Characterization and functional analysis of novel circulating NK cell sub-populations

Author:

Khummuang Saichit1,Chuensirikulchai Kantinan1,Pata Supansa12,Laopajon Witida12,Chruewkamlow Nuttapol2,Mahasongkram Kodchakorn2,Sugiura Nobuo3,Watanabe Hideto3,Tateno Hiroaki4,Kamuthachad Ludthawun5,Wongratanacheewin Surasakdi5,Takheaw Nuchjira1,Kasinrerk Watchara12ORCID

Affiliation:

1. Division of Clinical Immunology, Department of Medical Technology

2. Biomedical Technology Research Center, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, at the Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, Thailand

3. Institute for Molecular Science of Medicine, Aichi Medical University, Aichi, Japan

4. Biotechnology Research Institute for Drug Discovery, National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki, Japan

5. Department of Microbiology, Faculty of Medicine and Melioidosis Research Center, Khon Kaen University, Khon Kaen, Thailand

Abstract

Abstract Natural killer (NK) cells are innate lymphoid cells having potent cytolytic function that provide host defense against microbial infections and tumors. Using our generated monoclonal antibody (mAb), named FE-1H10, new NK cell sub-populations in peripheral blood were identified. The molecules recognized by mAb FE-1H10 were expressed on a sub-population of CD3−CD56dim NK cells. The epitope recognized by mAb FE-1H10 was demonstrated to be N-glycan and proven to be different from CD57. Upon K562 stimulation, the CD56dimFE-1H10+ NK cell sub-population exhibited significantly lower cytolytic function with low ability to degranulate and release cytolytic granules compared to the CD56dimFE-1H10− NK cell sub-population. Moreover, the CD56dimFE-1H10+ NK cells produced less IFN-γ and TNF-α than the CD56dimFE-1H10− NK cells. We demonstrated here that mAb FE-1H10 could identify two sub-populations of circulating CD56dim NK cells with different functions. Our discovery of new sub-populations of NK cells improves our understanding of NK cell biology and may lead to the development of new approaches for NK cell therapy.

Funder

Thailand Research Fund (TRF) Senior Research Scholar

TRF and the Thailand Office of the Higher Education Commission

Grants-in-Aid for Scientific Research B, KAKENHI

Chiang Mai University

CMU Center of Excellence Project

TRF and Chiang Mai University

Publisher

Oxford University Press (OUP)

Subject

Immunology,General Medicine,Immunology and Allergy

Reference58 articles.

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