TY - JOUR
T1 - Contrasting effects of western vs. Mediterranean diets on monocyte inflammatory gene expression and social behavior in a primate model
AU - Johnson, Corbin S.C.
AU - Shively, Carol A.
AU - Michalson, Kristofer T.
AU - Lea, Amanda J.
AU - Debo, Ryne J.
AU - Howard, Timothy D.
AU - Hawkins, Gregory A.
AU - Appt, Susan E.
AU - Liu, Yongmei
AU - McCall, Charles E.
AU - Herrington, David M.
AU - Ip, Edward H.
AU - Register, Thomas C.
AU - Snyder-Mackler, Noah
N1 - Funding Information:
Shared Resource is supported by P30CA012197 and by a NIH Shared Instrumentation Grant
Funding Information:
R01AG060931 from NIH, and AJL was supported by a postdoctoral fellowship from the Helen
Funding Information:
Funding: This work was funded by R01HL087103 (CAS), R01HL122393 (TCR),
Funding Information:
This work was funded by R01HL087103 (CAS), R01HL122393 (TCR), U24DK097748 (TCR) from NIH and intramural funding from the Department of Pathology, Wake Forest School of Medicine (CAS). NSM was supported by R00AG051764 and R01AG060931 from NIH, and AJL was supported by a postdoctoral fellowship from the Helen Hay Whitney Foundation. The Wake Forest Comprehensive Cancer Center Cancer Genomics Shared Resource is supported by P30CA012197 and by a NIH Shared Instrumentation Grant S10OD023409 to GAH.
Funding Information:
U24DK097748 (TCR) from NIH and intramural funding from the Department of Pathology,
Funding Information:
Wake Forest School of Medicine (CAS). NSM was supported by R00AG051764 and
Publisher Copyright:
© 2021, eLife Sciences Publications Ltd. All rights reserved.
PY - 2021
Y1 - 2021
N2 - Dietary changes associated with industrialization substantially increase the prevalence of chronic diseases, such as obesity, type II diabetes, and cardiovascular disease, major contributors to the public health burden. The high prevalence of these chronic diseases is often attributed to an “evolutionary mismatch” between human physiology and modern nutritional environments. Western diets enriched with foods that were scarce throughout human evolutionary history (e.g., simple sugars and saturated fats) promote inflammation and disease relative to diets more akin to ancestral human hunter-gatherer diets, such as a Mediterranean diet. Peripheral blood monocytes, precursors to macrophages and important mediators of innate immunity and inflammation, are sensitive to the environment and may represent a critical intermediate in the pathway linking diet to disease. We evaluated the effects of 15 months of whole diet manipulations mimicking human Western or Mediterranean diet patterns on monocyte polarization using a well-established model of human health, the cynomolgus macaque (Macaca fascicularis). Monocyte transcriptional profiles differed markedly between the two diets, with 40% of transcripts showing differential expression (FDR < 0.05). Monocytes from Western diet consumers were polarized toward a more proinflammatory phenotype. Compared to the Mediterranean diet, the Western diet shifted the co-expression of 445 gene pairs, including small RNAs and transcription factors associated with metabolism and adiposity in humans, and dramatically altered behavior. For example, Western-fed individuals were more anxious and less socially integrated compared to the Mediterranean-fed subjects. These behavioral changes were also associated with some of the effects of diet on gene expression, suggesting an interaction between diet, central nervous system activity, and monocyte gene expression. The results of this study provide new insights into evolutionary mismatch at the molecular level and uncover new pathways through which Western diets alter monocyte polarization toward a proinflammatory phenotype.
AB - Dietary changes associated with industrialization substantially increase the prevalence of chronic diseases, such as obesity, type II diabetes, and cardiovascular disease, major contributors to the public health burden. The high prevalence of these chronic diseases is often attributed to an “evolutionary mismatch” between human physiology and modern nutritional environments. Western diets enriched with foods that were scarce throughout human evolutionary history (e.g., simple sugars and saturated fats) promote inflammation and disease relative to diets more akin to ancestral human hunter-gatherer diets, such as a Mediterranean diet. Peripheral blood monocytes, precursors to macrophages and important mediators of innate immunity and inflammation, are sensitive to the environment and may represent a critical intermediate in the pathway linking diet to disease. We evaluated the effects of 15 months of whole diet manipulations mimicking human Western or Mediterranean diet patterns on monocyte polarization using a well-established model of human health, the cynomolgus macaque (Macaca fascicularis). Monocyte transcriptional profiles differed markedly between the two diets, with 40% of transcripts showing differential expression (FDR < 0.05). Monocytes from Western diet consumers were polarized toward a more proinflammatory phenotype. Compared to the Mediterranean diet, the Western diet shifted the co-expression of 445 gene pairs, including small RNAs and transcription factors associated with metabolism and adiposity in humans, and dramatically altered behavior. For example, Western-fed individuals were more anxious and less socially integrated compared to the Mediterranean-fed subjects. These behavioral changes were also associated with some of the effects of diet on gene expression, suggesting an interaction between diet, central nervous system activity, and monocyte gene expression. The results of this study provide new insights into evolutionary mismatch at the molecular level and uncover new pathways through which Western diets alter monocyte polarization toward a proinflammatory phenotype.
KW - Affiliative behavior
KW - Anxiety-associated behavior
KW - Differential gene co-expression
KW - Immune regulation
KW - Inflammatory gene expression
KW - Mediterranean diet
KW - Monocyte polarization
KW - Social isolation
KW - Western diet
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U2 - 10.7554/ELIFE.68293
DO - 10.7554/ELIFE.68293
M3 - Article
C2 - 34338633
AN - SCOPUS:85112395966
SN - 2050-084X
VL - 10
JO - eLife
JF - eLife
M1 - e68293
ER -