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Transcription repressor Bach2 is required for pulmonary surfactant homeostasis and alveolar macrophage function

J Exp Med. 2013 Oct 21;210(11):2191-204. doi: 10.1084/jem.20130028. Epub 2013 Oct 14.

Abstract

Pulmonary alveolar proteinosis (PAP) results from a dysfunction of alveolar macrophages (AMs), chiefly due to disruptions in the signaling of granulocyte macrophage colony-stimulating factor (GM-CSF). We found that mice deficient for the B lymphoid transcription repressor BTB and CNC homology 2 (Bach2) developed PAP-like accumulation of surfactant proteins in the lungs. Bach2 was expressed in AMs, and Bach2-deficient AMs showed alterations in lipid handling in comparison with wild-type (WT) cells. Although Bach2-deficient AMs showed a normal expression of the genes involved in the GM-CSF signaling, they showed an altered expression of the genes involved in chemotaxis, lipid metabolism, and alternative M2 macrophage activation with increased expression of Ym1 and arginase-1, and the M2 regulator Irf4. Peritoneal Bach2-deficient macrophages showed increased Ym1 expression when stimulated with interleukin-4. More eosinophils were present in the lung and peritoneal cavity of Bach2-deficient mice compared with WT mice. The PAP-like lesions in Bach2-deficient mice were relieved by WT bone marrow transplantation even after their development, confirming the hematopoietic origin of the lesions. These results indicate that Bach2 is required for the functional maturation of AMs and pulmonary homeostasis, independently of the GM-CSF signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic-Leucine Zipper Transcription Factors / deficiency
  • Basic-Leucine Zipper Transcription Factors / metabolism*
  • Cholesterol / metabolism
  • Disease Progression
  • Dyspnea / complications
  • Dyspnea / genetics
  • Dyspnea / pathology
  • Eosinophils / metabolism
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Granulocyte-Macrophage Colony-Stimulating Factor / metabolism
  • Hematopoietic Stem Cells / metabolism
  • Homeostasis*
  • Interferon Regulatory Factors / metabolism
  • Lipid Metabolism / genetics
  • Macrophages, Alveolar / metabolism*
  • Macrophages, Peritoneal / metabolism
  • Mice
  • Phagocytosis
  • Phenotype
  • Proto-Oncogene Proteins / metabolism
  • Pulmonary Alveolar Proteinosis / complications
  • Pulmonary Alveolar Proteinosis / genetics
  • Pulmonary Alveolar Proteinosis / pathology
  • Pulmonary Surfactants / metabolism*
  • Repressor Proteins / metabolism*
  • Signal Transduction
  • Trans-Activators / metabolism

Substances

  • Bach2 protein, mouse
  • Basic-Leucine Zipper Transcription Factors
  • Interferon Regulatory Factors
  • Proto-Oncogene Proteins
  • Pulmonary Surfactants
  • Repressor Proteins
  • Trans-Activators
  • interferon regulatory factor-4
  • proto-oncogene protein Spi-1
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Cholesterol