Identification of human NK17/NK1 cells.

BACKGROUND: Natural killer (NK) cells have both cytolytic and immunoregulatory functions. We recently described that these cells release the inflammatory cytokines IL-17 and IFN-γ. However, the precise identity of the NK cell subset(s) that secrete these cytokines is not known. METHODOLOGY/PRINCIPAL...

Full description

Bibliographic Details
Main Authors: Abhilash D Pandya, Zaidoon Al-Jaderi, Rune A Høglund, Trygve Holmøy, Hanne F Harbo, Johannes Norgauer, Azzam A Maghazachi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3198820?pdf=render
id doaj-153c7a7a2c914069b79ec57e9abff285
record_format Article
spelling doaj-153c7a7a2c914069b79ec57e9abff2852020-11-25T00:52:36ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01610e2678010.1371/journal.pone.0026780Identification of human NK17/NK1 cells.Abhilash D PandyaZaidoon Al-JaderiRune A HøglundTrygve HolmøyHanne F HarboJohannes NorgauerAzzam A MaghazachiBACKGROUND: Natural killer (NK) cells have both cytolytic and immunoregulatory functions. We recently described that these cells release the inflammatory cytokines IL-17 and IFN-γ. However, the precise identity of the NK cell subset(s) that secrete these cytokines is not known. METHODOLOGY/PRINCIPAL FINDINGS: To isolate the cells secreting IL-17 and IFN-γ, we took advantage of the findings that Th17/Th1 cells express chemokine receptors. Therefore, CD56(+)NK cells were stained with antibodies against various chemokine receptors and intracellularly with antibodies toward IL-17 and IFN-γ. Consequently, we identified previously unrecognized subset of NK cells generated from normal human peripheral blood after activation with IL-2 but not PMA plus ionomycin. The cells are characterized by the expression of CD56(+) and CCR4(+), produce IL-17 and IFN-γ and are consequently named NK17/NK1 cells. They also express CD161, NKp30, NKp44, NKp46, NKG2D, CD158, CCL22, IL-2Rβ and the common γ chain but not CD127 or IL-23R. Further, they possess T-bet and RORγt transcription factors. Antibodies to IL-1β, IL-6, IL-21, or TGF-β1 do not inhibit IL-2-induced generation of NK17/NK1 cells, suggesting that IL-2 has the capacity to polarize these cells. Notably, NK17/NK1 cells are abundant in the cerebrospinal fluid (CSF) of patients with multiple sclerosis (MS) without activation, and are generated from the peripheral blood of these patients after activation with IL-2. CONCLUSIONS/SIGNIFICANCE: NK17/NK1 cells identified here have not been previously described in healthy or MS patients.http://europepmc.org/articles/PMC3198820?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Abhilash D Pandya
Zaidoon Al-Jaderi
Rune A Høglund
Trygve Holmøy
Hanne F Harbo
Johannes Norgauer
Azzam A Maghazachi
spellingShingle Abhilash D Pandya
Zaidoon Al-Jaderi
Rune A Høglund
Trygve Holmøy
Hanne F Harbo
Johannes Norgauer
Azzam A Maghazachi
Identification of human NK17/NK1 cells.
PLoS ONE
author_facet Abhilash D Pandya
Zaidoon Al-Jaderi
Rune A Høglund
Trygve Holmøy
Hanne F Harbo
Johannes Norgauer
Azzam A Maghazachi
author_sort Abhilash D Pandya
title Identification of human NK17/NK1 cells.
title_short Identification of human NK17/NK1 cells.
title_full Identification of human NK17/NK1 cells.
title_fullStr Identification of human NK17/NK1 cells.
title_full_unstemmed Identification of human NK17/NK1 cells.
title_sort identification of human nk17/nk1 cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description BACKGROUND: Natural killer (NK) cells have both cytolytic and immunoregulatory functions. We recently described that these cells release the inflammatory cytokines IL-17 and IFN-γ. However, the precise identity of the NK cell subset(s) that secrete these cytokines is not known. METHODOLOGY/PRINCIPAL FINDINGS: To isolate the cells secreting IL-17 and IFN-γ, we took advantage of the findings that Th17/Th1 cells express chemokine receptors. Therefore, CD56(+)NK cells were stained with antibodies against various chemokine receptors and intracellularly with antibodies toward IL-17 and IFN-γ. Consequently, we identified previously unrecognized subset of NK cells generated from normal human peripheral blood after activation with IL-2 but not PMA plus ionomycin. The cells are characterized by the expression of CD56(+) and CCR4(+), produce IL-17 and IFN-γ and are consequently named NK17/NK1 cells. They also express CD161, NKp30, NKp44, NKp46, NKG2D, CD158, CCL22, IL-2Rβ and the common γ chain but not CD127 or IL-23R. Further, they possess T-bet and RORγt transcription factors. Antibodies to IL-1β, IL-6, IL-21, or TGF-β1 do not inhibit IL-2-induced generation of NK17/NK1 cells, suggesting that IL-2 has the capacity to polarize these cells. Notably, NK17/NK1 cells are abundant in the cerebrospinal fluid (CSF) of patients with multiple sclerosis (MS) without activation, and are generated from the peripheral blood of these patients after activation with IL-2. CONCLUSIONS/SIGNIFICANCE: NK17/NK1 cells identified here have not been previously described in healthy or MS patients.
url http://europepmc.org/articles/PMC3198820?pdf=render
work_keys_str_mv AT abhilashdpandya identificationofhumannk17nk1cells
AT zaidoonaljaderi identificationofhumannk17nk1cells
AT runeahøglund identificationofhumannk17nk1cells
AT trygveholmøy identificationofhumannk17nk1cells
AT hannefharbo identificationofhumannk17nk1cells
AT johannesnorgauer identificationofhumannk17nk1cells
AT azzamamaghazachi identificationofhumannk17nk1cells
_version_ 1725241325605879808