Rac2 is required for alternative macrophage activation and bleomycin induced pulmonary fibrosis; a macrophage autonomous phenotype

Shweta Joshi, Alok R. Singh, Simon S. Wong, Muamera Zulcic, Min Jiang, Annie Pardo, Moises Selman, James S. Hagood, Donald L. Durden

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease characterized by cellular phenotype alterations and deposition of extracellular matrix proteins. The alternative activation of macrophages in the lungs has been associated as a major factor promoting pulmonary fibrosis, however the mechanisms underlying this phenomenon are poorly understood. In the present study, we have defined a molecular mechanism by which signals transmitted from the extracellular matrix via the α4β1 integrin lead to the activation of Rac2 which regulates alternative macrophage differentiation, a signaling axis within the pulmonary macrophage compartment required for bleomycin induced pulmonary fibrosis. Mice deficient in Rac2 were protected against bleomycin-induced fibrosis and displayed diminished collagen deposition in association with lower expression of alternatively activated profibrotic macrophage markers. We have demonstrated a macrophage autonomous process by which the injection of M2 and not M1 macrophages restored the bleomycin induced pulmonary fibrosis susceptibility in Rac2-/- mice, establishing a critical role for a macrophage Rac2 signaling axis in the regulation of macrophage differentiation and lung fibrosis in vivo. We also demonstrate that markers of alternative macrophage activation are increased in patients with IPF. Taken together, these studies define an important role for an integrin-driven Rac2 signaling axis in macrophages, and reveal that Rac2 activation is required for polarization of macrophages towards a profibrotic phenotype and progression of pulmonary fibrosis in vivo.

Original languageEnglish (US)
Article numbere0182851
JournalPloS one
Volume12
Issue number8
DOIs
StatePublished - Aug 2017

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macrophage activation
Macrophage Activation
Pulmonary Fibrosis
Macrophages
Bleomycin
fibrosis
macrophages
Chemical activation
lungs
Phenotype
phenotype
Idiopathic Pulmonary Fibrosis
integrins
Integrins
extracellular matrix
Fibrosis
Lung
Extracellular Matrix Proteins
Alveolar Macrophages
Pulmonary diseases

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)
  • General

Cite this

Rac2 is required for alternative macrophage activation and bleomycin induced pulmonary fibrosis; a macrophage autonomous phenotype. / Joshi, Shweta; Singh, Alok R.; Wong, Simon S.; Zulcic, Muamera; Jiang, Min; Pardo, Annie; Selman, Moises; Hagood, James S.; Durden, Donald L.

In: PloS one, Vol. 12, No. 8, e0182851, 08.2017.

Research output: Contribution to journalArticle

Joshi, S, Singh, AR, Wong, SS, Zulcic, M, Jiang, M, Pardo, A, Selman, M, Hagood, JS & Durden, DL 2017, 'Rac2 is required for alternative macrophage activation and bleomycin induced pulmonary fibrosis; a macrophage autonomous phenotype', PloS one, vol. 12, no. 8, e0182851. https://doi.org/10.1371/journal.pone.0182851
Joshi, Shweta ; Singh, Alok R. ; Wong, Simon S. ; Zulcic, Muamera ; Jiang, Min ; Pardo, Annie ; Selman, Moises ; Hagood, James S. ; Durden, Donald L. / Rac2 is required for alternative macrophage activation and bleomycin induced pulmonary fibrosis; a macrophage autonomous phenotype. In: PloS one. 2017 ; Vol. 12, No. 8.
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