Impact of the -1T>C single-nucleotide polymorphism of the CD40 gene on the development of endothelial dysfunction in a pro-diabetic microenvironment
BACKGROUND AND AIMS: Hyperglycemia reinforces pro-inflammatory conditions that enhance CD40 expression in endothelial cells (EC). Thymine to cytosine transition (-1T > C) in the promoter of the CD40 gene (rs1883832) further increases the abundance of CD40 protein on the EC surface. This study exa...
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| Hauptverfasser: | , , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2024
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| In: |
Atherosclerosis
Year: 2024, Jahrgang: 394, Pages: 1-13 |
| ISSN: | 1879-1484 |
| DOI: | 10.1016/j.atherosclerosis.2023.117386 |
| Online-Zugang: | Verlag, kostenfrei, Volltext: https://doi.org/10.1016/j.atherosclerosis.2023.117386
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| Verfasserangaben: | Pooja Joshi, Franziska Mohr, Cordula Rumig, Elisabeth Kliemank, Guido Krenning, Stefan Kopf, Markus Hecker, Andreas H. Wagner |
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| 245 | 1 | 0 | |a Impact of the -1T>C single-nucleotide polymorphism of the CD40 gene on the development of endothelial dysfunction in a pro-diabetic microenvironment |c Pooja Joshi, Franziska Mohr, Cordula Rumig, Elisabeth Kliemank, Guido Krenning, Stefan Kopf, Markus Hecker, Andreas H. Wagner |
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| 520 | |a BACKGROUND AND AIMS: Hyperglycemia reinforces pro-inflammatory conditions that enhance CD40 expression in endothelial cells (EC). Thymine to cytosine transition (-1T > C) in the promoter of the CD40 gene (rs1883832) further increases the abundance of CD40 protein on the EC surface. This study examines potential associations of the -1T > C SNP of the CD40 gene with type 1 (T1D) or type 2 (T2D) diabetes. Moreover, it investigates the impact of a pro-inflammatory diabetic microenvironment on gene expression in human cultured umbilical vein EC (HUVEC) derived from CC- vs. TT-genotype donors. - METHODS: Tetra-ARMS-PCR was used to compare genotype distribution in 252 patients with diabetes. Soluble CD40 ligand (sCD40L) and soluble CD40 receptor (sCD40) plasma levels were monitored using ELISA. RNA-sequencing was performed with sCD40L-stimulated CC- and TT-genotype HUVEC. Quantitative PCR, Western blot, multiplex-sandwich ELISA array, and immunocytochemistry were used to analyse changes in gene expression in these cells. - RESULTS: Homozygosity for the C-allele was associated with a significant 4.3-fold higher odds of developing T2D as compared to individuals homozygous for the T-allele. Inflammation and endothelial-to-mesenchymal transition (EndMT) driving genes were upregulated in CC-genotype but downregulated in TT-genotype HUVEC when exposed to sCD40L. Expression of EndMT markers significantly increased while that of endothelial markers decreased in HUVEC following exposure to hyperglycemia, tumour necrosis factor-α and sCD40L. - CONCLUSIONS: The -1T > C SNP of the CD40 gene is a risk factor for T2D. Depending on the genotype, it differentially affects gene expression in human cultured EC. CC-genotype HUVEC adopt a pro-inflammatory and intermediate EndMT-like phenotype in a pro-diabetic microenvironment. | ||
| 650 | 4 | |a Adult | |
| 650 | 4 | |a Aged | |
| 650 | 4 | |a CD40 | |
| 650 | 4 | |a CD40 Antigens | |
| 650 | 4 | |a CD40 Ligand | |
| 650 | 4 | |a Cells, Cultured | |
| 650 | 4 | |a Cellular Microenvironment | |
| 650 | 4 | |a Diabetes Mellitus, Type 1 | |
| 650 | 4 | |a Diabetes Mellitus, Type 2 | |
| 650 | 4 | |a Endothelial cells | |
| 650 | 4 | |a Endothelial-to-mesenchymal transition | |
| 650 | 4 | |a Female | |
| 650 | 4 | |a Genetic Predisposition to Disease | |
| 650 | 4 | |a Homozygote | |
| 650 | 4 | |a Human Umbilical Vein Endothelial Cells | |
| 650 | 4 | |a Humans | |
| 650 | 4 | |a Male | |
| 650 | 4 | |a Middle Aged | |
| 650 | 4 | |a Phenotype | |
| 650 | 4 | |a Polymorphism, Single Nucleotide | |
| 650 | 4 | |a Promoter Regions, Genetic | |
| 650 | 4 | |a Risk Factors | |
| 650 | 4 | |a Single nucleotide polymorphism | |
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