ca2+]i rise, possibly by activation of protein kinase C, and 2) an elevation of [Ca2+]i serves as a trigger to enhance amylase release only during the initial phase of secretion.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Amylases,
http://linkedlifedata.com/resource/pubmed/chemical/Benzofurans,
http://linkedlifedata.com/resource/pubmed/chemical/Caerulein,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Fura-2,
http://linkedlifedata.com/resource/pubmed/chemical/Inositol 1,4,5-Trisphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Inositol Phosphates,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C,
http://linkedlifedata.com/resource/pubmed/chemical/Tetradecanoylphorbol Acetate
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0002-9513
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
255
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
G33-9
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:2455450-Amylases,
pubmed-meshheading:2455450-Animals,
pubmed-meshheading:2455450-Benzofurans,
pubmed-meshheading:2455450-Caerulein,
pubmed-meshheading:2455450-Calcium,
pubmed-meshheading:2455450-Fura-2,
pubmed-meshheading:2455450-Inositol 1,4,5-Trisphosphate,
pubmed-meshheading:2455450-Inositol Phosphates,
pubmed-meshheading:2455450-Male,
pubmed-meshheading:2455450-Pancreas,
pubmed-meshheading:2455450-Protein Kinase C,
pubmed-meshheading:2455450-Rats,
pubmed-meshheading:2455450-Rats, Inbred Strains,
pubmed-meshheading:2455450-Tetradecanoylphorbol Acetate
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pubmed:year |
1988
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pubmed:articleTitle |
Caerulein causes translocation of protein kinase C in rat acini without increasing cytosolic free Ca2+.
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pubmed:affiliation |
Institut de Biochimie Clinique, University of Geneva, Switzerland.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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