Endovascular biopsy: Strategy for analyzing gene expression profiles of individual endothelial cells obtained from

Zhengda Sun1, Devon A Lawson2, Elizabeth Sinclair3

  • 1Division of Neurointerventional Radiology, Department of Radiology and Biomedical Imaging, University of California, San Francisco, CA, USA.

Insights

Researchers developed a novel endovascular method to collect endothelial cells (ECs) for gene expression analysis. This technique identified distinct EC subpopulations, including those resembling senescent cells, in vascular lesions.

Area of Science:

  • Vascular Biology
  • Molecular Medicine
  • Genomics

Background:

  • Endothelial cells (ECs) play a critical role in vascular health and disease.
  • Understanding EC gene expression is crucial for diagnosing and treating vascular conditions.
  • Current methods for EC collection and analysis can be invasive or yield limited cellular material.

Purpose of the Study:

  • To establish an endovascular strategy for targeted endothelial cell collection.
  • To analyze the gene expression profiles of single endothelial cells obtained via endovascular methods.

Main Methods:

  • Endovascular guide wires were used to collect cells from the intra-iliac artery of patients.
  • Fluorescence-activated cell sorting (FACS) isolated endothelial cells (ECs) from leukocytes.
  • Single-cell quantitative RT-PCR analyzed the expression of 48 genes in collected ECs.

Main Results:

  • 134 ECs and 37 leukocytes were successfully collected and analyzed.
  • Isolated ECs showed higher expression of EC-specific markers compared to leukocytes.
  • Gene expression analysis revealed two distinct EC clusters (A and B), with cluster B exhibiting characteristics of senescent cells.

Conclusions:

  • The combination of endovascular sampling, FACS, and single-cell RT-PCR is a viable approach for EC gene expression profiling.
  • This method allows for the characterization of EC heterogeneity in vascular lesions.
  • The findings suggest the presence of distinct EC subpopulations, including senescent cells, in pathological vascular environments.
Abstract

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