Results of an international survey about methods used to isolate human endothelial colony-forming cells: guidance from the SSC on Vascular Biology of the ISTH

J Thromb Haemost. 2023 Sep;21(9):2611-2619. doi: 10.1016/j.jtha.2023.06.014. Epub 2023 Jun 17.

Abstract

Background: Assessment of endothelial colony-forming cell (ECFC) number and vasculogenic properties is crucial for exploring vascular diseases and regeneration strategies. A previous survey of the Scientific and Standardization Committee on Vascular Biology of the International Society on Thrombosis and Haemostasis clarified key methodological points but highlighted a lack of standardization associated with ECFC culture.

Objectives: The aim of this study was to provide expert consensus guidance on ECFC isolation and culture.

Methods: We surveyed 21 experts from 10 different countries using a questionnaire proposed during the 2019 International Society on Thrombosis and Haemostasis Congress in Melbourne (Australia) to attain a consensus on ECFC isolation and culture.

Results: We report here the consolidated results of the questionnaire. There was agreement on several general statements, mainly the technical aspects of ECFC isolation and cell culture. In contrast, on the points concerning the definition of a colony of ECFCs, the quantification of ECFCs, and the estimation of their age (in days or number of passages), the expert opinions were widely dispersed.

Conclusion: Our survey clearly indicates an unmet need for rigorous standardization, multicenter comparison of results, and validation of ECFC isolation and culture procedures for clinical laboratory practice and robustness of results. To this end, we propose a standardized protocol for the isolation and expansion of ECFCs from umbilical cord and adult peripheral blood.

Keywords: ECFC; ISTH; endothelial colony-forming cells; endothelial progenitor cells; standardization; survey.

Publication types

  • Multicenter Study

MeSH terms

  • Adult
  • Australia
  • Biology
  • Cell Culture Techniques*
  • Cells, Cultured
  • Endothelial Cells*
  • Humans
  • Neovascularization, Physiologic