Induction of CD36 expression by oxidized LDL and IL-4 by a common signaling pathway dependent on protein kinase C and PPAR-γ
CD36, a class B scavenger receptor, is a macrophage receptor for oxidized low density lipoprotein (OxLDL) and may play a critical role in atherosclerotic foam cell formation. We have previously demonstrated that OxLDL, macrophage-colony stimulating factor (M-CSF), and interleukin-4 (IL-4) enhanced e...
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| Format: | Article |
| Language: | English |
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Elsevier
2000-05-01
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| Series: | Journal of Lipid Research |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S0022227520323774 |
| _version_ | 1818602112309788672 |
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| author | Jianwei Feng Jihong Han S. Freida A. Pearce Roy L. Silverstein Antonio M. Gotto, Jr. David.P. Hajjar Andrew C. Nicholson |
| author_facet | Jianwei Feng Jihong Han S. Freida A. Pearce Roy L. Silverstein Antonio M. Gotto, Jr. David.P. Hajjar Andrew C. Nicholson |
| author_sort | Jianwei Feng |
| collection | DOAJ |
| description | CD36, a class B scavenger receptor, is a macrophage receptor for oxidized low density lipoprotein (OxLDL) and may play a critical role in atherosclerotic foam cell formation. We have previously demonstrated that OxLDL, macrophage-colony stimulating factor (M-CSF), and interleukin-4 (IL-4) enhanced expression of CD36. The effect of OxLDL on CD36 is due, in part, to its ability to activate the transcription factor, PPAR-γ (peroxisome proliferator activated receptor-γ). Other PPAR-γ ligands (15-deoxyΔ12,14 prostaglandin J2 (15d-PGJ2) and the thiazolidinedione class of antidiabetic drugs) also increase CD36 expression. We have now evaluated signaling pathways involved in the induction of CD36. Treatment of RAW264.7 cells (a murine macrophage cell line) with protein kinase C (PKC) activators (diacylglycerol and ingenol) up-regulated CD36 mRNA expression. Specific inhibitors of PKC reduced CD36 expression in a time-dependent manner, while protein kinase A (PKA) and cyclic AMP agonists had no effect on CD36 mRNA expression. PKC inhibitors reduced basal expression of CD36 and blocked induction of CD36 mRNA by 15d-PGJ2, OxLDL and IL-4. In addition, PKC inhibitors decreased both PPAR-γ mRNA and protein expression and blocked induction of CD36 protein surface expression by OxLDL and 15d-PGJ2 in human monocytes, as determined by FACS. 15d-PGJ2 had no effect on translocation of PKC-α from the cytosol to the plasma membrane.These results demonstrate that two divergent physiological or pathophysiological agonists utilize a common pathway to up-regulate of CD36 gene expression. This pathway involves initial activation of PKC with subsequent PPAR-γ activation. Defining these signaling pathways is critical for understanding and modulating expression of this scavenger receptor pathway.—Feng, J., J. Han, S. F. A. Pearce, R. L. Silverstein, A. M. Gotto, Jr., D. P. Hajjar, and A. C. Nicholson. Induction of CD36 expression by oxidized LDL and IL-4 by a common signaling pathway dependent on protein kinase C and PPAR-γ. J. Lipid Res. 2000. 41: 688–696. |
| first_indexed | 2024-12-16T13:02:06Z |
| format | Article |
| id | doaj.art-d1110f33086d435e935de2852cab6249 |
| institution | Directory Open Access Journal |
| issn | 0022-2275 |
| language | English |
| last_indexed | 2024-12-16T13:02:06Z |
| publishDate | 2000-05-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Journal of Lipid Research |
