Human CD62Ldim Neutrophils Identified as a Separate Subset by Proteome Profiling and In Vivo Pulse-Chase Labelling

Tamar Tak, Patrick Wijten, Marjolein Heeres, Peter Pickkers, Arjen Scholten, Albert J.R. Heck, Nienke Vrisekoop, Luke P. Leenen, Jos&eacute A.M. Borghans, Kiki Tesselaar and Leo Koenderman

Key points

  • CD62Ldim neutrophils seen in acute inflammation are of a similar age as segmented neutrophils, banded neutrophils are immature cells

  • CD62Ldim neutrophils cluster separately from banded and normal segmented neutrophils based on proteome profiling


During acute inflammation three neutrophil subsets are found in the blood: neutrophils with a conventional segmented nucleus, neutrophils with a banded nucleus and T-cell-suppressing CD62Ldim neutrophils with a high number of nuclear lobes. In this study ( NCT01766414) we compared the in vivo kinetics and proteomes of banded, mature and hypersegmented neutrophils to determine whether these cell types represent truly different neutrophil subsets or reflect changes induced by LPS activation. Using in vivo pulse-chase labelling of neutrophil DNA with 6,6-2H2-glucose, we found that 2H-labelled banded neutrophils appeared much earlier in blood than labelled CD62Ldim and segmented neutrophils, which shared similar label kinetics. Comparison of the proteomes by cluster analysis revealed that CD62Ldim neutrophils were clearly separate from conventional segmented neutrophils despite having similar kinetics in peripheral blood. Interestingly, the conventional segmented cells are more related at a proteome level to banded cells despite a two days difference in maturation time. The differences between CD62Ldim and mature neutrophils are unlikely to be a direct result of LPS-induced activation, due to the extremely low transcriptional capacity of CD62Ldim neutrophils and the fact that neutrophils do not directly respond to the low dose of LPS used in the study (2ng/kg bodyweight). Therefore, we propose CD62Ldim neutrophils to be a truly separate neutrophil subset that is recruited to the bloodstream in response to acute inflammation.

  • Submitted July 15, 2016.
  • Accepted May 10, 2017.