Lysophosphatidic acid attenuates the cytotoxic effects and degree of peroxisome proliferator-activated receptor g activation induced by 15-deoxyD(12),(14)-prostaglandin J(2) in neuroblastoma cells
Lysophosphatidic acid attenuates the cytotoxic effects and degree of peroxisome proliferator-activated receptor g activation induced by 15-deoxyD(12),(14)-prostaglandin J(2) in neuroblastoma cells
PPARg (peroxisome proliferator-activated receptor g) is a ligand-activated transcription factor that responds to 15dPGJ(2) (15-deoxy-D(12),(14)-prostglandin J(2)). 15dPGJ(2), in vitro, halts neuroblastoma cell growth, but reported mechanisms vary. Here we evaluated the modulatory effects of endogenous serum lipid mitogens upon the extent of 15dPGJ(2)-induced growth inhibition and on the precise cellular responses of neuroblastoma cells to PPARg activation. We show that 15dPGJ2 specifically inhibited cell growth in both complete and delipidated media. 15dPGJ2-induced growth inhibition was accompanied by decreased cell viability, although the effect was far more marked in delipidated medium than in complete medium. Incubation with 15dPGJ(2) in complete medium resulted in cytoplasmic changes characteristic of type II programmed cell death (autophagy), while prior serum lipid removal resulted in cell death via an apoptotic mechanism. These distinct, serum lipid-dependent cellular responses to 15dPGJ(2) were accompanied by increases in the expression of a reporter gene construct containing a PPAR response element of 2.3-fold in complete medium, but of 4.8-fold in delipidated medium. Restoration of the serum lysolipid LPA (lysophosphaticlic acid) to cells in delipidated medium reduced 15dPGJ(2)-mediated PPARg activation, growth inhibition and cell death; following addition of S1P (sphingosine 1-phosphate), decreases were apparent but more marginal. Further, while the effects of LPA in del ipiclated medium were mediated through a G(i)/phosphomositide 3-kinase/MAPK (mitogen-activated protein kinase) pathway, those of S1P did not involve the MAPK component. These data suggest that the serum lysolipid LPA modulates the degree of PPARg activation and the precise cellular response to 15dPGJ(2) via activation of a G(i)/phosphoinositide 3-kinase/MAPK pathway.
apoptosis, autophagy, lysophosphartidic acid (LPA), neuroblastoma, peroxisome proliferator-activated receptor (PPAR), sphingosine 1-phosphate
83-91
Rodway, Helen A.
977a24c8-7835-46b4-bd4f-c9c5dc890572
Hunt, Alan N.
95a3e223-da96-40e7-b47d-27dce014e305
Kohler, Janice A.
b37f534f-93bc-412e-8631-afb326e0707f
Postle, Anthony D.
0fa17988-b4a0-4cdc-819a-9ae15c5dad66
Lillycrop, Karen A.
eeaaa78d-0c4d-4033-a178-60ce7345a2cc
2 June 2004
Rodway, Helen A.
977a24c8-7835-46b4-bd4f-c9c5dc890572
Hunt, Alan N.
95a3e223-da96-40e7-b47d-27dce014e305
Kohler, Janice A.
b37f534f-93bc-412e-8631-afb326e0707f
Postle, Anthony D.
0fa17988-b4a0-4cdc-819a-9ae15c5dad66
Lillycrop, Karen A.
eeaaa78d-0c4d-4033-a178-60ce7345a2cc
Rodway, Helen A., Hunt, Alan N., Kohler, Janice A., Postle, Anthony D. and Lillycrop, Karen A.
(2004)
Lysophosphatidic acid attenuates the cytotoxic effects and degree of peroxisome proliferator-activated receptor g activation induced by 15-deoxyD(12),(14)-prostaglandin J(2) in neuroblastoma cells.
Biochemical Journal, 382 (1), .
(doi:10.1042/BJ20040107).
Abstract
PPARg (peroxisome proliferator-activated receptor g) is a ligand-activated transcription factor that responds to 15dPGJ(2) (15-deoxy-D(12),(14)-prostglandin J(2)). 15dPGJ(2), in vitro, halts neuroblastoma cell growth, but reported mechanisms vary. Here we evaluated the modulatory effects of endogenous serum lipid mitogens upon the extent of 15dPGJ(2)-induced growth inhibition and on the precise cellular responses of neuroblastoma cells to PPARg activation. We show that 15dPGJ2 specifically inhibited cell growth in both complete and delipidated media. 15dPGJ2-induced growth inhibition was accompanied by decreased cell viability, although the effect was far more marked in delipidated medium than in complete medium. Incubation with 15dPGJ(2) in complete medium resulted in cytoplasmic changes characteristic of type II programmed cell death (autophagy), while prior serum lipid removal resulted in cell death via an apoptotic mechanism. These distinct, serum lipid-dependent cellular responses to 15dPGJ(2) were accompanied by increases in the expression of a reporter gene construct containing a PPAR response element of 2.3-fold in complete medium, but of 4.8-fold in delipidated medium. Restoration of the serum lysolipid LPA (lysophosphaticlic acid) to cells in delipidated medium reduced 15dPGJ(2)-mediated PPARg activation, growth inhibition and cell death; following addition of S1P (sphingosine 1-phosphate), decreases were apparent but more marginal. Further, while the effects of LPA in del ipiclated medium were mediated through a G(i)/phosphomositide 3-kinase/MAPK (mitogen-activated protein kinase) pathway, those of S1P did not involve the MAPK component. These data suggest that the serum lysolipid LPA modulates the degree of PPARg activation and the precise cellular response to 15dPGJ(2) via activation of a G(i)/phosphoinositide 3-kinase/MAPK pathway.
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Submitted date: 20 January 2004
Published date: 2 June 2004
Keywords:
apoptosis, autophagy, lysophosphartidic acid (LPA), neuroblastoma, peroxisome proliferator-activated receptor (PPAR), sphingosine 1-phosphate
Identifiers
Local EPrints ID: 28821
URI: http://eprints.soton.ac.uk/id/eprint/28821
ISSN: 1470-8728
PURE UUID: c154b4f7-c748-49b4-a877-bf8dd2c26d42
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Date deposited: 08 May 2006
Last modified: 16 Mar 2024 02:50
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Author:
Helen A. Rodway
Author:
Alan N. Hunt
Author:
Janice A. Kohler
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