TitleCharacterization of Madin-Darby bovine kidney cell line for peroxisome proliferator-activated receptors: temporal response and sensitivity to fatty acids.
Publication TypeJournal Article
Year of Publication2008
AuthorsBionaz, M, Baumrucker, CR, Shirk, E, Heuvel, JPVanden, Block, E, Varga, GA
JournalJ Dairy Sci
Volume91
Issue7
Pagination2808-13
Date Published2008 Jul
ISSN1525-3198
KeywordsAnimals, Cattle, Cell Line, Energy Metabolism, Gene Expression Regulation, Lipid Metabolism, Peroxisome Proliferator-Activated Receptors, Peroxisome Proliferators, Pyrimidines, Reverse Transcriptase Polymerase Chain Reaction, Thiazolidinediones
Abstract

The peroxisome proliferator-activated receptors (PPAR) are critical for lipid metabolism, and many fatty acids are PPAR agonists. Madin-Darby bovine kidney (MDBK) cells were tested as an in vitro bovine model for PPAR activation, and preliminary evaluation of the effect of fatty acids on bovine PPAR was performed. Cells were treated with Wy-14643 (WY, specific PPARalpha agonist) and rosiglitazone (ROSI, specific PPARgamma agonist). The gene expression of specific PPARalpha-responsive genes such as carnitine palmitoyl transferase-1 (CPT1A) and acetyl coenzyme A oxidase (ACOX1) and of PPARgamma-responsive gene lipoprotein lipase (LPL) were analyzed using real-time reverse transcription PCR. It was found that CPT1A exhibited a significant increase in cells treated with WY, whereas the ACOX1 gene expression was not altered. The LPL gene expression showed an increase in response to ROSI. Interestingly, LPL was almost undetectable in MDBK cells not treated with ROSI. The potency of different fatty acids in activating PPARalpha as assessed by CPT1A mRNA abundance in MDBK cells was also tested. The mRNA of CPT1A (2.5- to 1.4-fold) was significantly increased by fatty acids in the order of palmitate > linolenate > linoleate > conjugated linoleate, and oleate. The results demonstrated MDBK cells to be responsive to PPAR agonists and thus a promising model to evaluate the role of PPAR in bovine cells. In addition, fatty acids were proven to have a different potency in modulating expression of CPT1A through PPARalpha.

DOI10.3168/jds.2007-0789
Alternate JournalJ. Dairy Sci.
PubMed ID18565938