Fatty acid regulation of liver X receptors (LXR) and peroxisome proliferator-activated receptor α (PPARα) in HEK293 cells

Anjali Pawar, Jinghua Xu, Erik Jerks, David J. Mangelsdorf, Donald B. Jump

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Abstract

Fatty acids bind to and regulate the activity of peroxisome proliferator-activated (PPAR) and liver X receptors (LXR). However, the role lipid metabolism plays in the control of intracellular fatty acid ligands is poorly understood. We have identified two strains of HEK293 cells that display differences in fatty acid regulation of nuclear receptors. Using full-length and Gal4-LBD chimeric receptors in functional assays, 20:4,n6 induced PPARα activity ∼2.2-fold and suppressed LXRα activity by 80% (ED50 μ25-50 μM) in HEK293-E (early passage) cells but had no effect on PPARα or LXRα receptor activity in HEK293-L (late passage) cells. LXRβ was insensitive to fatty acid regulation in both HEK293 strains. Metabolic labeling studies using [14C]20:4,n6 (at 100 μM) indicated that the uptake of 20:4,n6 and its assimilation into triacylglycerol, diacylglycerol, and polar lipids revealed no difference between the two strains. Such treatment increased total cellular 20:4,n6 (∼11-fold) and its elongation product, 22:4,n6 (∼3.6-fold), within 6 h. Non-esterified 20:4,n6 and 22:4,n6 represented ≤3% of the total cellular 20:4,n6 and 22-4,n6. In HEK293-E cells, non-esterified 20:4,n6 and 22-4,n6 increased 8- and 18-fold, respectively, by 6 h and was sustained at that level for 24 h. In HEK293-L cells, non-esterified 20:4,n6 also increased (5-fold) at 6 h but fell by 70% within 24 h. In contrast to HEK293-E cells, non-esterified 22:4,n6 did not accumulate in HEK293-L cells. Functional assays showed that 22:4,n6 was ∼2-fold more effective than 20: 4,n6 at inhibiting oxysterol-induced LXRα activity in HEK293-E cells, but had no effect on LXRα activity in HEK293-L cells. Taken together, these findings demonstrate that the rate of assimilation of exogenously added fatty acids and their metabolites into complex lipids plays an important role in regulating PPARα and LXRα activity.

Original languageEnglish (US)
Pages (from-to)39243-39250
Number of pages8
JournalJournal of Biological Chemistry
Volume277
Issue number42
DOIs
StatePublished - Oct 18 2002

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Peroxisome Proliferator-Activated Receptors
HEK293 Cells
Liver
Fatty Acids
Assays
Peroxisome Proliferators
Lipids
Diglycerides
Cytoplasmic and Nuclear Receptors
Metabolites
Liver X Receptors
Lipid Metabolism
Labeling
Elongation
Triglycerides
Ligands

ASJC Scopus subject areas

  • Biochemistry

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Fatty acid regulation of liver X receptors (LXR) and peroxisome proliferator-activated receptor α (PPARα) in HEK293 cells. / Pawar, Anjali; Xu, Jinghua; Jerks, Erik; Mangelsdorf, David J.; Jump, Donald B.

In: Journal of Biological Chemistry, Vol. 277, No. 42, 18.10.2002, p. 39243-39250.

Research output: Contribution to journalArticle

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abstract = "Fatty acids bind to and regulate the activity of peroxisome proliferator-activated (PPAR) and liver X receptors (LXR). However, the role lipid metabolism plays in the control of intracellular fatty acid ligands is poorly understood. We have identified two strains of HEK293 cells that display differences in fatty acid regulation of nuclear receptors. Using full-length and Gal4-LBD chimeric receptors in functional assays, 20:4,n6 induced PPARα activity ∼2.2-fold and suppressed LXRα activity by 80{\%} (ED50 μ25-50 μM) in HEK293-E (early passage) cells but had no effect on PPARα or LXRα receptor activity in HEK293-L (late passage) cells. LXRβ was insensitive to fatty acid regulation in both HEK293 strains. Metabolic labeling studies using [14C]20:4,n6 (at 100 μM) indicated that the uptake of 20:4,n6 and its assimilation into triacylglycerol, diacylglycerol, and polar lipids revealed no difference between the two strains. Such treatment increased total cellular 20:4,n6 (∼11-fold) and its elongation product, 22:4,n6 (∼3.6-fold), within 6 h. Non-esterified 20:4,n6 and 22:4,n6 represented ≤3{\%} of the total cellular 20:4,n6 and 22-4,n6. In HEK293-E cells, non-esterified 20:4,n6 and 22-4,n6 increased 8- and 18-fold, respectively, by 6 h and was sustained at that level for 24 h. In HEK293-L cells, non-esterified 20:4,n6 also increased (5-fold) at 6 h but fell by 70{\%} within 24 h. In contrast to HEK293-E cells, non-esterified 22:4,n6 did not accumulate in HEK293-L cells. Functional assays showed that 22:4,n6 was ∼2-fold more effective than 20: 4,n6 at inhibiting oxysterol-induced LXRα activity in HEK293-E cells, but had no effect on LXRα activity in HEK293-L cells. Taken together, these findings demonstrate that the rate of assimilation of exogenously added fatty acids and their metabolites into complex lipids plays an important role in regulating PPARα and LXRα activity.",
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AU - Mangelsdorf, David J.

