Role of peroxisome proliferator-activated receptor-α on the synthesis of monounsaturated fatty acids in goat mammary epithelial cells.
Animals
Epithelial Cells
/ metabolism
Fatty Acid-Binding Proteins
Fatty Acids
/ metabolism
Fatty Acids, Monounsaturated
/ metabolism
Female
Gene Expression Regulation
Goats
Lipid Metabolism
Lipogenesis
/ genetics
Mammary Glands, Animal
/ metabolism
PPAR alpha
/ metabolism
Peroxisome Proliferators
/ metabolism
Sterol Regulatory Element Binding Protein 1
Triglycerides
/ metabolism
Up-Regulation
PPAR
gene expression
lactation
milk fat
ruminant
Journal
Journal of animal science
ISSN: 1525-3163
Titre abrégé: J Anim Sci
Pays: United States
ID NLM: 8003002
Informations de publication
Date de publication:
01 Mar 2020
01 Mar 2020
Historique:
received:
03
01
2020
accepted:
14
02
2020
pubmed:
19
2
2020
medline:
19
8
2020
entrez:
19
2
2020
Statut:
ppublish
Résumé
A key member of the nuclear receptor superfamily is the peroxisome proliferator-activated receptor alpha (PPARA) isoform, which in nonruminants is closely associated with fatty acid oxidation. Whether PPARA plays a role in milk fatty acid synthesis in ruminants is unknown. The main objective of the present study was to use primary goat mammary epithelial cells (GMEC) to activate PPARA via the agonist WY-14643 (WY) or to silence it via transfection of small-interfering RNA (siRNA). Three copies of the peroxisome proliferator-activated receptor response element (PPRE) contained in a luciferase reporter vector were transfected into GMEC followed by incubation with WY at 0, 10, 20, 30, 50, or 100 µM. A dose of 50 µM WY was most effective at activating PPRE without influencing PPARA mRNA abundance. Transfecting siRNA targeting PPARA decreased its mRNA abundance to 20% and protein level to 50% of basal levels. Use of WY upregulated FASN, SCD1, ACSL1, DGAT1, FABP4, and CD36 (1.1-, 1.5-, 2-, 1.4-, 1.5-, and 5-fold, respectively), but downregulated DGAT2 and PGC1A (-20% and -40%, respectively) abundance. In contrast, triacylglycerol concentration decreased and the content and desaturation index of C16:1 and C18:1 increased. Thus, activation of PPARA via WY appeared to channel fatty acids away from esterification. Knockdown of PPARA via siRNA downregulated ACACA, SCD1, AGPAT6, CD36, HSL, and SREBF1 (-43%, -67%, -16%, -56%, -26%, and -29%, respectively), but upregulated ACSL1, DGAT2, FABP3, and PGC1A (2-, 1.4-, 1.3-, and 2.5-fold, respectively) mRNA abundance. A decrease in the content and desaturation index of C16:1 and C18:1 coupled with an increase in triacylglycerol content accompanied those effects at the mRNA level. Overall, data suggest that PPARA could promote the synthesis of MUFA in GMEC through its effects on mRNA abundance of genes related to fatty acid synthesis, oxidation, transport, and triacylglycerol synthesis.
Identifiants
pubmed: 32067038
pii: 5739815
doi: 10.1093/jas/skaa062
pmc: PMC7070155
pii:
doi:
Substances chimiques
FABP4 protein, human
0
Fatty Acid-Binding Proteins
0
Fatty Acids
0
Fatty Acids, Monounsaturated
0
PPAR alpha
0
Peroxisome Proliferators
0
SREBF1 protein, human
0
Sterol Regulatory Element Binding Protein 1
0
Triglycerides
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© The Author(s) 2020. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
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