Social stress up-regulates inflammatory gene expression in the leukocyte transcriptome via β-adrenergic induction of myelopoiesis

Across a variety of adverse life circumstances, such as social isolation and low socioeconomic status, mammalian immune cells have been found to show a conserved transcriptional response to adversity (CTRA) involving increased expression of proinflammatory genes. The present study examines whether s...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS Jg. 110; H. 41; S. 16574
Hauptverfasser: Powell, Nicole D, Sloan, Erica K, Bailey, Michael T, Arevalo, Jesusa M G, Miller, Gregory E, Chen, Edith, Kobor, Michael S, Reader, Brenda F, Sheridan, John F, Cole, Steven W
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States 08.10.2013
Schlagworte:
Animals
Computational Biology
Flow Cytometry
Gene Expression Profiling
Gene Expression Regulation - physiology
Granulocyte-Macrophage Colony-Stimulating Factor - metabolism
Humans
Male
Mice
Mice, Inbred C57BL
Monocytes - metabolism
Myelopoiesis - physiology
Propranolol
Receptors, Adrenergic, beta - metabolism
Social Environment
Socioeconomic Factors
Stress, Psychological - metabolism
Sympathetic Nervous System - physiology
Transcription Factors - metabolism
Transcriptome - genetics
social genomics
immunology
ISSN:1091-6490, 1091-6490
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Zusammenfassung:Across a variety of adverse life circumstances, such as social isolation and low socioeconomic status, mammalian immune cells have been found to show a conserved transcriptional response to adversity (CTRA) involving increased expression of proinflammatory genes. The present study examines whether such effects might stem in part from the selective up-regulation of a subpopulation of immature proinflammatory monocytes (Ly-6c(high) in mice, CD16(-) in humans) within the circulating leukocyte pool. Transcriptome representation analyses showed relative expansion of the immature proinflammatory monocyte transcriptome in peripheral blood mononuclear cells from people subject to chronic social stress (low socioeconomic status) and mice subject to repeated social defeat. Cellular dissection of the mouse peripheral blood mononuclear cell transcriptome confirmed these results, and promoter-based bioinformatic analyses indicated increased activity of transcription factors involved in early myeloid lineage differentiation and proinflammatory effector function (PU.1, NF-κB, EGR1, MZF1, NRF2). Analysis of bone marrow hematopoiesis confirmed increased myelopoietic output of Ly-6c(high) monocytes and Ly-6c(intermediate) granulocytes in mice subject to repeated social defeat, and these effects were blocked by pharmacologic antagonists of β-adrenoreceptors and the myelopoietic growth factor GM-CSF. These results suggest that sympathetic nervous system-induced up-regulation of myelopoiesis mediates the proinflammatory component of the leukocyte CTRA dynamic and may contribute to the increased risk of inflammation-related disease associated with adverse social conditions.
Bibliographie:ObjectType-Article-1
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ISSN:1091-6490
1091-6490
DOI:10.1073/pnas.1310655110