Heterogeneity of the Ca2+ sensitivity of secretion in a pituitary gonadotrope cell line and its modulation by protein kinase C and Ca2+

2006 ◽  
Vol 207 (3) ◽  
pp. 668-674 ◽  
Author(s):  
Hui-Sheng Liu ◽  
Zhi-Tao Hu ◽  
Ke-Ming Zhou ◽  
Ya-Ming Jiu ◽  
Hua Yang ◽  
...  
Keyword(s):  
Protein Kinase C ◽  
Protein Kinase ◽  
Cell Line ◽  
Kinase C

Activation of protein kinase C attenuates prostaglandin E2 responses in a colonic cell line

1988 ◽  
Vol 255 (1) ◽  
pp. G27-G32 ◽  
Author(s):  
G. Warhurst ◽  
N. B. Higgs ◽  
M. Lees ◽  
A. Tonge ◽  
L. A. Turnberg
Keyword(s):  
Protein Kinase C ◽  
Protein Kinase ◽  
Adenylate Cyclase ◽  
Prostaglandin E2 ◽  
Cell Line ◽  
Cellular Response ◽  
Short Circuit ◽  
Regulatory Subunit ◽  
Epithelial Cell Line ◽  
Kinase C

We examined the possibility that the protein kinase C pathway may interact with the adenosine 3',5'-cyclic monophosphate (cAMP) pathway in intestinal epithelium by studying the influence of phorbol esters on the response to prostaglandin E2 (PGE2) in a colonic epithelial cell line. Pretreatment of T84 cells with 4 beta-phorbol 12,13-dibutyrate (PDB) markedly attenuated the rise in short-circuit current provoked by PGE2, a receptor-mediated cAMP agonist. The EC50 of this effect was 52 nM PDB with a half time of 4-6 min. The responses to nonreceptor-mediated agonists, forskolin and dibutyryl cAMP, were unaffected by phorbol ester. PDB also reduced the ability of PGE2 to stimulate adenylate cyclase activity in these cells. The accumulation of cAMP in response to PGE2 was inhibited by PDB (EC50 38 nM), an effect mimicked by the diacylglycerol analogue 1-oleoyl-2-acetyl-sn-glycerol. In addition, PGE2 stimulation of adenylate cyclase in membranes from PDB-treated cells was reduced by 30-40%. Inhibition was not mediated via the catalytic or regulatory subunit of the adenylate cyclase, implying an action involving desensitization of PGE2 receptors. These results provide evidence of a complex interrelationship between protein kinase C- and cAMP-mediated pathways that might be important in regulating the cellular response to secretagogues.

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