Exertional heat stroke leads to concurrent long-term epigenetic memory, immunosuppression and altered heat shock response in female mice.
Kevin O MurrayJason O BrantJohn D IwaniecLaila H SheikhLucas de CarvalhoChristian K GarciaGerard P RobinsonJamal M AlzahraniAlberto RivaOrlando LaitanoMichael P KladdeThomas L ClantonPublished in: The Journal of physiology (2020)
Exposure to exertional heat stroke (EHS) has been linked to increased susceptibility to a second heat stroke, infection and cardiovascular disease. Whether these clinical outcomes are mediated by an epigenetic memory is unknown. Using a preclinical mouse model of EHS, we investigated whether EHS exposure produces a lasting epigenetic memory in monocytes and whether there are phenotypic alterations that may be consistent with these epigenetic changes. Female mice underwent forced wheel running at 37.5°C/40% relative humidity until symptom limitation, characterized by CNS dysfunction. Results were compared with matched exercise controls at 22.5°C. Monocytes were isolated from bone marrow after 4 or 30 days of recovery to extract DNA and analyse methylation. Broad-ranging alterations to the DNA methylome were observed at both time points. At 30 days, very specific alterations were observed to the promoter regions of genes involved with immune responsiveness. To test whether these changes might be related to phenotype, whole blood at 30 days was challenged with lipopolysaccharide (LPS) to measure cytokine secretion; monocytes were also challenged with heat shock to quantify mRNA expression. Whole blood collected from EHS mice showed markedly attenuated inflammatory responses to LPS challenge. Furthermore, monocyte mRNA from EHS mice showed significantly altered responses to heat shock challenge. These results demonstrate that EHS leads to a unique DNA methylation pattern in monocytes and altered immune and heat shock responsiveness after 30 days. These data support the hypothesis that EHS exposure can induce long-term physiological changes that may be linked to altered epigenetic profiles.
Keyphrases
- heat shock
- heat stress
- dna methylation
- gene expression
- genome wide
- high fat diet induced
- heat shock protein
- cardiovascular disease
- dendritic cells
- oxidative stress
- atrial fibrillation
- working memory
- peripheral blood
- bone marrow
- inflammatory response
- mouse model
- single molecule
- circulating tumor
- squamous cell carcinoma
- toll like receptor
- anti inflammatory
- blood brain barrier
- metabolic syndrome
- type diabetes
- coronary artery disease
- high intensity
- endothelial cells
- wild type
- copy number
- radiation therapy
- high resolution
- big data
- insulin resistance
- physical activity
- deep learning
- cardiovascular events
- electronic health record
- adipose tissue