| spelling | doaj.art-d1110f33086d435e935de2852cab62492022-12-21T22:30:48ZengElsevierJournal of Lipid Research0022-22752000-05-01415688696Induction of CD36 expression by oxidized LDL and IL-4 by a common signaling pathway dependent on protein kinase C and PPAR-γJianwei Feng0Jihong Han1S. Freida A. Pearce2Roy L. Silverstein3Antonio M. Gotto, Jr.4David.P. Hajjar5Andrew C. Nicholson6Medicine, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10021Departments of Pathology, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10021Medicine, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10021Medicine, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10021Medicine, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10021Departments of Pathology, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10021To whom correspondence should be addressed.; Departments of Pathology, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10021CD36, a class B scavenger receptor, is a macrophage receptor for oxidized low density lipoprotein (OxLDL) and may play a critical role in atherosclerotic foam cell formation. We have previously demonstrated that OxLDL, macrophage-colony stimulating factor (M-CSF), and interleukin-4 (IL-4) enhanced expression of CD36. The effect of OxLDL on CD36 is due, in part, to its ability to activate the transcription factor, PPAR-γ (peroxisome proliferator activated receptor-γ). Other PPAR-γ ligands (15-deoxyΔ12,14 prostaglandin J2 (15d-PGJ2) and the thiazolidinedione class of antidiabetic drugs) also increase CD36 expression. We have now evaluated signaling pathways involved in the induction of CD36. Treatment of RAW264.7 cells (a murine macrophage cell line) with protein kinase C (PKC) activators (diacylglycerol and ingenol) up-regulated CD36 mRNA expression. Specific inhibitors of PKC reduced CD36 expression in a time-dependent manner, while protein kinase A (PKA) and cyclic AMP agonists had no effect on CD36 mRNA expression. PKC inhibitors reduced basal expression of CD36 and blocked induction of CD36 mRNA by 15d-PGJ2, OxLDL and IL-4. In addition, PKC inhibitors decreased both PPAR-γ mRNA and protein expression and blocked induction of CD36 protein surface expression by OxLDL and 15d-PGJ2 in human monocytes, as determined by FACS. 15d-PGJ2 had no effect on translocation of PKC-α from the cytosol to the plasma membrane.These results demonstrate that two divergent physiological or pathophysiological agonists utilize a common pathway to up-regulate of CD36 gene expression. This pathway involves initial activation of PKC with subsequent PPAR-γ activation. Defining these signaling pathways is critical for understanding and modulating expression of this scavenger receptor pathway.—Feng, J., J. Han, S. F. A. Pearce, R. L. Silverstein, A. M. Gotto, Jr., D. P. Hajjar, and A. C. Nicholson. Induction of CD36 expression by oxidized LDL and IL-4 by a common signaling pathway dependent on protein kinase C and PPAR-γ. J. Lipid Res. 2000. 41: 688–696.http://www.sciencedirect.com/science/article/pii/S0022227520323774CD36macrophagescavenger receptorPKCPPAR-g |
| spellingShingle | Jianwei Feng Jihong Han S. Freida A. Pearce Roy L. Silverstein Antonio M. Gotto, Jr. David.P. Hajjar Andrew C. Nicholson Induction of CD36 expression by oxidized LDL and IL-4 by a common signaling pathway dependent on protein kinase C and PPAR-γ Journal of Lipid Research CD36 macrophage scavenger receptor PKC PPAR-g |
| title | Induction of CD36 expression by oxidized LDL and IL-4 by a common signaling pathway dependent on protein kinase C and PPAR-γ |
| title_full | Induction of CD36 expression by oxidized LDL and IL-4 by a common signaling pathway dependent on protein kinase C and PPAR-γ |
| title_fullStr | Induction of CD36 expression by oxidized LDL and IL-4 by a common signaling pathway dependent on protein kinase C and PPAR-γ |
| title_full_unstemmed | Induction of CD36 expression by oxidized LDL and IL-4 by a common signaling pathway dependent on protein kinase C and PPAR-γ |
| title_short | Induction of CD36 expression by oxidized LDL and IL-4 by a common signaling pathway dependent on protein kinase C and PPAR-γ |
| title_sort | induction of cd36 expression by oxidized ldl and il 4 by a common signaling pathway dependent on protein kinase c and ppar γ |
| topic | CD36 macrophage scavenger receptor PKC PPAR-g |
| url | http://www.sciencedirect.com/science/article/pii/S0022227520323774 |
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