Differential expression of FIZZ1 and Ym1 in alternatively versus classically activated macrophages

J Leukoc Biol. 2002 Apr;71(4):597-602.


Alternatively activated macrophages (aaMphi) display molecular and biological characteristics that differ from those of classically activated macrophages (caMphi). Recently, we described an experimental model of murine trypanosomosis in which the early stage of infection of mice with a Trypanosoma brucei brucei variant is characterized by the development of caMphi, whereas in the late and chronic stages of infection, aaMphi develop. In the present study, we used suppression subtractive hybridization (SSH) to identify genes that are expressed differentially in aaMphi versus caMphi elicited during infection with this T. b. brucei variant. We show that FIZZ1 and Ym1 are induced strongly in in vivo- and in vitro-elicited aaMphi as compared with caMphi. Furthermore, we demonstrate that the in vivo induction of FIZZ1 and Ym1 in macrophages depends on IL-4 and that in vitro, IFN-gamma antagonizes the effect of IL-4 on the expression of FIZZ1 and Ym1. Collectively, these results open perspectives for new insights into the functional properties of aaMphi and establish FIZZ1 and Ym1 as markers for aaMphi.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Female
  • Gene Expression Regulation* / drug effects
  • Gene Library
  • Intercellular Signaling Peptides and Proteins
  • Interferon-alpha / pharmacology
  • Interleukin-4 / pharmacology
  • Lectins / genetics*
  • Macrophage Activation*
  • Macrophages / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Nerve Growth Factor
  • Nucleic Acid Hybridization
  • Proteins / genetics*
  • Trypanosomiasis, African / immunology
  • Type C Phospholipases / physiology
  • beta-N-Acetylhexosaminidases*


  • Intercellular Signaling Peptides and Proteins
  • Interferon-alpha
  • Lectins
  • Proteins
  • Retnla protein, mouse
  • Interleukin-4
  • Nerve Growth Factor
  • Type C Phospholipases
  • Chil3 protein, mouse
  • beta-N-Acetylhexosaminidases