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Singlecell Rna Sequencing Reveals Sex Differences In The Subcellular Composition And Associated Generegulatory Network Activity Of Human Carotid Plaques Katyayanisukhavasigmailcom Johanbjorkegrenkise

  • SKU: BELL-234425368
Singlecell Rna Sequencing Reveals Sex Differences In The Subcellular Composition And Associated Generegulatory Network Activity Of Human Carotid Plaques Katyayanisukhavasigmailcom Johanbjorkegrenkise
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Singlecell Rna Sequencing Reveals Sex Differences In The Subcellular Composition And Associated Generegulatory Network Activity Of Human Carotid Plaques Katyayanisukhavasigmailcom Johanbjorkegrenkise instant download after payment.

Publisher: the Authors
File Extension: PDF
File size: 16.93 MB
ISBN: 101038/S4416102500628Y
Language: English
Year: 2025

Product desciption

Singlecell Rna Sequencing Reveals Sex Differences In The Subcellular Composition And Associated Generegulatory Network Activity Of Human Carotid Plaques Katyayanisukhavasigmailcom Johanbjorkegrenkise by [email protected]; [email protected] 101038/S4416102500628Y instant download after payment.

Nature Cardiovascular Research, doi:10.1038/s44161-025-00628-y

Carotid stenosis causes ischemic stroke in both sexes, but the clinical presentation and plaque characteristics difer. Here we run deep single-cell Check for updatessequencing of 7,690 human carotid plaque cells from male and female patients. While we found no sex diferences in major cell types, we identifed a predominance of the osteogenic phenotype in smooth muscle cells, immunomodulating macrophages (MPs) and endothelial cells (ECs) undergoing endothelial-to-mesenchymal transition in females. In males, we found smooth muscle cells with the chondrocytic phenotype, MPs involved in tissue remodeling and ECs with angiogenic activity. Sex-biased subcellular clusters were integrated with tissue-specifc gene-regulatory networks (GRNs) from the Stockholm–Tartu Atherosclerosis Reverse Network Engineering Task study. We identifed GRN195 involved in angiogenesis and T cell-mediated cytotoxicity in male ECs, while in females, we found GRN33 and GRN122 related to TREM2−/TREM1+ MPs and endothelial-to-mesenchymal transition. The impact of GRN195 on EC proliferation in males was functionally validated, providing evidence for potential therapy targets for atherosclerosis that are sex specifc.

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