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Cell-Autonomous Sex Differences in Gene Expression in Chicken Bone Marrow–Derived Macrophages

We have identified differences in gene expression in macrophages grown from the bone marrow of male and female chickens in recombinant chicken M-CSF (CSF1). Cells were profiled with or without treatment with bacterial LPS for 24 h. Approximately 600 transcripts were induced by prolonged LPS stimulat...

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Autores principales: Garcia-Morales, Carla, Nandi, Sunil, Zhao, Debiao, Sauter, Kristin A., Vervelde, Lonneke, McBride, Derek, Sang, Helen M., Clinton, Mike, Hume, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AAI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337484/
https://www.ncbi.nlm.nih.gov/pubmed/25637020
http://dx.doi.org/10.4049/jimmunol.1401982
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author Garcia-Morales, Carla
Nandi, Sunil
Zhao, Debiao
Sauter, Kristin A.
Vervelde, Lonneke
McBride, Derek
Sang, Helen M.
Clinton, Mike
Hume, David A.
author_facet Garcia-Morales, Carla
Nandi, Sunil
Zhao, Debiao
Sauter, Kristin A.
Vervelde, Lonneke
McBride, Derek
Sang, Helen M.
Clinton, Mike
Hume, David A.
author_sort Garcia-Morales, Carla
collection PubMed
description We have identified differences in gene expression in macrophages grown from the bone marrow of male and female chickens in recombinant chicken M-CSF (CSF1). Cells were profiled with or without treatment with bacterial LPS for 24 h. Approximately 600 transcripts were induced by prolonged LPS stimulation to an equal extent in the male and female macrophages. Many transcripts encoded on the Z chromosome were expressed ∼1.6-fold higher in males, reflecting a lack of dosage compensation in the homogametic sex. A smaller set of W chromosome–specific genes was expressed only in females. LPS signaling in mammals is associated with induction of type 1 IFN–responsive genes. Unexpectedly, because IFNs are encoded on the Z chromosome of chickens, unstimulated macrophages from the female birds expressed a set of known IFN-inducible genes at much higher levels than male cells under the same conditions. To confirm that these differences were not the consequence of the actions of gonadal hormones, we induced gonadal sex reversal to alter the hormonal environment of the developing chick and analyzed macrophages cultured from male, female, and female sex-reversed embryos. Gonadal sex reversal did not alter the sexually dimorphic expression of either sex-linked or IFN-responsive genes. We suggest that female birds compensate for the reduced dose of inducible IFN with a higher basal set point of IFN-responsive genes.
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spelling pubmed-43374842015-03-04 Cell-Autonomous Sex Differences in Gene Expression in Chicken Bone Marrow–Derived Macrophages Garcia-Morales, Carla Nandi, Sunil Zhao, Debiao Sauter, Kristin A. Vervelde, Lonneke McBride, Derek Sang, Helen M. Clinton, Mike Hume, David A. J Immunol Innate Immunity and Inflammation We have identified differences in gene expression in macrophages grown from the bone marrow of male and female chickens in recombinant chicken M-CSF (CSF1). Cells were profiled with or without treatment with bacterial LPS for 24 h. Approximately 600 transcripts were induced by prolonged LPS stimulation to an equal extent in the male and female macrophages. Many transcripts encoded on the Z chromosome were expressed ∼1.6-fold higher in males, reflecting a lack of dosage compensation in the homogametic sex. A smaller set of W chromosome–specific genes was expressed only in females. LPS signaling in mammals is associated with induction of type 1 IFN–responsive genes. Unexpectedly, because IFNs are encoded on the Z chromosome of chickens, unstimulated macrophages from the female birds expressed a set of known IFN-inducible genes at much higher levels than male cells under the same conditions. To confirm that these differences were not the consequence of the actions of gonadal hormones, we induced gonadal sex reversal to alter the hormonal environment of the developing chick and analyzed macrophages cultured from male, female, and female sex-reversed embryos. Gonadal sex reversal did not alter the sexually dimorphic expression of either sex-linked or IFN-responsive genes. We suggest that female birds compensate for the reduced dose of inducible IFN with a higher basal set point of IFN-responsive genes. AAI 2015-03-01 2015-01-30 /pmc/articles/PMC4337484/ /pubmed/25637020 http://dx.doi.org/10.4049/jimmunol.1401982 Text en Copyright © 2015 The Authors This is an open-access article distributed under the terms of the CC-BY 3.0 Unported license.
spellingShingle Innate Immunity and Inflammation
Garcia-Morales, Carla
Nandi, Sunil
Zhao, Debiao
Sauter, Kristin A.
Vervelde, Lonneke
McBride, Derek
Sang, Helen M.
Clinton, Mike
Hume, David A.
Cell-Autonomous Sex Differences in Gene Expression in Chicken Bone Marrow–Derived Macrophages
title Cell-Autonomous Sex Differences in Gene Expression in Chicken Bone Marrow–Derived Macrophages
title_full Cell-Autonomous Sex Differences in Gene Expression in Chicken Bone Marrow–Derived Macrophages
title_fullStr Cell-Autonomous Sex Differences in Gene Expression in Chicken Bone Marrow–Derived Macrophages
title_full_unstemmed Cell-Autonomous Sex Differences in Gene Expression in Chicken Bone Marrow–Derived Macrophages
title_short Cell-Autonomous Sex Differences in Gene Expression in Chicken Bone Marrow–Derived Macrophages
title_sort cell-autonomous sex differences in gene expression in chicken bone marrow–derived macrophages
topic Innate Immunity and Inflammation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337484/
https://www.ncbi.nlm.nih.gov/pubmed/25637020
http://dx.doi.org/10.4049/jimmunol.1401982
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