CD1c-Expression by Monocytes - Implications for the Use of Commercial CD1c+ Dendritic Cell Isolation Kits

Martine Schrøder1,2, Guro Reinholt Melum1, Ole J B Landsverk1,2

  • 1Department of Pathology, Oslo University Hospital, Oslo, Norway.

Plos One
|June 17, 2016
PubMed

Insights

Commercial kits designed to isolate CD1c+ dendritic cells (DCs) also isolate monocytes. These two cell types, CD1c+ DCs and CD1c+ monocytes, exhibit distinct immune functions, impacting prior research using these isolation kits.

Area of Science:

  • Immunology
  • Cell Biology

Background:

  • Conventional dendritic cells (cDCs) are key regulators of immune responses.
  • CD1c+ cDCs are known for their ability to activate naive CD4+ T cells.
  • CD1c is widely used to identify human CD1c+ cDCs in blood and tissues.

Purpose of the Study:

  • To investigate the specificity of CD1c as a marker for human dendritic cells.
  • To determine if other immune cells express CD1c.
  • To evaluate the functional differences between CD1c+ cDCs and other CD1c-expressing cells.

Main Methods:

  • Flow cytometry analysis of human blood samples.
  • Isolation of cell populations using a commercial CD1c (BDCA-1)+ Dendritic Cell Isolation Kit.
  • Comparative analysis of surface marker expression, cytokine production, and T cell activation capabilities.

Main Results:

  • Both conventional dendritic cells (cDCs) and classical/intermediate monocytes express CD1c.
  • The commercial CD1c (BDCA-1)+ Dendritic Cell Isolation Kit isolates two distinct populations: CD1c+CD14- cDCs and CD1c+CD14+ monocytes.
  • CD1c+ cDCs and CD1c+ monocytes display significantly different surface marker expression, cytokine profiles, and T cell stimulatory capacities.

Conclusions:

  • CD1c is not exclusively expressed on human cDCs; monocytes also express this marker.
  • The commercial CD1c (BDCA-1)+ Dendritic Cell Isolation Kit isolates a mixed population of cDCs and monocytes.
  • Previous studies using this kit to characterize CD1c+ cDCs may need re-evaluation due to the co-isolation of monocytes.

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