Polyclonal regeneration of mouse bone marrow endothelial cells after irradiative conditioning

Cell Rep. 2024 Nov 26;43(11):114779. doi: 10.1016/j.celrep.2024.114779. Epub 2024 Oct 26.

Abstract

Bone marrow endothelial cells (BM-ECs) are the essential components of the BM niche and support the function of hematopoietic stem cells (HSCs). However, conditioning for HSC transplantation causes damage to the recipients' BM-ECs and may lead to transplantation-related morbidity. Here, we investigated the cellular and clonal mechanisms of BM-EC regeneration after irradiative conditioning. Using single-cell RNA sequencing, imaging, and flow cytometry, we revealed how the heterogeneous pool of BM-ECs changes during regeneration from irradiation stress. Next, we developed a single-cell in vitro clonogenic assay and demonstrated that all EC fractions hold a high potential to reenter the cell cycle and form vessel-like structures. Finally, we used Rainbow mice and a machine-learning-based model to show that the regeneration of BM-ECs after irradiation is mostly polyclonal and driven by the broad fraction of BM-ECs; however, the cell output among clones varies at later stages of regeneration.

Keywords: CP: Stem cell research; bone marrow endothelial cells; bone marrow niche; bone marrow regeneration; conditioning; hematopoietic stem cells; irradiation; sinusoids; transplantation.

MeSH terms

  • Animals
  • Bone Marrow Cells* / cytology
  • Endothelial Cells* / radiation effects
  • Hematopoietic Stem Cell Transplantation / methods
  • Hematopoietic Stem Cells / metabolism
  • Hematopoietic Stem Cells / radiation effects
  • Mice
  • Mice, Inbred C57BL
  • Regeneration* / radiation effects