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Glucocorticoid receptor mRNA levels are selectively decreased in neutrophils of children with sepsis

OBJECTIVE: Corticosteroids are used in sepsis treatment to benefit outcome. However, discussion remains on which patients will benefit from treatment. Inter-individual variations in cortisol sensitivity, mediated through the glucocorticoid receptor, might play a role in the observed differences. Our...

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Autores principales: van den Akker, Erica L. T., Koper, Jan W., Joosten, Koen, de Jong, Frank H., Hazelzet, Jan A., Lamberts, Steven W. J., Hokken-Koelega, Anita C. S.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2698978/
https://www.ncbi.nlm.nih.gov/pubmed/19373457
http://dx.doi.org/10.1007/s00134-009-1468-6
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author van den Akker, Erica L. T.
Koper, Jan W.
Joosten, Koen
de Jong, Frank H.
Hazelzet, Jan A.
Lamberts, Steven W. J.
Hokken-Koelega, Anita C. S.
author_facet van den Akker, Erica L. T.
Koper, Jan W.
Joosten, Koen
de Jong, Frank H.
Hazelzet, Jan A.
Lamberts, Steven W. J.
Hokken-Koelega, Anita C. S.
author_sort van den Akker, Erica L. T.
collection PubMed
description OBJECTIVE: Corticosteroids are used in sepsis treatment to benefit outcome. However, discussion remains on which patients will benefit from treatment. Inter-individual variations in cortisol sensitivity, mediated through the glucocorticoid receptor, might play a role in the observed differences. Our aim was to study changes in mRNA levels of three glucocorticoid receptor splice variants in neutrophils of children with sepsis. PATIENTS AND DESIGN: Twenty-three children admitted to the pediatric intensive care unit with sepsis or septic shock were included. Neutrophils were isolated at days 0, 3 and 7, and after recovery (>3 months). mRNA levels of the glucocorticoid receptor splice variants GR-α (determining most of the cortisol effect), GR-P (increasing GR-α effect) and GR-β (inhibitor of GR-α) were measured quantitatively. MAIN RESULTS: Neutrophils from sepsis patients showed decreased levels of glucocorticoid receptor mRNA of the GR-α and GR-P splice variants on day 0 compared to after recovery. GR-α and GR-P mRNA levels showed a gradual recovery on days 3 and 7 and normalized after recovery. GR-β mRNA levels did not change significantly during sepsis. GR expression was negatively correlated to interleukin-6 (a measure of disease severity, r = −0.60, P = 0.009). CONCLUSIONS: Children with sepsis or septic shock showed a transient depression of glucocorticoid receptor mRNA in their neutrophils. This feature may represent a tissue-specific adaptation during sepsis leading to increased cortisol resistance of neutrophils. Our study adds to understanding the mechanism of cortisol sensitivity in immune cells. Future treatment strategies, aiming at timing and tissue specific regulation of glucocorticoids, might benefit patients with sepsis or septic shock.
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spelling pubmed-26989782009-06-19 Glucocorticoid receptor mRNA levels are selectively decreased in neutrophils of children with sepsis van den Akker, Erica L. T. Koper, Jan W. Joosten, Koen de Jong, Frank H. Hazelzet, Jan A. Lamberts, Steven W. J. Hokken-Koelega, Anita C. S. Intensive Care Med Original OBJECTIVE: Corticosteroids are used in sepsis treatment to benefit outcome. However, discussion remains on which patients will benefit from treatment. Inter-individual variations in cortisol sensitivity, mediated through the glucocorticoid receptor, might play a role in the observed differences. Our aim was to study changes in mRNA levels of three glucocorticoid receptor splice variants in neutrophils of children with sepsis. PATIENTS AND DESIGN: Twenty-three children admitted to the pediatric intensive care unit with sepsis or septic shock were included. Neutrophils were isolated at days 0, 3 and 7, and after recovery (>3 months). mRNA levels of the glucocorticoid receptor splice variants GR-α (determining most of the cortisol effect), GR-P (increasing GR-α effect) and GR-β (inhibitor of GR-α) were measured quantitatively. MAIN RESULTS: Neutrophils from sepsis patients showed decreased levels of glucocorticoid receptor mRNA of the GR-α and GR-P splice variants on day 0 compared to after recovery. GR-α and GR-P mRNA levels showed a gradual recovery on days 3 and 7 and normalized after recovery. GR-β mRNA levels did not change significantly during sepsis. GR expression was negatively correlated to interleukin-6 (a measure of disease severity, r = −0.60, P = 0.009). CONCLUSIONS: Children with sepsis or septic shock showed a transient depression of glucocorticoid receptor mRNA in their neutrophils. This feature may represent a tissue-specific adaptation during sepsis leading to increased cortisol resistance of neutrophils. Our study adds to understanding the mechanism of cortisol sensitivity in immune cells. Future treatment strategies, aiming at timing and tissue specific regulation of glucocorticoids, might benefit patients with sepsis or septic shock. Springer-Verlag 2009-04-17 2009-07 /pmc/articles/PMC2698978/ /pubmed/19373457 http://dx.doi.org/10.1007/s00134-009-1468-6 Text en © The Author(s) 2009
spellingShingle Original
van den Akker, Erica L. T.
Koper, Jan W.
Joosten, Koen
de Jong, Frank H.
Hazelzet, Jan A.
Lamberts, Steven W. J.
Hokken-Koelega, Anita C. S.
Glucocorticoid receptor mRNA levels are selectively decreased in neutrophils of children with sepsis
title Glucocorticoid receptor mRNA levels are selectively decreased in neutrophils of children with sepsis
title_full Glucocorticoid receptor mRNA levels are selectively decreased in neutrophils of children with sepsis
title_fullStr Glucocorticoid receptor mRNA levels are selectively decreased in neutrophils of children with sepsis
title_full_unstemmed Glucocorticoid receptor mRNA levels are selectively decreased in neutrophils of children with sepsis
title_short Glucocorticoid receptor mRNA levels are selectively decreased in neutrophils of children with sepsis
title_sort glucocorticoid receptor mrna levels are selectively decreased in neutrophils of children with sepsis
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2698978/
https://www.ncbi.nlm.nih.gov/pubmed/19373457
http://dx.doi.org/10.1007/s00134-009-1468-6
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