Leptin induces interleukin-1β release from rat microglial cells through a caspase 1 independent mechanism

Emmanuel Pinteaux, Wataru Inoue, Lorraine Schmidt, Francisco Molina-Holgado, Nancy J. Rothwell, Giamal N. Luheshi

Research output: Contribution to journalArticlepeer-review

Abstract

Leptin regulates energy balance by suppressing appetite and increasing energy expenditure through actions in the hypothalamus. Recently we demonstrated that the effects of leptin are, at least in part, mediated by the release of interleukin (IL)-1β in the brain. Microglia constitute the major source of IL-1β in the brain but it is not known whether these cells express leptin receptors, or respond to leptin to produce IL-1β. Using RT-PCR and immunocytochemistry, we demonstrate that primary rat microglial cells express the short (non-signalling) and long (signalling) isoforms of the leptin receptors (Ob-R)s. Immunoassays performed on cell medium collected 24 h after leptin treatment (0.01-10 μg/mL) demonstrated a dose-dependent production and release of IL-1β and its endogenously occurring receptor antagonist IL-1RA. In addition leptin-induced IL-1β release occurs via a signal transducer and activator of transcription 3 (STAT3)-dependent mechanism. Western blot analysis demonstrated that leptin induced the synthesis of pro-IL-1β in microglial cells and the release of mature 17 kDa isoform into the culture medium. Leptin-induced IL-1β release was neither inhibited by the pan-caspase inhibitor BOC-D-FMK, nor by the caspase 1 inhibitor Ac-YVAD-CHO indicating that IL-1 cleavage is independent of caspase activity. These results confirm our earlier observations in vivo and demonstrate that microglia are an important source of IL-1β in the brain in response to leptin. © 2007 The Authors.
Original languageEnglish
Pages (from-to)826-833
Number of pages7
JournalJournal of neurochemistry
Volume102
Issue number3
DOIs
Publication statusPublished - Aug 2007

Keywords

  • Interleukin-1
  • Leptin
  • Microglia
  • Neuroinflammation

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