Identification of a unique 'switch' for blood vessel generation
Although comprehensive epigenetic datasets, especially in cancer cells or stem (ES/iPS) cells, have been constructed, the changes in epigenome dynamics in normal vascular endothelial cells upon angiogenesis stimulation are still not completely understood. New research from Dr. Minami is expected to lead to the compilation of an epigenomic database for normal endothelial cells and selective epigenomic drug discovery to protect against age-related vascular diseases.
The vascular network that extends throughout the body is the foundation of the biological homeostasis that keeps the body in a steady state. Endothelial cells form the basis of these blood vessels, and their proper functioning is necessary for human health. If the vascular system is over-activated or activated at misplaced regions, it may lead to cancer, heart disease, or cerebrovascular disease. However, revealing the detailed mechanisms of endothelial cell activation-mediated postnatal angiogenesis and epigenomic changes has proven to be challenging research.
To tackle this problem, Dr. Minami and his team conducted a genome-wide analysis of epigenetic changes (mRNAs and histone modification changes) in VEGF (vascular endothelial growth factor essential for angiogenesis) signaling over a minute-by-minute basis. They then cataloged and mapped the changes to understand where changes occurred. In addition, they used a mouse model to evaluate whether the histone-mark changes from their comprehensive database are critical for postnatal angiogenesis.
They found that when vascular endothelial cells receive VEGF signaling, a unique “bivalent histone switch” that is limited to immediate-early type transcription factors essential for angiogenesis is triggered, coinciding with the timing of the transfer of the transcription factor NFAT (which is involved in, among other things, the immune response and cardiac muscle development) into the nucleus.
The term “bivalent” refers to the fact that H3K27me3 (a transcriptional brake) and H3K4me3 (a transcriptional accelerator), which mark epigenetic histone modifications, coexist in the region where transcription factors are expressed. The two marks (H3K27me3 and H3K4me3) are known to occur in the regulatory region of transcription factor expression during the differentiation of stem (ES/iPS) cells. However, the bivalent switch in endothelial cells is highly dynamic and specific, occurring in the gene region of a group of angiogenesis-inducing/-essential transcription factors fully enriched in H3K27me3 brake marks. The non-canonical PRC1 is considered to be functionally different from the canonical PRC1. In the endothelium, non-canonical PRC1.3 binds to this genomic region 15 minutes after VEGF stimulation and disables brakes until the canonical PRC1-brake returns to the endothelium at 60 minutes. After 15 minutes of VEGF treatment, and at the same time as NFAT nuclear localization, NFAT interacts with PTIP-triggered H3K4me3 markers at the region of immediate-early type transcription factors, resulting in an angiogenesis-specific bivalent switch. PTIP is a component (guidance factor) of the MLL3/4, H3K4me3 marking enzyme.
The researchers also found endothelial cell-specific removal of PRC1.3 and PTIP suppressed only postnatal VEGF-induced angiogenesis without affecting developmental blood vessels, thereby delaying cancer growth and suppressing pathological inflammation.
Recently, the epigenome has come to be regarded as “chromatin biology” and includes histone modifications and nuclear structures. It has been mainly studied in ES/iPS cells and cancer cells. This is the first time an epigenetic database of normal endothelial cells has been established. The researchers expect that it will lay the foundation for endothelial activation analyses, which will lead to the future of angiogenesis research.
Dr. Minami commented that, “We believe that the development of drugs that specifically inhibit PTIP-NFAT interaction, as well as epigenomic drugs focused on non-canonical PRC1.3, are expected to lead the way to selective drug discovery that will protect against the vascular diseases found in aging.”