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Identification and distribution of endoplasmic reticulum iPLA2.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2005 Feb 04; Vol. 327 (1), pp. 287-93. - Publication Year :
- 2005
-
Abstract
- Our laboratory demonstrated that endoplasmic reticulum iPLA2 (ER-iPLA2) activity protects renal cells from oxidant-induced cell death and lipid peroxidation. The goals of this study were to determine the PLA2 isoform(s) responsible for ER-iPLA2 activity in different species and tissues. ER-iPLA2 activity was observed in microsomes from rabbit and rat kidney, heart, and brain as well as in human kidney (Caki-1 and HEK293) and glioblastoma (A172) cell lines. Reverse transcriptase-polymerase chain reaction results demonstrated the presence of iPLA2gamma (group VIB PLA2) message in all tissues tested. Immunoblot analysis and PLA2 inhibitor studies with methyl arachidonyl fluorophosphonate and enantiomers of bromoenol lactone demonstrated that the ER-iPLA2 in rabbit kidney and heart and rat kidney is iPLA2gamma. These results demonstrate the expression of ER-iPLA2gamma (group VIB) across species and tissues, and suggest that iPLA2gamma may play critical roles in oxidant-induced cell injury.
- Subjects :
- Amino Acid Sequence
Animals
Arachidonic Acids pharmacology
Cell Line
Endoplasmic Reticulum genetics
Enzyme Inhibitors pharmacology
Female
Group VI Phospholipases A2
Humans
Kidney enzymology
Male
Microsomes enzymology
Molecular Sequence Data
Myocardium enzymology
Naphthalenes pharmacology
Organ Specificity
Organophosphonates pharmacology
Phospholipases A antagonists & inhibitors
Phospholipases A chemistry
Phospholipases A genetics
Phospholipases A2
Protein Isoforms antagonists & inhibitors
Protein Isoforms genetics
Protein Isoforms metabolism
Pyrones pharmacology
RNA, Messenger genetics
RNA, Messenger metabolism
Rabbits
Rats
Sequence Alignment
Sequence Homology
Species Specificity
Endoplasmic Reticulum enzymology
Phospholipases A metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 327
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 15629460
- Full Text :
- https://doi.org/10.1016/j.bbrc.2004.12.016