Cargando…

Characterization of immune cells in psoriatic adipose tissue

BACKGROUND: Adipose tissue normally contains immune cells that regulate adipocyte function and contribute to metabolic disorders including obesity and diabetes mellitus. Psoriasis is associated with increased risk for metabolic disease, which may in part be due to adipose dysfunction, which has not...

Descripción completa

Detalles Bibliográficos
Autores principales: Rose, Shawn, Stansky, Elena, Dagur, Pradeep K, Samsel, Leigh, Weiner, Elizabeth, Jahanshad, Amir, Doveikis, Julia, Naik, Haley B, Playford, Martin P, McCoy, J Philip, Mehta, Nehal N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197293/
https://www.ncbi.nlm.nih.gov/pubmed/25224267
http://dx.doi.org/10.1186/s12967-014-0258-2
_version_ 1782339597306429440
author Rose, Shawn
Stansky, Elena
Dagur, Pradeep K
Samsel, Leigh
Weiner, Elizabeth
Jahanshad, Amir
Doveikis, Julia
Naik, Haley B
Playford, Martin P
McCoy, J Philip
Mehta, Nehal N
author_facet Rose, Shawn
Stansky, Elena
Dagur, Pradeep K
Samsel, Leigh
Weiner, Elizabeth
Jahanshad, Amir
Doveikis, Julia
Naik, Haley B
Playford, Martin P
McCoy, J Philip
Mehta, Nehal N
author_sort Rose, Shawn
collection PubMed
description BACKGROUND: Adipose tissue normally contains immune cells that regulate adipocyte function and contribute to metabolic disorders including obesity and diabetes mellitus. Psoriasis is associated with increased risk for metabolic disease, which may in part be due to adipose dysfunction, which has not been investigated in psoriasis. There is currently no standardized method for immunophenotyping human adipose tissue. In prior studies, characteristic phenotypic markers of immune cell populations identified in animal models or in other human tissues have been applied in a similar manner to human adipose tissue. Rarely have these populations been verified with confirmatory methodologies or functional studies. Thus, we performed a comprehensive phenotypic and functional analysis of immune cell populations in psoriatic adipose tissue. METHODS: Conventional and imaging flow cytometry were used to define immune cell populations in biopsy specimens of psoriatic adipose tissue (n = 30) including T cells, B cells, NK cells, NKT cells, neutrophils, and macrophages. Relationships between adipose immune cell types and body mass index were determined using Spearman regression analysis, and multivariate linear regression analysis was performed to adjust for cardiometabolic disease risk factors. RESULTS: These analyses revealed a wide range of cell surface receptors on adipose tissue macrophages, which may serve a dual purpose in immunity and metabolism. Further, both CD16+CD56(Lo) and CD16-CD56(Hi) NK cells were found to correlate inversely with body mass index. The relationship between the predominant CD16+CD56(Lo) NK cell population and body mass index persisted after adjusting for age, sex, diabetes, and tobacco use. CONCLUSIONS: Together, these studies enhance our understanding of adipose immune cell phenotype and function, and demonstrate that examination of adipose tissue may provide greater insight into cardiometabolic pathophysiology in psoriasis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12967-014-0258-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4197293
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-41972932014-10-16 Characterization of immune cells in psoriatic adipose tissue Rose, Shawn Stansky, Elena Dagur, Pradeep K Samsel, Leigh Weiner, Elizabeth Jahanshad, Amir Doveikis, Julia Naik, Haley B Playford, Martin P McCoy, J Philip Mehta, Nehal N J Transl Med Research BACKGROUND: Adipose tissue normally contains immune cells that regulate adipocyte function and contribute to metabolic disorders including obesity and diabetes mellitus. Psoriasis is associated with increased risk for metabolic disease, which may in part be due to adipose dysfunction, which has not been investigated in psoriasis. There is currently no standardized method for immunophenotyping human adipose tissue. In prior studies, characteristic phenotypic markers of immune cell populations identified in animal models or in other human tissues have been applied in a similar manner to human adipose tissue. Rarely have these populations been verified with confirmatory methodologies or functional studies. Thus, we performed a comprehensive phenotypic and functional analysis of immune cell populations in psoriatic adipose tissue. METHODS: Conventional and imaging flow cytometry were used to define immune cell populations in biopsy specimens of psoriatic adipose tissue (n = 30) including T cells, B cells, NK cells, NKT cells, neutrophils, and macrophages. Relationships between adipose immune cell types and body mass index were determined using Spearman regression analysis, and multivariate linear regression analysis was performed to adjust for cardiometabolic disease risk factors. RESULTS: These analyses revealed a wide range of cell surface receptors on adipose tissue macrophages, which may serve a dual purpose in immunity and metabolism. Further, both CD16+CD56(Lo) and CD16-CD56(Hi) NK cells were found to correlate inversely with body mass index. The relationship between the predominant CD16+CD56(Lo) NK cell population and body mass index persisted after adjusting for age, sex, diabetes, and tobacco use. CONCLUSIONS: Together, these studies enhance our understanding of adipose immune cell phenotype and function, and demonstrate that examination of adipose tissue may provide greater insight into cardiometabolic pathophysiology in psoriasis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12967-014-0258-2) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-16 /pmc/articles/PMC4197293/ /pubmed/25224267 http://dx.doi.org/10.1186/s12967-014-0258-2 Text en © Rose et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Rose, Shawn
Stansky, Elena
Dagur, Pradeep K
Samsel, Leigh
Weiner, Elizabeth
Jahanshad, Amir
Doveikis, Julia
Naik, Haley B
Playford, Martin P
McCoy, J Philip
Mehta, Nehal N
Characterization of immune cells in psoriatic adipose tissue
title Characterization of immune cells in psoriatic adipose tissue
title_full Characterization of immune cells in psoriatic adipose tissue
title_fullStr Characterization of immune cells in psoriatic adipose tissue
title_full_unstemmed Characterization of immune cells in psoriatic adipose tissue
title_short Characterization of immune cells in psoriatic adipose tissue
title_sort characterization of immune cells in psoriatic adipose tissue
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197293/
https://www.ncbi.nlm.nih.gov/pubmed/25224267
http://dx.doi.org/10.1186/s12967-014-0258-2
work_keys_str_mv AT roseshawn characterizationofimmunecellsinpsoriaticadiposetissue
AT stanskyelena characterizationofimmunecellsinpsoriaticadiposetissue
AT dagurpradeepk characterizationofimmunecellsinpsoriaticadiposetissue
AT samselleigh characterizationofimmunecellsinpsoriaticadiposetissue
AT weinerelizabeth characterizationofimmunecellsinpsoriaticadiposetissue
AT jahanshadamir characterizationofimmunecellsinpsoriaticadiposetissue
AT doveikisjulia characterizationofimmunecellsinpsoriaticadiposetissue
AT naikhaleyb characterizationofimmunecellsinpsoriaticadiposetissue
AT playfordmartinp characterizationofimmunecellsinpsoriaticadiposetissue
AT mccoyjphilip characterizationofimmunecellsinpsoriaticadiposetissue
AT mehtanehaln characterizationofimmunecellsinpsoriaticadiposetissue