Lymphoid priming in human bone marrow begins before expression of CD10 with upregulation of L-selectin

Nat Immunol. 2012 Oct;13(10):963-71. doi: 10.1038/ni.2405. Epub 2012 Sep 2.

Abstract

Expression of the cell-surface antigen CD10 has long been used to define the lymphoid commitment of human cells. Here we report a unique lymphoid-primed population in human bone marrow that was generated from hematopoietic stem cells (HSCs) before onset of the expression of CD10 and commitment to the B cell lineage. We identified this subset by high expression of the homing molecule L-selectin (CD62L). CD10(-)CD62L(hi) progenitors had full lymphoid and monocytic potential but lacked erythroid potential. Gene-expression profiling placed the CD10(-)CD62L(hi) population at an intermediate stage of differentiation between HSCs and lineage-negative (Lin(-)) CD34(+)CD10(+) progenitors. CD62L was expressed on immature thymocytes, and its ligands were expressed at the cortico-medullary junction of the thymus, which suggested a possible role for this molecule in homing to the thymus. Our studies identify the earliest stage of lymphoid priming in human bone marrow.

Publication types

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

MeSH terms

  • Antigens, CD34 / immunology
  • Antigens, CD34 / metabolism
  • Antigens, CD7 / immunology
  • Bone Marrow Cells / immunology*
  • Bone Marrow Cells / metabolism
  • Cell Differentiation
  • Cell Lineage
  • Cells, Cultured
  • Gene Expression Profiling
  • Hematopoietic Stem Cells / immunology
  • Hematopoietic Stem Cells / metabolism*
  • Humans
  • L-Selectin / biosynthesis*
  • Neprilysin / biosynthesis*
  • Thymocytes / immunology
  • Thymocytes / metabolism
  • Thymus Gland / metabolism
  • Up-Regulation

Substances

  • Antigens, CD34
  • Antigens, CD7
  • L-Selectin
  • Neprilysin