![]() |
|
|
12,14-PGJ2 and 2-Cyclopenten-1-one: Role of the Heat Shock Response
Department of Experimental Pharmacology, University of Naples Federico II, Naples, Italy (A.I., A.I., P.D.M., M.D.R.); Department of Pharmaceutical Sciences, University of Salerno, Fisciano, Italy (P.M.); and Department of Biology, University of Rome Tor Vergata, Rome, Italy (A.Ian., M.G.S.)
The transcription factor heat shock factor 1 (HSF1) plays a key role in the expression of several genes, such as heat shock protein (hsp) genes, which are cytoprotective against several pathological conditions, including inflammation. Cyclopentenone prostaglandins (cyPG) are able to activate HSF1 and induce the synthesis of the 70-kDa hsp (hsp70) in mammalian cells. These molecules are characterized by the presence of a reactive
,
-unsatured carbonyl group in the cyclopentane ring (cyclopentenone) which is the key structure for triggering HSF1 activation. In the present study, we investigated, in carrageenin hind-paw edema, an acute model of inflammation, the effect of double-stranded oligodeoxynucleotides with consensus HSF1 sequence as transcription factor decoys to inhibit HSF1 binding to native DNA sites. We show that HSF1 activation and hsp72 expression occurs in inflamed tissue and that this effect is associated with the remission of the inflammatory reaction. Moreover, we studied the effect of prostaglandin 15-deoxy-
12,14-prostaglandin (PG) J2, of its precursor, PGD2 and, for the first time in vivo, the effect of the cyclopentenone ring structure itself, 2-cyclopenten-1-one. Our results demonstrated that all agents used had anti-inflammatory properties and that this effect was associated with HSF1-induced hsp72 expression in vivo, suggesting that the use of cyclopentenone derivatives may represent a novel therapeutic approach to the treatment of inflammatory diseases.
Address correspondence to: Angela Ianaro, Department of Experimental Pharmacology, University of Naples Federico II, Via D. Montesano 4, 80131, Naples, Italy. E-mail: ianaro{at}unina.it
This article has been cited by other articles:
![]() |
C. Fionda, F. Nappi, M. Piccoli, L. Frati, A. Santoni, and M. Cippitelli Inhibition of Trail Gene Expression by Cyclopentenonic Prostaglandin 15-Deoxy-{Delta}12,14-Prostaglandin J2 in T Lymphocytes Mol. Pharmacol., November 1, 2007; 72(5): 1246 - 1257. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Stamatakis, F. J. Sanchez-Gomez, and D. Perez-Sala Identification of Novel Protein Targets for Modification by 15-Deoxy-{Delta}12,14-Prostaglandin J2 in Mesangial Cells Reveals Multiple Interactions with the Cytoskeleton J. Am. Soc. Nephrol., January 1, 2006; 17(1): 89 - 98. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Nickerson, G. F. Elphick, J. Campisi, B. N. Greenwood, and M. Fleshner Physical activity alters the brain Hsp72 and IL-1{beta} responses to peripheral E. coli challenge Am J Physiol Regulatory Integrative Comp Physiol, December 1, 2005; 289(6): R1665 - R1674. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. S. Musiek, L. Gao, G. L. Milne, W. Han, M. B. Everhart, D. Wang, M. G. Backlund, R. N. DuBois, G. Zanoni, G. Vidari, et al. Cyclopentenone Isoprostanes Inhibit the Inflammatory Response in Macrophages J. Biol. Chem., October 21, 2005; 280(42): 35562 - 35570. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Esposito, A. Iacono, G. M. Raso, M. Pacilio, A. Coppola, R. Di Carlo, and R. Meli Raloxifene, a Selective Estrogen Receptor Modulator, Reduces Carrageenan-Induced Acute Inflammation in Normal and Ovariectomized Rats Endocrinology, August 1, 2005; 146(8): 3301 - 3308. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Ialenti, G. Grassia, P. Di Meglio, P. Maffia, M. Di Rosa, and A. Ianaro Mechanism of the Anti-Inflammatory Effect of Thiazolidinediones: Relationship with the Glucocorticoid Pathway Mol. Pharmacol., May 1, 2005; 67(5): 1620 - 1628. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. J. Sanchez-Gomez, E. Cernuda-Morollon, K. Stamatakis, and D. Perez-Sala Protein Thiol Modification by 15-deoxy-{Delta}12,14-Prostaglandin J2 Addition in Mesangial Cells: Role in the Inhibition of Pro-inflammatory Genes Mol. Pharmacol., November 1, 2004; 66(5): 1349 - 1358. [Abstract] [Full Text] [PDF] |
||||