Cellular Barcoding Links B-1a B Cell Potential to a Fetal Hematopoietic Stem Cell State at the Single-Cell Level

Immunity. 2016 Aug 16;45(2):346-57. doi: 10.1016/j.immuni.2016.07.014.

Abstract

Hematopoietic stem cells (HSCs) undergo a functional switch in neonatal mice hallmarked by a decrease in self-renewing divisions and entry into quiescence. Here, we investigated whether the developmental attenuation of B-1a cell output is a consequence of a shift in stem cell state during ontogeny. Using cellular barcoding for in vivo single-cell fate analyses, we found that fetal liver definitive HSCs gave rise to both B-1a and B-2 cells. Whereas B-1a potential diminished in all HSCs with time, B-2 output was maintained. B-1a and B-2 plasticity could be reinitiated in a subset of adult HSCs by ectopic expression of the RNA binding protein LIN28B, a key regulator of fetal hematopoiesis, and this coincided with the clonal reversal to fetal-like elevated self-renewal and repopulation potential. These results anchor the attenuation of B-1a cell output to fetal HSC behavior and demonstrate that the developmental decline in regenerative potential represents a reversible HSC state.

MeSH terms

  • Animals
  • Animals, Newborn
  • B-Lymphocytes / physiology*
  • Cell Differentiation / genetics
  • Cell Plasticity
  • Cell Self Renewal
  • Clone Cells
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Female
  • Hematopoiesis / genetics
  • Hematopoietic Stem Cells / physiology*
  • Immunophenotyping
  • Liver / physiology*
  • Lymphocyte Subsets / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • RNA-Binding Proteins
  • Single-Cell Analysis

Substances

  • DNA-Binding Proteins
  • Lin28b protein, mouse
  • RNA-Binding Proteins