Elective orthopedic surgery, a model for the study of cytokine activation and regulation

Citation
M. Van Deuren et al., Elective orthopedic surgery, a model for the study of cytokine activation and regulation, CYTOKINE, 10(11), 1998, pp. 897-903
Citations number
51
Categorie Soggetti
Cell & Developmental Biology
Journal title
CYTOKINE
ISSN journal
10434666 → ACNP
Volume
10
Issue
11
Year of publication
1998
Pages
897 - 903
Database
ISI
SICI code
1043-4666(199811)10:11<897:EOSAMF>2.0.ZU;2-P
Abstract
Induction and downregulation of cytokine production occurs after contact wi th various inflammatory stimuli. To elucidate the early events after a phys ical stressor, we studied these processes in 13 patients undergoing electiv e total hip replacement surgery. In these patients we followed the plasma c oncentrations of tumour necrosis factor alpha (TNF), interleukin 1 beta (IL -1 beta), IL-6 and IL-1 receptor antagonist (IL-1Ra), mRNA for these cytoki nes in peripheral blood cells (PBCs), and the lipopolysaccharide(LPS) -stim ulated ex vivo production of these cytokines in whole blood cultures (WBCs) . Plasma TNF and IL-1 beta were not affected by the surgical procedure, alt hough IL-1 beta mRNA levels in PBCs increased significantly. Plasma IL-6 and IL-1Ra increased from 2 to 3h post-incision onwards. The LP S-induced ex vivo production in WBCs of TNF, IL-1 beta and IL-6 decreased f rom 2 h post-incision; that of IL-1Ra increased. Downregulation of TNF prod uction was not associated with lower TNF-mRNA suggesting post-transcription al regulatory processes. In contrast, downregulation of IL-1 beta productio n was associated with significantly lower IL-1 beta mRNA, suggesting both p ost-transcriptional and transcriptional mechanisms. Remarkably, the increas e of plasma IL-6 occurred when the IL-6 production ex-vivo in WBCs was maxi mally downregulated. This suggests that other immunocompetent cells and not PBCs are the source for plasma IL-6 and that the IL-6 production in those other cells might be regulated differentially.