High-resolution phenotyping identifies NK cell subsets that distinguish healthy children from adults.

Natural killer (NK) cells are critical in immune defense against infected, stressed or transformed cells. Their function is regulated by the heterogeneous expression of a wide array of surface receptors that shape its phenotypic diversity. Although NK cells develop in the bone marrow and secondary l...

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Main Authors: Sanjana Mahapatra, Emily M Mace, Charles G Minard, Lisa R Forbes, Alexander Vargas-Hernandez, Teresa K Duryea, George Makedonas, Pinaki P Banerjee, William T Shearer, Jordan S Orange
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5540415?pdf=render
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author Sanjana Mahapatra
Emily M Mace
Charles G Minard
Lisa R Forbes
Alexander Vargas-Hernandez
Teresa K Duryea
George Makedonas
Pinaki P Banerjee
William T Shearer
Jordan S Orange
author_facet Sanjana Mahapatra
Emily M Mace
Charles G Minard
Lisa R Forbes
Alexander Vargas-Hernandez
Teresa K Duryea
George Makedonas
Pinaki P Banerjee
William T Shearer
Jordan S Orange
author_sort Sanjana Mahapatra
collection DOAJ
description Natural killer (NK) cells are critical in immune defense against infected, stressed or transformed cells. Their function is regulated by the heterogeneous expression of a wide array of surface receptors that shape its phenotypic diversity. Although NK cells develop in the bone marrow and secondary lymphoid tissues, substantive differentiation is apparent in the peripheral blood including known age-related variation. In order to gain greater insight into phenotypic and functional variation within peripheral blood NK cells across age groups, we used multi-parametric, polyfunctional flow cytometry to interrogate the NK cell variability in 20 healthy adults and 15 5-10, 11-15 and 16-20 year-old children. We found that the normative ranges in both adults and children displayed great inter-individual variation for most markers. While the expression of several receptors did not differ, among those that did, the majority of the differences existed between adults and the three pediatric groups, rather than among children of different ages. Interestingly, we also identified variation in the individual expression of some markers by sex and ethnicity. Combinatorial analysis of NK cell receptors revealed intermediate subsets between the CD56bright and CD56dim NK cells. Furthermore, on examining the NK cell diversity by age, adults were discovered to have the lowest developmental diversity. Thus, our findings identify previously unappreciated NK cell subsets potentially distinguishing children from adults and suggest functional correlates that may have relevance in age-specific host defense.
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spelling doaj.art-c93cb059f3524b269ae4a9eb643939e42022-12-21T18:52:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01128e018113410.1371/journal.pone.0181134High-resolution phenotyping identifies NK cell subsets that distinguish healthy children from adults.Sanjana MahapatraEmily M MaceCharles G MinardLisa R ForbesAlexander Vargas-HernandezTeresa K DuryeaGeorge MakedonasPinaki P BanerjeeWilliam T ShearerJordan S OrangeNatural killer (NK) cells are critical in immune defense against infected, stressed or transformed cells. Their function is regulated by the heterogeneous expression of a wide array of surface receptors that shape its phenotypic diversity. Although NK cells develop in the bone marrow and secondary lymphoid tissues, substantive differentiation is apparent in the peripheral blood including known age-related variation. In order to gain greater insight into phenotypic and functional variation within peripheral blood NK cells across age groups, we used multi-parametric, polyfunctional flow cytometry to interrogate the NK cell variability in 20 healthy adults and 15 5-10, 11-15 and 16-20 year-old children. We found that the normative ranges in both adults and children displayed great inter-individual variation for most markers. While the expression of several receptors did not differ, among those that did, the majority of the differences existed between adults and the three pediatric groups, rather than among children of different ages. Interestingly, we also identified variation in the individual expression of some markers by sex and ethnicity. Combinatorial analysis of NK cell receptors revealed intermediate subsets between the CD56bright and CD56dim NK cells. Furthermore, on examining the NK cell diversity by age, adults were discovered to have the lowest developmental diversity. Thus, our findings identify previously unappreciated NK cell subsets potentially distinguishing children from adults and suggest functional correlates that may have relevance in age-specific host defense.http://europepmc.org/articles/PMC5540415?pdf=render
spellingShingle Sanjana Mahapatra
Emily M Mace
Charles G Minard
Lisa R Forbes
Alexander Vargas-Hernandez
Teresa K Duryea
George Makedonas
Pinaki P Banerjee
William T Shearer
Jordan S Orange
High-resolution phenotyping identifies NK cell subsets that distinguish healthy children from adults.
PLoS ONE
title High-resolution phenotyping identifies NK cell subsets that distinguish healthy children from adults.
title_full High-resolution phenotyping identifies NK cell subsets that distinguish healthy children from adults.
title_fullStr High-resolution phenotyping identifies NK cell subsets that distinguish healthy children from adults.
title_full_unstemmed High-resolution phenotyping identifies NK cell subsets that distinguish healthy children from adults.
title_short High-resolution phenotyping identifies NK cell subsets that distinguish healthy children from adults.
title_sort high resolution phenotyping identifies nk cell subsets that distinguish healthy children from adults
url http://europepmc.org/articles/PMC5540415?pdf=render
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