Circulating interleukin-6 induces fever through a STAT3-linked activation of COX-2 in the brain

1 Douglas Hospital Research Centre, Department of Psychiatry, McGill University, Montreal, Quebec, Canada; and 2 Department of Endocrinology, National Institute for Biological Standards and Control, Potters Bar, United Kingdom Submitted 5 May 2006 ; accepted in final form 27 June 2006 Interleukin (IL)-6 is an important humoral mediator of fever following infection and inflammation and satisfies a number of criteria for a circulating pyrogen. However, evidence supporting such a role is diminished by the moderate or even absent ability of the recombinant protein to induce fever and activate the cyclooxygenase-2 (COX-2) pathway in the brain, a prerequisite step in the initiation and maintenance of fever. In the present study, we investigated the role of endogenous circulating IL-6 in a rodent model of localized inflammation, by neutralizing its action using a specific antiserum (IL-6AS). Rats were injected with LPS (100 µg/kg) or saline into a preformed air pouch in combination with an intraperitoneal injection of either normal sheep serum or IL-6AS (1.8 ml/rat). LPS induced a febrile response, which was accompanied by a significant rise in plasma IL-6 and nuclear STAT3 translocation in endothelial cells throughout the brain 2 h after treatment, including areas surrounding the sensory circumventricular organs and the median preoptic area (MnPO), important regions in mediating fever. These responses were abolished in the presence of the IL-6AS, which also significantly inhibited the LPS-induced upregulation of mRNA expression or immunoreactivity (IR) of the inducible form of COX, the rate-limiting enzyme for PGE 2 -synthesis. Interestingly, nuclear signal transducer and activator of transcription (STAT)3-positive cells colocalized with COX-2-IR, signifying that IL-6-activated cells are directly involved in PGE 2 production. These observations suggest that IL-6 is an important circulating pyrogen that activates the COX-2-pathway in cerebral microvasculature, most likely through a STAT3-dependent pathway. local inflammation; cytokines; nuclear factor- B; prostaglandins; circumventricular organs Address for reprint requests and other correspondence: G. N. Luheshi, Douglas Hospital Research Centre, Dept. of Psychiatry, McGill Univ., 6875 Blvd. LaSalle, Verdun, Montreal, QC, H4H 1R3, Canada (e-mail: giamal.luheshi{at}mcgill.ca )