Sp1 and Sp3 transcription factors mediate malondialdehyde-induced collagen alpha 1(I) gene expression in cultured hepatic stellate cells

Malondialdehyde, the end product of lipid peroxidation, has been shown to stimulate collagen alpha1(I) (Col1a1) gene expression. However, mechanisms of this effect are unclear. The purpose of this study was to clarify these mechanisms. Rat hepatic stellate cells were cultured in the presence of 200...

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Bibliographic Details
Published in:The Journal of biological chemistry 2002-08, Vol.277 (34), p.30551-30558
Main Authors: García-Ruiz, Inmaculada, de la Torre, Paz, Díaz, Teresa, Esteban, Elena, Fernández, Inmaculada, Muñoz-Yagüe, Teresa, Solís-Herruzo, José A
Format: Article
Language:English
Subjects:
Animals
Cells, Cultured
Collagen Type I - genetics
DNA-Binding Proteins - physiology
Gene Expression Regulation - drug effects
Liver - cytology
Liver - metabolism
Malondialdehyde - pharmacology
Promoter Regions, Genetic
Rats
Rats, Sprague-Dawley
Sp1 Transcription Factor - physiology
Sp3 Transcription Factor
Transcription Factors - physiology
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Summary:Malondialdehyde, the end product of lipid peroxidation, has been shown to stimulate collagen alpha1(I) (Col1a1) gene expression. However, mechanisms of this effect are unclear. The purpose of this study was to clarify these mechanisms. Rat hepatic stellate cells were cultured in the presence of 200 microm malondialdehyde, and the effects on collagen gene expression and the binding of nuclear proteins to the col1a1 promoter were analyzed. Malondialdehyde treatment induced an increase in the cellular levels of col1a1 mRNA that was abrogated by pretreating cells with cycloheximide, p-hydroxymercuribenzoate, pyridoxal 5'-phosphate, and mithramycin. Transient transfections showed that malondialdehyde exerted its effect through regulatory elements located between -220 and -110 bp of the col1a1 promoter. Gel retardation assays demonstrated that malondialdehyde increased the binding of nuclear proteins to two elements located between -161 and -110 bp of the col1a1 promoter. These bindings were supershifted with Sp1 and Sp3 antibodies. Finally, malondialdehyde increased cellular levels of the Sp1 and Sp3 proteins and Sp1 mRNA. Our data indicated that treatment of hepatic stellate cells with malondialdehyde stimulated col1a1 gene expression by inducing the synthesis of Sp1 and Sp3 and their binding to two regulatory elements located between -161 and -110 bp of the col1a1 promoter.
ISSN:0021-9258
DOI:10.1074/jbc.M203368200