Volume 98, Issue 4 p. 368-374
ORIGINAL ARTICLE

Expression and function of DNAM‐1 on human B‐lineage cells

Yuko Nagayama‐Hasegawa

Department of Immunology, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan

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Shin‐ichiro Honda

Department of Immunology, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan

Life Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA), University of Tsukuba, Tsukuba, Ibaraki, Japan

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Akira Shibuya

Department of Immunology, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan

Life Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA), University of Tsukuba, Tsukuba, Ibaraki, Japan

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Kazuko Shibuya

Corresponding Author

Department of Immunology, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan

Correspondence

Kazuko Shibuya, Department of Immunology, Faculty of Medicine, University of Tsukuba, 1‐1‐1, Ten‐nodai, Tsukuba, Ibaraki 305‐8575, Japan.

Email: kazukos@md.tsukuba.ac.jp

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First published: 29 November 2019
Citations: 1
The authors declare no conflict of interest.

Funding information: Japan Society for the Promotion of Science, Grant/Award Numbers: 15H01365, 16H05169, 16H06387; Ministry of Education

Abstract

Background

Although DNAM‐1 is an activating receptor constitutively expressed on the majority of NK cells, CD8+ T cells, CD4+ T cells, monocytes, and platelets in human, several evidences demonstrated that a small population in B‐lineage cells also expressed DNAM‐1. However, the expression profile of DNAM‐1 on B‐lineage cells and its function remain obscure. Previous reports revealed that a considerable number of leukocytes including B cells in the peripheral blood conjugated to platelet. Thus, the proportion of DNAM‐1+ B‐lineage cells determined by flow cytometry analysis in the previous reports might be overestimated.

Methods

We examined whether platelets conjugate B cells and then analyzed the expression of DNAM‐1 on the subpopulations of B‐lineage cells according to their maturation stages after exclusion of platelet‐conjugated B cells. We also assessed the involvement of DNAM‐1 in IL‐10 and antibody production from cultured B‐lineage cells stimulated with CpG‐ODN.

Results

Approximately 10% of human DNAM‐1+ CD19+ B cells in the peripheral blood conjugated to platelets, resulting in the overestimation of the proportion of DNAM‐1+ B cells. After exclusion of platelet‐conjugating B cells, we show that DNAM‐1 expression was detected on subpopulations of memory B cells, plasmablasts, and plasma cells and upregulated by stimulation with CpG‐ODN. Moreover, DNAM‐1 was involved in IL‐10 and antibody productions by B cells after CpG‐ODN stimulation.

Conclusions

DNAM‐1 may be involved in B‐lineage cell‐mediated immune responses.

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