• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to project page

1996 Fiscal Year Final Research Report Summary

Mechanisms of Protein Kinase C Activatic by Lipid Peroxidation and its Biological Significance

Research Project

Project/Area Number 07457587
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Experimental pathology
Research InstitutionTokai university

Principal Investigator

WATANABE Keiichi  Tokai University School of Medicine Professor, 医学部, 教授 (00055865)

Co-Investigator(Kenkyū-buntansha) YAMAMOTO Yorihiro  Research Center for Advanced Sciene and Associate Professor Technology The Unive, 先端科学技術研究センター, 助教授 (60134475)
SATO Shinkichi  Tokai University School of Medicine Assistant Professor, 医学部, 講師 (80119677)
TAKEKOSHI Susumu  Tokyai University School of Medicine Assistant Resarcher, 医学部, 助手 (70216878)
Project Period (FY) 1995 – 1996
KeywordsProtein Kinase C / Diacylglycerol / Oxidized diacylglycerol / Phorbol ester (PMA) / Alzheimer's disease / 微細管異常 / tau / map-2
Research Abstract

It is well known fact that cell membrane lipids undergo lipid peroxidation by the attacks of oxygen and other various free radicals, and cell injuries of varying degree pursue. It has, however, not yet proved that lipid peroxides of certain very specific substances (lipids) prohibit or activate very specific cell reactions properly. Most of protein kinase C (PKC) are known to be activated by various lipids, especially diacylglycerols (DAG) whose characteristic PKC activation has been attracting many investigators' attentions. Since DAG contains oxidatively vulnerable polyunsaturated fatty acids, we presumed that hydroperoxidized DAG (DAG-OOH) could be produced through membrane lipid peroxidation. In this regards, we tried and succeeded to prepare the DAG-OOH from soybean phosphatidylcholine through the enzymatic cleavage to form 1,2-DAG (dilinorein) and pursuing aerobic oxidation. And then, we applied these DAG,DAG-OOH and PMA (phorbol ester), which is known to be a general and most ef … More fective PKC activator, on PKC purified from rat brains. As a result, DAG-OOH exhibited 3 fold stronger activation than that of the natural DAG,which was almost comparable to that of PMA.Interestingly, hydroperoxidized form of artificially prepared 1,3-DAG (natural one is unexceptionally 1,2-DAG) did not show any particular PKC activation. DAG and its oxidized forms used in this experiment were dilinolein (LL-DAG) obtained from soybeans. In animal tissues, however, palmitate (P), linoleate (L) -DAG,stearate (S), L-DAG and so on must be commonly distributed. We applied hydroperoxidized forms of those series of DAGs on the rat PKC and P,L- and S,L-DAG-OOHs were found to be similarly effective as L,L-DAG-OOH.
Reportedly, microtubule associated proteins (tau, map 2 etc.) phosphorylated excessively by PMA activated PKC induce microtubule disassembly which gives finally rise to "neurofibrillary tangles" like lesions in human or animal cultures cells. We applied DAG,DAG-OOH (both 1,2- and 1,3- forms) and PMA on cultured neuronal cells (cultured from rat fetal brain and NGF stimulated PC 12 cells), and the most conspicuous structural changes (chained beads like lesion which may well be due to microtubule abnormality) were provoked by 1,2-DAG-OOH but not by 1,3-DAG-OOH.This evidence may well e an important clue to elucidate the pathogenesis of neurodegenerative diseases such as Alzheimer's disease, for DAG-OOH,differing from an artificial product PMA,is biologically accessible substance. Less

  • Research Products

    (2 results)

All Other

All Publications (2 results)

  • [Publications] S.Takekoshi et al.: "Activation of protein kinase C by oxidized diacylglycerols." Biochemical and Biophysical Research Communications.217(2). 654-660 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Susumu Takekoshi, Yasuhiro Kambayashi, Hidetaka Nagata, Tetsuo Takagi, Keiichi Watanabe: "Activation of protein kinase C by oxidized diacylglycerols" Biochemical and Biophysical Reserch Communication. 217 (2). 654-660 (1995)

    • Description
      「研究成果報告書概要(欧文)」より

URL: 

Published: 1999-03-09  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi