Low-intensity exercise enhances expression of markers of alternative activation in circulating leukocytes: Roles of PPARγ and Th2 cytokines
Autor: | Philip E. James, Richard Webb, Karianne Backx, Keith Morris, G. Yakeu, Lee Butcher, SA Isa, Andrew Thomas, Aled Roberts |
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Rok vydání: | 2010 |
Předmět: |
Adult
Male medicine.medical_specialty medicine.medical_treatment CD14 Inflammation Physical exercise Th2 Cells Downregulation and upregulation Internal medicine Leukocytes medicine Humans Interleukin 6 Exercise biology business.industry Macrophages Cell Differentiation Middle Aged M2 Macrophage Interleukin-10 PPAR gamma Interleukin 10 Phenotype Endocrinology Cytokine Gene Expression Regulation Immunology biology.protein Female Interleukin-4 medicine.symptom Cardiology and Cardiovascular Medicine business |
Zdroj: | Atherosclerosis. 212:668-673 |
ISSN: | 0021-9150 |
DOI: | 10.1016/j.atherosclerosis.2010.07.002 |
Popis: | Objective Pharmacological activation of the nuclear receptor PPARγ is linked to numerous beneficial effects in the contexts of inflammation, lipid homeostasis, Type-2 Diabetes (T2D) and atherosclerosis. These beneficial effects include priming of circulating monocytes for differentiation towards an ‘alternative’ anti-inflammatory M2 macrophage phenotype. As we have recently shown that participation in low-intensity exercise increases PPARγ expression and activity in leukocytes from previously sedentary individuals, we aimed to elucidate whether low-intensity exercise elicited a pattern of gene expression similar to that reported for M2 monocyte-macrophage differentiation. Methods 17 sedentary individuals undertook an 8-week low-intensity exercise programme (walking 10,000 steps/day, three times/week). Changes in expression of PPARs and the PPARγ co-activators PGC-1α and PGC-1β; Th2 (IL-4; IL-10) and Th1 (IL-6) cytokines; and markers for the M2 (AMAC1, CD14, MR, IL-4) and the ‘classical’ pro-inflammatory M1 (MCP-1, TNFα, IL-6) phenotypes, were determined using RT-PCR (to assess leukocyte mRNA expression) and ELISA (to assess plasma cytokine levels). Results Exercise was associated with upregulation of M2 markers, PGC-1α and PGC-1β, and with downregulation of M1 markers. Moreover, plasma levels of Th2 cytokines increased after exercise, while those of Th1 cytokines decreased. However, other PPARs (PPARα; PPARβ/δ) did not undergo marked exercise-induced activation or upregulation. Thus, participation in low-intensity exercise may prime monocytes for differentiation towards an M2 macrophage phenotype via PPARγ/PGC-1α/β. Conclusion Given the similarities between these effects and pharmacologically induced M2 polarisation, we propose that exercise-induced PPARγ/PGC-1α/β-mediated M2 polarisation may constitute a novel anti-inflammatory benefit of low-intensity exercise. |
Databáze: | OpenAIRE |
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