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Updated: Jul 28, 2026

Investigation of Macrophage Polarization Using Bone Marrow Derived Macrophages
Published on: June 23, 2013
Regulation of macrophage gene expression by the peroxisome proliferator-activated receptor-gamma
M Ricote1, J S Welch, C K Glass
1Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA 92093-0651, USA. mricote@ucsd.edu
Abstract:
The peroxisome proliferator-activated receptor-gamma (PPAR-gamma), which is a member of the nuclear hormone receptor superfamily and was originally shown to play an important role in adipocyte differentiation and glucose homeostasis, is now known to regulate cellular proliferation and inflammatory responses. A range of synthetic and naturally occurring substances activates PPAR-gamma, however the identities of endogenous ligands for PPAR-gamma and their means of production in vivo have not been well established. In monocytes and macrophages, interleukin-4 (IL-4) increases the expression of 12/15-lipoxygenase and thus 13-HODE and 15-HETE production. We show that IL-4 induces the expression of PPAR-gamma and provide evidence that the coordinate induction of PPAR-gamma and 12/15-lipoxygenase mediates IL-4 dependent transcription of the CD36 gene and down-regulation of iNOS in macrophages. These findings suggest that PPAR-gamma activity may play an important role in mediating macrophage gene expression signaled by IL-4.
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