Year: 2008
Type: article
Abstract: An emerging body of evidence supports a relationship between the circadian and immune systems during an innate immune response.Previously, we have demonstrated synchronized upregulation of core circadian clock genes, Per2 and Bmal1, in equine whole blood following lipopolysaccharide (LPS) administration in vivo.Subsequent experiments suggested a role for the febrile mediator, prostaglandin E 2 (PGE 2 ), in mediating this response.However, PGE 2 failed to directly stimulate clock gene expression in equine PBMCs.This study demonstrates that ex vivo cultured equine neutrophils actively respond to PGE 2 by upregulating Per2 and Bmal1 expression.In addition, we show that LPS induces marked neutrophilia and concomitant monocytopenia in equine peripheral blood at the time corresponding to the previously observed clock gene rise.We further report that the peak in the PGE 2 mediated endotoxic fever also occurs simultaneously.Combined, our data suggest that neutrophils are the source of the rise in Per2 and Bmal1 expression previously observed in equine peripheral blood following LPS administration, and that this response is likely mediated by PGE 2 .These results provide the first evidence for a potential role of core circadian clock genes in neutrophil function following innate immune activation.
Institutions: University College Dublin, University of Kentucky
Language: English
Subfield: Endocrine and Autonomic Systems
Field: Neuroscience
Domain: Life Sciences
Open Access status: bronze
Funder: University of Kentucky
OpenAlex ID: W2117329859
