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Published on: March 28, 2013
Transcriptional coactivator p300 regulates glucose-induced gene expression in endothelial cells
Shali Chen1, Biao Feng, Biju George
1Department of Pathology, University of Western Ontario, Schulich School of Medicine, London, Ontario, Canada.
Abstract:
Sustained hyperglycemia in diabetes causes alteration of a large number of transcription factors and mRNA transcripts, leading to tissue damage. We investigated whether p300, a transcriptional coactivator with histone acetyl transferase activity, regulates glucose-induced activation of transcription factors and subsequent upregulation of vasoactive factors and extracellular matrix (ECM) proteins in human umbilical vein endothelial cells (HUVECs). HUVECs were incubated in varied glucose concentrations and were studied after p300 small interfering RNA (siRNA) transfection, p300 overexpression, or incubation with the p300 inhibitor curcumin. Histone H2AX phosphorylation and lysine acetylation were examined for oxidative DNA damage and p300 activation. Screening for transcription factors was performed with the Luminex system. Alterations of selected transcription factors were validated. mRNA expression of p300, endothelin-1 (ET-1), vascular endothelial growth factor (VEGF), and fibronectin (FN) and its splice variant EDB(+)FN and FN protein production were analyzed. HUVECs in 25 mmol/l glucose showed increased p300 production accompanied by increased binding of p300 to ET-1 and FN promoters, augmented histone acetylation, H2AX phosphorylation, activation of multiple transcription factors, and increased mRNA expression of vasoactive factors and ECM proteins. p300 overexpression showed a glucose-like effect on the mRNA expression of ET-1, VEGF, and FN. Furthermore, siRNA-mediated p300 blockade or chemical inhibitor of p300 prevented such glucose-induced changes. Similar mRNA upregulation was also seen in the organ culture of vascular tissues, which was prevented by p300 siRNA transfection. Data from these studies suggest that glucose-induced p300 upregulation is an important upstream epigenetic mechanism regulating gene expression of vasoactive factors and ECM proteins in endothelial cells and is a potential therapeutic target for diabetic complications.
Insights
High glucose in diabetes activates p300, an epigenetic regulator, leading to increased vasoactive factors and extracellular matrix proteins in endothelial cells, suggesting p300 as a therapeutic target for diabetic complications.
Area of Science:
- Endocrinology and Metabolism
- Molecular Biology
- Epigenetics
Background:
- Sustained hyperglycemia in diabetes mellitus alters transcription factors and mRNA, causing tissue damage.
- Endothelial cells play a critical role in vascular health and are significantly impacted by diabetic conditions.
Purpose of the Study:
- To investigate the role of p300, a transcriptional coactivator, in regulating glucose-induced gene expression in human umbilical vein endothelial cells (HUVECs).
- To determine if p300 acts as an upstream epigenetic mechanism controlling vasoactive factors and extracellular matrix (ECM) proteins in response to hyperglycemia.
Main Methods:
- HUVECs were exposed to varying glucose concentrations and manipulated for p300 levels (siRNA, overexpression) or activity (curcumin inhibitor).
- Assessed histone acetylation, H2AX phosphorylation, and transcription factor activation using Luminex screening and validation.
- Quantified mRNA and protein expression of p300, endothelin-1 (ET-1), vascular endothelial growth factor (VEGF), and fibronectin (FN).
Main Results:
- High glucose (25 mmol/l) increased p300 production, promoter binding, histone acetylation, and transcription factor activation in HUVECs.
- Glucose-induced upregulation of ET-1, VEGF, and FN mRNA was observed, mimicked by p300 overexpression.
- p300 inhibition (siRNA or curcumin) or blockade prevented glucose-induced changes in gene expression in HUVECs and vascular organ cultures.
Conclusions:
- Glucose-induced p300 upregulation is a key upstream epigenetic event in endothelial cells during hyperglycemia.
- p300 regulates the expression of vasoactive factors and ECM proteins, contributing to diabetic complications.
- Targeting p300 presents a potential therapeutic strategy for managing diabetic vascular complications.
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