1. DNA methylation regulates lineage-specifying genes in primary lymphatic and blood endothelial cells
- Author
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Simone Brönneke, Nils Peters, Bodo Brückner, Sabine Hagemann, Horst Wenck, Marc Winnefeld, Thomas C. G. Bosch, and Franz Stäb
- Subjects
Adult ,Cancer Research ,Physiology ,Angiogenesis ,Cellular differentiation ,government.form_of_government ,Clinical Biochemistry ,Biology ,Epigenesis, Genetic ,Humans ,Epigenetics ,Aged ,Gene Expression Profiling ,Transdifferentiation ,Endothelial Cells ,DNA Methylation ,Middle Aged ,Cell biology ,Gene expression profiling ,Lymphatic Endothelium ,Lymphatic system ,Gene Expression Regulation ,Organ Specificity ,DNA methylation ,government ,Female - Abstract
During embryonic development, the lymphatic system emerges by transdifferentiation from the cardinal vein. Although lymphatic and blood vasculature share a close molecular and developmental relationship, they display distinct features and functions. However, even after terminal differentiation, transitions between blood endothelial cells (BEC) and lymphatic endothelial cells (LEC) have been reported. Since phenotypic plasticity and cellular differentiation processes frequently involve epigenetic mechanisms, we hypothesized that DNA methylation might play a role in regulating cell type-specific expression in endothelial cells. By analyzing global gene expression and methylation patterns of primary human dermal LEC and BEC, we identified a highly significant set of genes, which were differentially methylated and expressed. Pathway analyses of the differentially methylated and upregulated genes in LEC revealed involvement in developmental and transdifferentiation processes. We further identified a set of novel genes, which might be implicated in regulating BEC-LEC plasticity and could serve as therapeutic targets and/or biomarkers in vascular diseases associated with alterations in the endothelial phenotype.
- Published
- 2011