Summary
Already in 1973, Benditt and Benditt found that the atherosclerotic plaque was clonal and proposed that it was a neoplasm of vascular smooth muscle cells (VSMC). Recent technical advances have made it possible to analyze somatic mutations in human tissues and show that somatic cells accumulate thousands of mutations during development and aging. While most of the mutations are harmless, some either contribute to disease and aging or are directly disease-causative, as in the formation of tumors in cancer. The arterial wall is in part composed of clonal VSMC elements, making this tissue particularly vulnerable to somatic mutagenesis. However, detailed analysis and insight into the extent of somatic variance in the vascular tissue is lacking. Here we plan to analyze the somatic mutations in the arterial wall and relate it to age-associated cardiovascular disease (CVD). We will create an atlas of somatic mutations in the human arterial wall at single-cell resolution in health and disease. We will apply single-cell sequencing in arterial tissue to map somatic mutations. Functional significance of somatic mutagenesis in the vascular wall will be validated using data on gene regulatory networks of relevance in human CVD and disease models with induced somatic mutations in VSMC. The model will have a mosaic pattern of mutation and fate of mutated cells will be mapped by lineage tracing in the development and progression of CVD. Our research provides insight into the prevalence, nature and functional significance of somatic genetic events in the healthy and diseased vascular wall.
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| Web resources: | https://cordis.europa.eu/project/id/101097871 |
| Start date: | 01-01-2024 |
| End date: | 31-12-2028 |
| Total budget - Public funding: | 2 532 795,00 Euro - 2 532 795,00 Euro |
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Original description
Already in 1973, Benditt and Benditt found that the atherosclerotic plaque was clonal and proposed that it was a neoplasm of vascular smooth muscle cells (VSMC). Recent technical advances have made it possible to analyze somatic mutations in human tissues and show that somatic cells accumulate thousands of mutations during development and aging. While most of the mutations are harmless, some either contribute to disease and aging or are directly disease-causative, as in the formation of tumors in cancer. The arterial wall is in part composed of clonal VSMC elements, making this tissue particularly vulnerable to somatic mutagenesis. However, detailed analysis and insight into the extent of somatic variance in the vascular tissue is lacking. Here we plan to analyze the somatic mutations in the arterial wall and relate it to age-associated cardiovascular disease (CVD). We will create an atlas of somatic mutations in the human arterial wall at single-cell resolution in health and disease. We will apply single-cell sequencing in arterial tissue to map somatic mutations. Functional significance of somatic mutagenesis in the vascular wall will be validated using data on gene regulatory networks of relevance in human CVD and disease models with induced somatic mutations in VSMC. The model will have a mosaic pattern of mutation and fate of mutated cells will be mapped by lineage tracing in the development and progression of CVD. Our research provides insight into the prevalence, nature and functional significance of somatic genetic events in the healthy and diseased vascular wall.Status
SIGNEDCall topic
ERC-2022-ADGUpdate Date
31-07-2023
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