Identification and Analysis of Natural Killer Cells in Murine Nasal Passages.

Natural killer (NK) cells in the upper respiratory airways are not well characterized. In the current study, we sought to characterize and functionally assess murine nasal NK cells.Using immunohistochemistry and flow cytometry, we compared the nasal NK cells of Ncr1GFP/+ knock-in mice, whose NK cell...

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Main Authors: Kazunari Okada, Shintaro Sato, Ayuko Sato, Ofer Mandelboim, Tatsuya Yamasoba, Hiroshi Kiyono
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4648567?pdf=render
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spelling doaj-afd3447dc324424d9b879d66d5dbac3f2020-11-25T02:29:03ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-011011e014292010.1371/journal.pone.0142920Identification and Analysis of Natural Killer Cells in Murine Nasal Passages.Kazunari OkadaShintaro SatoAyuko SatoOfer MandelboimTatsuya YamasobaHiroshi KiyonoNatural killer (NK) cells in the upper respiratory airways are not well characterized. In the current study, we sought to characterize and functionally assess murine nasal NK cells.Using immunohistochemistry and flow cytometry, we compared the nasal NK cells of Ncr1GFP/+ knock-in mice, whose NK cells produced green fluorescent protein, with their splenic and pulmonary counterparts. In addition, we functionally analyzed the nasal NK cells of these mice in vitro. To assess the in vivo functions of nasal NK cells, C57BL/6 mice depleted of NK cells after treatment with PK136 antibody were nasally infected with influenza virus PR8.Immunohistochemical analysis confirmed the presence of NK cells in the lamina propria of nasal mucosa, and flow cytometry showed that these cells were of NK cell lineage. The expression patterns of Ly49 receptor, CD11b/CD27, CD62L and CD69 revealed that nasal NK cells had an immature and activated phenotype compared with that of their splenic and pulmonary counterparts. Effector functions including degranulation and IFN(interferon)-γ production after in vitro stimulation with phorbol 12-myristate-13-acetate plus ionomycin or IL(interleukin)-12 plus IL-18 were dampened in nasal NK cells, and the depletion of NK cells led to an increased influenza virus titer in nasal passages.The NK cells of the murine nasal passage belong to the conventional NK cell linage and characteristically demonstrate an immature and activated phenotype. Despite their hyporesponsiveness in vitro, nasal NK cells play important roles in the host defense against nasal influenza virus infection.http://europepmc.org/articles/PMC4648567?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Kazunari Okada
Shintaro Sato
Ayuko Sato
Ofer Mandelboim
Tatsuya Yamasoba
Hiroshi Kiyono
spellingShingle Kazunari Okada
Shintaro Sato
Ayuko Sato
Ofer Mandelboim
Tatsuya Yamasoba
Hiroshi Kiyono
Identification and Analysis of Natural Killer Cells in Murine Nasal Passages.
PLoS ONE
author_facet Kazunari Okada
Shintaro Sato
Ayuko Sato
Ofer Mandelboim
Tatsuya Yamasoba
Hiroshi Kiyono
author_sort Kazunari Okada
title Identification and Analysis of Natural Killer Cells in Murine Nasal Passages.
title_short Identification and Analysis of Natural Killer Cells in Murine Nasal Passages.
title_full Identification and Analysis of Natural Killer Cells in Murine Nasal Passages.
title_fullStr Identification and Analysis of Natural Killer Cells in Murine Nasal Passages.
title_full_unstemmed Identification and Analysis of Natural Killer Cells in Murine Nasal Passages.
title_sort identification and analysis of natural killer cells in murine nasal passages.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Natural killer (NK) cells in the upper respiratory airways are not well characterized. In the current study, we sought to characterize and functionally assess murine nasal NK cells.Using immunohistochemistry and flow cytometry, we compared the nasal NK cells of Ncr1GFP/+ knock-in mice, whose NK cells produced green fluorescent protein, with their splenic and pulmonary counterparts. In addition, we functionally analyzed the nasal NK cells of these mice in vitro. To assess the in vivo functions of nasal NK cells, C57BL/6 mice depleted of NK cells after treatment with PK136 antibody were nasally infected with influenza virus PR8.Immunohistochemical analysis confirmed the presence of NK cells in the lamina propria of nasal mucosa, and flow cytometry showed that these cells were of NK cell lineage. The expression patterns of Ly49 receptor, CD11b/CD27, CD62L and CD69 revealed that nasal NK cells had an immature and activated phenotype compared with that of their splenic and pulmonary counterparts. Effector functions including degranulation and IFN(interferon)-γ production after in vitro stimulation with phorbol 12-myristate-13-acetate plus ionomycin or IL(interleukin)-12 plus IL-18 were dampened in nasal NK cells, and the depletion of NK cells led to an increased influenza virus titer in nasal passages.The NK cells of the murine nasal passage belong to the conventional NK cell linage and characteristically demonstrate an immature and activated phenotype. Despite their hyporesponsiveness in vitro, nasal NK cells play important roles in the host defense against nasal influenza virus infection.
url http://europepmc.org/articles/PMC4648567?pdf=render
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