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Neutrophils are immune cells preferentially targeted by retinoic acid in elderly subjects

BACKGROUND: The immune system gradually deteriorates with age and nutritional status is a major factor in immunosenescence. Of the many nutritional factors implicated in age-related immune dysfunction, vitamin A may be a good candidate, since vitamin A concentrations classically decrease during agin...

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Autores principales: Minet-Quinard, Régine, Farges, M Chantal, Thivat, Emilie, Deleine, Cécile, Mayot, Gilles, Brtko, Julius, Ribalta, Josep, Winklhofer-Roob, Brigitte, Rock, Edmond, Vasson, M Paule
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940875/
https://www.ncbi.nlm.nih.gov/pubmed/20727130
http://dx.doi.org/10.1186/1742-4933-7-10
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author Minet-Quinard, Régine
Farges, M Chantal
Thivat, Emilie
Deleine, Cécile
Mayot, Gilles
Brtko, Julius
Ribalta, Josep
Winklhofer-Roob, Brigitte
Rock, Edmond
Vasson, M Paule
author_facet Minet-Quinard, Régine
Farges, M Chantal
Thivat, Emilie
Deleine, Cécile
Mayot, Gilles
Brtko, Julius
Ribalta, Josep
Winklhofer-Roob, Brigitte
Rock, Edmond
Vasson, M Paule
author_sort Minet-Quinard, Régine
collection PubMed
description BACKGROUND: The immune system gradually deteriorates with age and nutritional status is a major factor in immunosenescence. Of the many nutritional factors implicated in age-related immune dysfunction, vitamin A may be a good candidate, since vitamin A concentrations classically decrease during aging whereas it may possess important immunomodulatory properties via its active metabolites, the retinoic acids. This prompted us to investigate the immune response induced by retinoids in adults and elderly healthy subjects. Before and after oral supplementation with 13cis retinoic acid (0.5 mg/kg/day during 28 days), whole blood cells were phenotyped, and functions of peripheral blood mononuclear cells (PBMC) and polymorphonuclear cells (PMN) were investigated by flow cytometry and ELISA tests. RESULTS: In both young adults (n = 20, 25 ± 4 years) and older subjects (n = 20, 65 ± 4 years), retinoic acid supplementation had no effect on the distribution of leukocyte subpopulations or on the functions of PBMC (Il-2 and sIl-2R production, membrane expression of CD25). Concerning PMN, retinoic acid induced an increase in both spontaneous migration and cell surface expression of CD11b in the two different age populations, whereas bactericidal activity and phagocytosis remained unchanged. CONCLUSIONS: We demonstrated that retinoic acid induces the same intensity of immune response between adult and older subjects, and more specifically affects PMN functions, i.e. adhesion and migration, than PBMC functions.
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spelling pubmed-29408752010-09-17 Neutrophils are immune cells preferentially targeted by retinoic acid in elderly subjects Minet-Quinard, Régine Farges, M Chantal Thivat, Emilie Deleine, Cécile Mayot, Gilles Brtko, Julius Ribalta, Josep Winklhofer-Roob, Brigitte Rock, Edmond Vasson, M Paule Immun Ageing Research BACKGROUND: The immune system gradually deteriorates with age and nutritional status is a major factor in immunosenescence. Of the many nutritional factors implicated in age-related immune dysfunction, vitamin A may be a good candidate, since vitamin A concentrations classically decrease during aging whereas it may possess important immunomodulatory properties via its active metabolites, the retinoic acids. This prompted us to investigate the immune response induced by retinoids in adults and elderly healthy subjects. Before and after oral supplementation with 13cis retinoic acid (0.5 mg/kg/day during 28 days), whole blood cells were phenotyped, and functions of peripheral blood mononuclear cells (PBMC) and polymorphonuclear cells (PMN) were investigated by flow cytometry and ELISA tests. RESULTS: In both young adults (n = 20, 25 ± 4 years) and older subjects (n = 20, 65 ± 4 years), retinoic acid supplementation had no effect on the distribution of leukocyte subpopulations or on the functions of PBMC (Il-2 and sIl-2R production, membrane expression of CD25). Concerning PMN, retinoic acid induced an increase in both spontaneous migration and cell surface expression of CD11b in the two different age populations, whereas bactericidal activity and phagocytosis remained unchanged. CONCLUSIONS: We demonstrated that retinoic acid induces the same intensity of immune response between adult and older subjects, and more specifically affects PMN functions, i.e. adhesion and migration, than PBMC functions. BioMed Central 2010-08-20 /pmc/articles/PMC2940875/ /pubmed/20727130 http://dx.doi.org/10.1186/1742-4933-7-10 Text en Copyright ©2010 Minet-Quinard et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Minet-Quinard, Régine
Farges, M Chantal
Thivat, Emilie
Deleine, Cécile
Mayot, Gilles
Brtko, Julius
Ribalta, Josep
Winklhofer-Roob, Brigitte
Rock, Edmond
Vasson, M Paule
Neutrophils are immune cells preferentially targeted by retinoic acid in elderly subjects
title Neutrophils are immune cells preferentially targeted by retinoic acid in elderly subjects
title_full Neutrophils are immune cells preferentially targeted by retinoic acid in elderly subjects
title_fullStr Neutrophils are immune cells preferentially targeted by retinoic acid in elderly subjects
title_full_unstemmed Neutrophils are immune cells preferentially targeted by retinoic acid in elderly subjects
title_short Neutrophils are immune cells preferentially targeted by retinoic acid in elderly subjects
title_sort neutrophils are immune cells preferentially targeted by retinoic acid in elderly subjects
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940875/
https://www.ncbi.nlm.nih.gov/pubmed/20727130
http://dx.doi.org/10.1186/1742-4933-7-10
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