AU - Jump, Donald B.

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N2 - Fatty acids bind to and regulate the activity of peroxisome proliferator-activated (PPAR) and liver X receptors (LXR). However, the role lipid metabolism plays in the control of intracellular fatty acid ligands is poorly understood. We have identified two strains of HEK293 cells that display differences in fatty acid regulation of nuclear receptors. Using full-length and Gal4-LBD chimeric receptors in functional assays, 20:4,n6 induced PPARα activity ∼2.2-fold and suppressed LXRα activity by 80% (ED50 μ25-50 μM) in HEK293-E (early passage) cells but had no effect on PPARα or LXRα receptor activity in HEK293-L (late passage) cells. LXRβ was insensitive to fatty acid regulation in both HEK293 strains. Metabolic labeling studies using [14C]20:4,n6 (at 100 μM) indicated that the uptake of 20:4,n6 and its assimilation into triacylglycerol, diacylglycerol, and polar lipids revealed no difference between the two strains. Such treatment increased total cellular 20:4,n6 (∼11-fold) and its elongation product, 22:4,n6 (∼3.6-fold), within 6 h. Non-esterified 20:4,n6 and 22:4,n6 represented ≤3% of the total cellular 20:4,n6 and 22-4,n6. In HEK293-E cells, non-esterified 20:4,n6 and 22-4,n6 increased 8- and 18-fold, respectively, by 6 h and was sustained at that level for 24 h. In HEK293-L cells, non-esterified 20:4,n6 also increased (5-fold) at 6 h but fell by 70% within 24 h. In contrast to HEK293-E cells, non-esterified 22:4,n6 did not accumulate in HEK293-L cells. Functional assays showed that 22:4,n6 was ∼2-fold more effective than 20: 4,n6 at inhibiting oxysterol-induced LXRα activity in HEK293-E cells, but had no effect on LXRα activity in HEK293-L cells. Taken together, these findings demonstrate that the rate of assimilation of exogenously added fatty acids and their metabolites into complex lipids plays an important role in regulating PPARα and LXRα activity.

AB - Fatty acids bind to and regulate the activity of peroxisome proliferator-activated (PPAR) and liver X receptors (LXR). However, the role lipid metabolism plays in the control of intracellular fatty acid ligands is poorly understood. We have identified two strains of HEK293 cells that display differences in fatty acid regulation of nuclear receptors. Using full-length and Gal4-LBD chimeric receptors in functional assays, 20:4,n6 induced PPARα activity ∼2.2-fold and suppressed LXRα activity by 80% (ED50 μ25-50 μM) in HEK293-E (early passage) cells but had no effect on PPARα or LXRα receptor activity in HEK293-L (late passage) cells. LXRβ was insensitive to fatty acid regulation in both HEK293 strains. Metabolic labeling studies using [14C]20:4,n6 (at 100 μM) indicated that the uptake of 20:4,n6 and its assimilation into triacylglycerol, diacylglycerol, and polar lipids revealed no difference between the two strains. Such treatment increased total cellular 20:4,n6 (∼11-fold) and its elongation product, 22:4,n6 (∼3.6-fold), within 6 h. Non-esterified 20:4,n6 and 22:4,n6 represented ≤3% of the total cellular 20:4,n6 and 22-4,n6. In HEK293-E cells, non-esterified 20:4,n6 and 22-4,n6 increased 8- and 18-fold, respectively, by 6 h and was sustained at that level for 24 h. In HEK293-L cells, non-esterified 20:4,n6 also increased (5-fold) at 6 h but fell by 70% within 24 h. In contrast to HEK293-E cells, non-esterified 22:4,n6 did not accumulate in HEK293-L cells. Functional assays showed that 22:4,n6 was ∼2-fold more effective than 20: 4,n6 at inhibiting oxysterol-induced LXRα activity in HEK293-E cells, but had no effect on LXRα activity in HEK293-L cells. Taken together, these findings demonstrate that the rate of assimilation of exogenously added fatty acids and their metabolites into complex lipids plays an important role in regulating PPARα and LXRα activity.

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