View : 1019 Download: 0

Full metadata record

DC Field Value Language
dc.contributor.author전길자*
dc.contributor.author배윤수*
dc.contributor.author고수영*
dc.contributor.author한소엽*
dc.contributor.author임진경*
dc.date.accessioned2016-08-28T11:08:31Z-
dc.date.available2016-08-28T11:08:31Z-
dc.date.issued2003*
dc.identifier.issn1015-8987*
dc.identifier.otherOAK-1727*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/219337-
dc.description.abstractA factor stimulating a mitogenic activity of peritoneal macrophages is purified from bovine udder. It is identified as a triglyceride, 1-palmitoyl-2-linoleoyl-3-acetyl-rac-glycerol (rac-MADG). In this study, its enantiomers, R-(+)-and S-(-)-1-palmitoyl-2-linoleoyl-3-acetylglycerol (R-(+)-MADG, S-(-)-MADG) are synthesized. Among them, R-(+)-MADG enantiomer turns out to increase a mitogenic activity in mouse peritoneal macrophages. Also, (S)-(-)-MADG shows a low mitogenic activity. Treatment of a macrophage with R-(+)-MADG increases reactive oxygen species (ROS). Furthermore, treatment of macrophages with antioxidant, N-acetyl-L-cysteine (NAC), suppresses the R-(+)-MADG-dependent macrophage proliferation. Results show that the generation of ROS induces in R-(+)-MADG-dependent cell signaling. Treatment of a macrophage with R-(+)-MADG increases the activity of protein kinase C (PKC). Treatment of macrophages with calphostin C inhibits R-(+)-MADG-induced macrophage proliferation. Results suggest that R-(+)-MADG enhances the activity of protein kinase C (PKC) and stimulates the macrophage growth. In conclusions, R-(+)-MADG accelerates the production of ROS and increases the activity of PKC to eventually stimulate macrophage cell growth. The existence of rac-MADG in bovine udder and milk provides passive protection for the neonate and immunostimulatory capabilities. Copyright © 2003 S. Karger AG, Basel.*
dc.languageEnglish*
dc.titleTriacylglycerol, 1-palmitoyl-2-linoleoyl-3-acetyl-rac-glycerol isolated from bovine udder and its synthetic enantiomer can potentiate the mitogenic activity for mouse peritoneal macrophages*
dc.typeArticle*
dc.relation.issue6*
dc.relation.volume13*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage415*
dc.relation.lastpage422*
dc.relation.journaltitleCellular Physiology and Biochemistry*
dc.identifier.doi10.1159/000075129*
dc.identifier.wosidWOS:000186684400010*
dc.identifier.scopusid2-s2.0-0345689348*
dc.author.googleSuh J.S.*
dc.author.googleKwon J.*
dc.author.googleEun J.S.*
dc.author.googleLee Y.J.*
dc.author.googleLimb J.K.*
dc.author.googleKo S.Y.*
dc.author.googleHan S.Y.*
dc.author.googleBae Y.S.*
dc.author.googleJhon G.J.*
dc.contributor.scopusid전길자(6701488476)*
dc.contributor.scopusid배윤수(15031067200)*
dc.contributor.scopusid고수영(7403325351)*
dc.contributor.scopusid한소엽(7405944194)*
dc.contributor.scopusid임진경(7003530407)*
dc.date.modifydate20240415133331*
Appears in Collections:
자연과학대학 > 화학·나노과학전공 > Journal papers
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML


qrcode

BROWSE