Differentiation Epitopes Define Hematopoietic Stem Cells and Change with Cell Cycle Passage

Stem Cell Rev Rep. 2022 Oct;18(7):2351-2364. doi: 10.1007/s12015-022-10374-4. Epub 2022 May 3.

Abstract

Hematopoietic stem cells express differentiation markers B220 and Gr1 and are proliferative. We have shown that the expression of these entities changes with cell cycle passage. Overall, we conclude that primitive hematopoietic stem cells alter their differentiation potential with cell cycle progression. Murine derived long-term hematopoietic stem cells (LT-HSC) are cycling and thus always changing phenotype. Here we show that over one half of marrow LT-HSC are in the population expressing differentiation epitopes and that B220 and Gr-1 positive populations are replete with LT-HSC after a single FACS separation but if subjected to a second separation these cells no longer contain LT-HSC. However, with second separated cells there is a population appearing that is B220 negative and replete with cycling c-Kit, Sca-1 CD150 positive LT-HSC. There is a 3-4 h interval between the first and second B220 or GR-1 FACS separation during which the stem cells continue to cycle. Thus, the LT-HSC have lost B220 or GR-1 expression as the cells progress through cell cycle, although they have maintained the c-kit, Sca-1 and CD150 stem cells markers over this time interval. These data indicate that cycling stem cells express differentiation epitopes and alter their differentiation potential with cell cycle passage.

Keywords: Cell cycle; Differentiation; Hematopoietic stem cells; Lineage positive cells; Stem cell purification.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Differentiation*
  • Cell Cycle
  • Cell Differentiation / genetics
  • Epitopes
  • Hematopoietic Stem Cells*
  • Mice

Substances

  • Antigens, Differentiation
  • Epitopes