CD34+ cell-derived CD14+ precursor cells develop into Langerhans cells in a TGF-beta 1-dependent manner

J Immunol. 1999 Nov 1;163(9):4869-77.


Langerhans cells (LC) are CD1a+E-cadherin (E-cad)+Birbeck granule+ but CD11b-CD36-factor XIIIa (FXIIIa)- members of the dendritic cell (DC) family. Evidence holds that LC originate from CD1a+CD14- rather than CD14+CD1a- progenitors, both of which arise from GM-CSF/TNF-alpha-stimulated CD34+ stem cells. The CD14+CD1a- progenitors, on the other hand, can give rise to a separate DC type characterized by its CD1a+CD11b+CD36+FXIIIa+E-cad-BG- phenotype (non-LC DC). Although GM-CSF/TNF-alpha are important for both LC and non-LC DC differentiation, TGF-beta 1 is thought to preferentially promote LC development in vitro and in vivo. However, the hemopoietic biology of this process and the nature of TGF-beta 1-responsive LC precursors (LCp) are not well understood. Here we show that CD14+ precursors in the presence, but not in the absence, of TGF-beta 1 give rise to a progeny that fulfills all major criteria of LC. In contrast, LC development from CD1a+ progenitors was TGF-beta 1 independent. Further studies revealed that CD14+ precursors contain a CD11b+ and a CD11b- subpopulation. When either subset was stimulated with GM-CSF/TNF-alpha and TGF-beta 1, only CD14+CD11b- cells differentiated into LC. The CD11b+ cells, on the other hand, acquired non-LC DC features only. The higher doubling rates of cells entering the CD14+ LCp rather than the CD1a+ LCp pathway add to the importance of TGF-beta 1 for LC development. Because CD14+CD11b- precursors are multipotent cells that can enter LC or macrophage differentiation, it is suggested that these cells, if present at the tissue level, endow a given organ with the property to generate diverse cell types in response to the local cytokine milieu.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antigens, CD1 / biosynthesis
  • Antigens, CD34 / biosynthesis*
  • Antigens, Surface / metabolism
  • Cell Differentiation / immunology
  • Cell Division / immunology
  • Cells, Cultured
  • Cytoplasmic Granules / immunology
  • Cytoplasmic Granules / ultrastructure
  • Dendritic Cells / immunology
  • Dendritic Cells / ultrastructure
  • Fetal Blood / cytology
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / immunology*
  • Hematopoietic Stem Cells / metabolism
  • Hematopoietic Stem Cells / ultrastructure
  • Humans
  • Interphase / immunology
  • Langerhans Cells / cytology*
  • Langerhans Cells / immunology*
  • Langerhans Cells / metabolism
  • Lipopolysaccharide Receptors / biosynthesis*
  • Lymphocyte Activation / immunology
  • Macrophages / cytology
  • T-Lymphocytes / immunology
  • Transforming Growth Factor beta / physiology*


  • Antigens, CD1
  • Antigens, CD34
  • Antigens, Surface
  • Lipopolysaccharide Receptors
  • Transforming Growth Factor beta