Fas determines differential fates of resident and recruited macrophages during resolution of acute lung injury

William J. Janssen, Lea Barthel, Alaina Muldrow, Rebecca E. Oberley-Deegan, Mark T. Kearns, Claudia Jakubzick, Peter M. Henson

Research output: Contribution to journalArticle

160 Scopus citations

Abstract

Rationale: During acute lung injury (ALI) the macrophage pool expands markedly as inflammatory monocytes migrate from the circulation to the airspaces. As inflammation resolves, macrophage numbers return to preinjury levels and normal tissue structure and function are restored. Objectives: To determine the fate of resident and recruited macrophages during the resolution of ALI in mice and to elucidate the mechanisms responsible for macrophage removal. Methods: ALI was induced in mice using influenza A (H1N1; PR8) infection and LPS instillation. Dye labeling techniques, bone marrow transplantation, and surface immunophenotyping were used to distinguish resident and recruited macrophages during inflammation and to study the role of Fas in determining macrophage fate during resolving ALI. Measurements and Main Results: During acute and resolving lung injury from influenza A and LPS, a high proportion of the original resident alveolar macrophages persisted. In contrast, recruited macrophages exhibited robust accumulation in early inflammation, followed by a progressive decline in their number. This decline was mediated by apoptosis with local phagocytic clearance. Recruited macrophages expressed high levels of the death receptor Fas and were rapidly depleted from the airspaces by Fas-activating antibodies. In contrast, macrophage depletion was inhibited in mice treated with Fas-blocking antibodies and in chimeras with Fasdeficient bone marrow. Caspase-8 inhibition preventedmacrophage apoptosis and delayed the resolution of ALI. Conclusions: These findings indicate that Fas-induced apoptosis of recruitedmacrophages is essential for complete resolution of ALI.

Original languageEnglish (US)
Pages (from-to)547-560
Number of pages14
JournalAmerican Journal of Respiratory and Critical Care Medicine
Volume184
Issue number5
DOIs
StatePublished - Sep 1 2011

Keywords

  • Apoptosis
  • Inflammation
  • Monocyte

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine
  • Critical Care and Intensive Care Medicine

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