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Local amplifiers of IL-4Rα-mediated macrophage activation promote repair in lung and liver.

Carlos M MinuttiLucy H Jackson-JonesBelén García-FojedaJohanna A KnipperTara E SutherlandNicola LoganEmma E RingqvistRaquel Guillamat-PratsDavid A FerenbachAntonio ArtigasCordula StammeZissis C ChroneosDietmar M W ZaissCristina CasalsJudith E Allen
Published in: Science (New York, N.Y.) (2017)
The type 2 immune response controls helminth infection and maintains tissue homeostasis but can lead to allergy and fibrosis if not adequately regulated. We have discovered local tissue-specific amplifiers of type 2-mediated macrophage activation. In the lung, surfactant protein A (SP-A) enhanced interleukin-4 (IL-4)-dependent macrophage proliferation and activation, accelerating parasite clearance and reducing pulmonary injury after infection with a lung-migrating helminth. In the peritoneal cavity and liver, C1q enhancement of type 2 macrophage activation was required for liver repair after bacterial infection, but resulted in fibrosis after peritoneal dialysis. IL-4 drives production of these structurally related defense collagens, SP-A and C1q, and the expression of their receptor, myosin 18A. These findings reveal the existence within different tissues of an amplification system needed for local type 2 responses.
Keyphrases
  • peritoneal dialysis
  • immune response
  • adipose tissue
  • binding protein
  • end stage renal disease
  • transcription factor
  • signaling pathway
  • single cell
  • small molecule
  • inflammatory response
  • trypanosoma cruzi