首页 | 本学科首页   官方微博 | 高级检索  
检索        


Phospholipase D in heart: basal activity and stimulation by phorbol esters and aluminum fluoride
Authors:Ruth Lindmar  Konrad Löffelholz
Institution:(1) Department of Pharmacology, University of Mainz, Obere Zahlbacher Strasse 67, W-6500 Mainz, Federal Republic of Germany
Abstract:Summary Evidence for a general role of phospholipase D in signal transduction is accumulating. In the present study, the activity of the enzyme was investigated in heart tissue under basal conditions and after addition of phorbol esters or aluminum fluoride (AlF inf4 sup– ; 10 mM NaF plus 10 mgrM AlCl3). Atria of rats and chickens were incubated with 3H]-myristic acid in order to label preferentially phosphatidylcholine. Under basal conditions, the tissues generated choline and phosphatidic acid (PtdOH), the primary catalytic products of phospholipase D. When 0.5 or 2.0% ethanol was present, 3H]-phosphatidyl-ethanol (PETH) was rapidly formed at the expense of 3H]-PtdOH. This transphosphatidylation reaction is specific for phospholipase D activity. The basal formation of PETH was not inhibited by a Ca2+-free, EGTA-containing medium. - The phorbol ester 4beta-phorbol-12beta,13agr-dibutyrate (PDB), which is known to activate protein kinase C, enhanced the net formation of choline, whereas the inactive 4beta-phorbol-13agr-acetate (PAc) was ineffective. PDB (0.2 mgrM), in contrast to PAc, also increased the formation of 3H]-PtdOH and, in the presence of ethanol, of 3H]-PETH. The PDB-evoked formation of PETH occurred again at the expense of PtdOH. Treshold and maximum effective concentrations of PDB were 10 nM and 0.2–0.6 mgrM, respectively. The effects of PDB on either choline efflux and generation of PETH showed the same Cat+-dependency, i.e., both effects were blocked by a Ca2+-free, EGTA-containing medium, but not by a Ca2+-free medium without EGTA. In protein kinase C-deficient tissue which was prepared by pretreatment with 0.61 mgrM PDB for 27 h, PDB failed to enhance the formation of PtdOH and PETH. - A1F4–, a known activator of G-proteins, increased not only the tissue content of inositol phosphates, but also markedly enhanced choline efflux and formation of 3H]-PtdOH and PETH. In conclusion, in mammalian and avian atria a high phospholipase D activity was found even under basal conditions. The enzyme was stimulated by protein kinase C and presumably by a G protein.Abbreviations IP inositol phosphate - DAG diacylglycerol - PL phospholipase - PtdOH phosphatidic acid - PETH phosphatidylethanol - PDB 4beta-phorbol-12beta,13agr-dibutyrate - PAc 4beta-phorbol-13agr-acetate - AlF inf4 sup– aluminum fluoride - DMSO dimethylsulfoxide Correspondence to K. Löffelholz at the above address
Keywords:Phospholipase D  Protein kinase C  Phorbol ester  Aluminum fluoride  Signal transduction pathways  Heart
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号