Cyclopentanone prostaglandins induce endothelial cell apoptosis independent of peroxisome proliferator activated receptor-γ
Author(s)
Erl, W
Weber, C
Zernecke, A
Neuzil, J
Vosseler, CA
Kim, HJ
Weber, PC
Griffith University Author(s)
Year published
2004
Metadata
Show full item recordAbstract
Cyclopentenone prostaglandins (CP-PG), such as prostaglandin A1 (PGA1) or 15-deoxy-12,14-prostaglandin J2 (PGJ2), induce apoptosis in different cell types. PGJ2 is also a potent activator of the peroxisome proliferator-activated receptor- (PPAR). We investigated whether PPAR regulates CP-PG-induced apoptosis in endothelial cells (EC). We show that CP-PG induce apoptosis in human umbilical vein EC (HUVEC). Incubation with PGA1 or PGJ2 for 24 h reduced HUVEC number and viability, while the synthetic activators Wy14643 or rosiglitazone had no effect. Flow cytometry and cell cycle analysis revealed externalized phosphatidylserine, ...
View more >Cyclopentenone prostaglandins (CP-PG), such as prostaglandin A1 (PGA1) or 15-deoxy-12,14-prostaglandin J2 (PGJ2), induce apoptosis in different cell types. PGJ2 is also a potent activator of the peroxisome proliferator-activated receptor- (PPAR). We investigated whether PPAR regulates CP-PG-induced apoptosis in endothelial cells (EC). We show that CP-PG induce apoptosis in human umbilical vein EC (HUVEC). Incubation with PGA1 or PGJ2 for 24 h reduced HUVEC number and viability, while the synthetic activators Wy14643 or rosiglitazone had no effect. Flow cytometry and cell cycle analysis revealed externalized phosphatidylserine, caspase-3 activation, and an increased percentage of cellswith a reduced DNA content by CP-PG treatment. EMSA demonstrated an activation of PPAR by PGJ2 and rosiglitazone. Immunohistochemistry of HUVEC and immunoblot analyses of protein extracts showed that PPAR was localized in the nuclei of HUVEC, and that CP-PG treatment decreased the amount of PPAR protein. This degradation was prevented by a pan-caspase inhibitor. Treatment of differentiated, endothelial-like PPAR-deficient stem cells, or of HUVEC transfected with dominant-negative PPAR with CP-PG, induced cell death and apoptosis. Our findings show that PGA1 and PGJ2 induce apoptosis in endothelial cells independent of PPAR. As the synthesis of PGJ2 is increased at sites of inflammation, our results may suggest a possiblemechanism for endothelial damage.
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View more >Cyclopentenone prostaglandins (CP-PG), such as prostaglandin A1 (PGA1) or 15-deoxy-12,14-prostaglandin J2 (PGJ2), induce apoptosis in different cell types. PGJ2 is also a potent activator of the peroxisome proliferator-activated receptor- (PPAR). We investigated whether PPAR regulates CP-PG-induced apoptosis in endothelial cells (EC). We show that CP-PG induce apoptosis in human umbilical vein EC (HUVEC). Incubation with PGA1 or PGJ2 for 24 h reduced HUVEC number and viability, while the synthetic activators Wy14643 or rosiglitazone had no effect. Flow cytometry and cell cycle analysis revealed externalized phosphatidylserine, caspase-3 activation, and an increased percentage of cellswith a reduced DNA content by CP-PG treatment. EMSA demonstrated an activation of PPAR by PGJ2 and rosiglitazone. Immunohistochemistry of HUVEC and immunoblot analyses of protein extracts showed that PPAR was localized in the nuclei of HUVEC, and that CP-PG treatment decreased the amount of PPAR protein. This degradation was prevented by a pan-caspase inhibitor. Treatment of differentiated, endothelial-like PPAR-deficient stem cells, or of HUVEC transfected with dominant-negative PPAR with CP-PG, induced cell death and apoptosis. Our findings show that PGA1 and PGJ2 induce apoptosis in endothelial cells independent of PPAR. As the synthesis of PGJ2 is increased at sites of inflammation, our results may suggest a possiblemechanism for endothelial damage.
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Journal Title
European Journal of Immunology
Volume
34
Copyright Statement
© 2004 John Wiley & Sons, Ltd. Self-archiving of the author-manuscript version is not yet supported by this publisher. Please refer to the journal link for access to the definitive, published version or contact the author for more information.
Subject
Immunology