JDS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J. Dairy Sci. 2008. 91:2808-2813. doi:10.3168/jds.2007-0789
© 2008 American Dairy Science Association ®

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Interpretive Summary
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Google Scholar
Right arrow Articles by Bionaz, M.
Right arrow Articles by Varga, G. A.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bionaz, M.
Right arrow Articles by Varga, G. A.

Short Communication: Characterization of Madin-Darby Bovine Kidney Cell Line for Peroxisome Proliferator-Activated Receptors: Temporal Response and Sensitivity to Fatty Acids

M. Bionaz*,1,2, C. R. Baumrucker*, E. Shirk{dagger},3, J. P. Vanden Heuvel{dagger}, E. Block{ddagger} and G. A. Varga*

* Department of Animal Sciences, and
{dagger} Department of Veterinary and Biochemical Sciences, Penn State University, University Park, PA 16801
{ddagger} Arm and Hammer Animal Nutrition Group, Church & Dwight Co. Inc., Princeton, NJ 08543

2 Corresponding author: bionaz{at}uiuc.edu

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 PPAR{alpha} agonist) and rosiglitazone (ROSI, specific PPAR{gamma} agonist). The gene expression of specific PPAR{alpha}-responsive genes such as carnitine palmitoyl transferase-1 (CPT1A) and acetyl coenzyme A oxidase (ACOX1) and of PPAR{gamma}-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 PPAR{alpha} 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 PPAR{alpha}.

Key Words: Madin-Darby bovine kidney cell • peroxisome proliferator-activated receptor • fatty acid • gene expression







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2008 by the American Dairy Science Association ®.