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PHORBOL ESTERS ENHANCE EXOCYTOSIS FROM CHROMAFFIN CELLS BY 2 MECHANISMS
被引:30
|
作者
:
BITTNER, MA
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan
BITTNER, MA
HOLZ, RW
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan
HOLZ, RW
机构
:
[1]
Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan
来源
:
JOURNAL OF NEUROCHEMISTRY
|
1990年
/ 54卷
/ 01期
关键词
:
Catecholamine;
Chromaffin cell;
Digitonin;
Exocytosis;
permeabilized;
Phorbol ester;
Protein kinase C;
D O I
:
10.1111/j.1471-4159.1990.tb13302.x
中图分类号
:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号
:
071010 ;
081704 ;
摘要
:
Abstract: Treatment with phorbol esters such as 12‐O‐tet‐radecanoylphorbol acetate (TPA) rapidly enhances [3H]norepinephrine secretion from digitonin‐permeabilized adrenal chromaffin cells. When TPA treatment was prolonged for several hours, a second distinct enhancing effect was observed. This later enhancement was most prominent at intracellular Ca2+ concentrations of 3–30 μM, and did not require the continued presence of membrane‐bound protein kinase C for its expression. The effect could be elicited by as little as 30‐min exposure to TPA, followed by several hours in TPA‐free medium. This effect of TPA was blocked by actinomycin D and cycloheximide, indicating a requirement for RNA and protein synthesis. Similar effects were seen when intact cells that had been pretreated with TPA were stimulated to secrete by depolarizing concentrations of K+. Thus, protein kinase C enhances secretion by two mechanisms. One is rapid and probably reflects the effects of immediate protein phosphorylation. The other occurs over several hours and requires gene transcription and protein synthesis. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
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页码:205 / 210
页数:6
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