J Leukoc Biol, 2020

CD56dimCD57−NKG2C+ NK cells retaining proliferative potential are possible precursors of CD57+NKG2C+ memory‐like NK cells

This includes a decrease in the expression level of the adapter chain FcεRIγ, NKp30, and NKG2A receptors and an increase in the expression of NKG2C receptor, some KIR family receptors, and co-stimulating molecule CD2. Besides, adaptive-like NK cells are characterized by surface expression of CD57, a marker of highly differentiated cells. Here, it is shown that CD57-negative CD56dimNKG2C+ NK cells may undergo the same changes, as established by the similarity of the phenotypic expression pattern with that of the adaptive-like CD57+NKG2C+ NK cells. Regardless of their differentiation stage, NKG2C-positive NK cells had increased HLA-DR expression indicating an activated state, both ex vivo and after cultivation in stimulating conditions. Additionally, CD57−NKG2C+ NK cells exhibited better proliferative activity compared to CD57+NKG2C+ and NKG2C− NK cells, while retaining high level of natural cytotoxicity. Thus, CD57−NKG2C+ NK cells may represent a less differentiated, but readily expanding stage of the adaptive-like CD57+NKG2C+ NK cells. Moreover, it is shown that NK cells have certain phenotypic plasticity and may both lose NKG2C expression and acquire it de novo during proliferation, induced by IL-2 and K562-mbIL21 feeder cells.

IBCH: 8787
Ссылка на статью в журнале: https://doi.org/10.1002/JLB.1MA0720-654RR
Нет данных о цитировании
Данные статьи проверены модераторами 2020-10-05

Список научных проектов, где отмечена публикация

  1. - (January 6, 2019 — December 31, 2021). Kovalenko E.I.. Grant, RSF.