Adoptive Transfer of IL-33-Stimulated Macrophages into Bleomycin-Induced Mouse Models to Study Their Effect on Idiopathic Pulmonary Fibrosis In Vivo.

Abstract

The inflammatory response caused by early lung injury is one of the important causes of the development of idiopathic pulmonary fibrosis (IPF), which is accompanied by the activation of inflammatory cells such as macrophages and neutrophils, as well as the release of inflammatory factors including TNF-α, IL-1β, and IL-6. Early inflammation caused by activated pulmonary interstitial macrophages (IMs) in response to IL-33 stimulation is known to play a vital role in the pathological process of IPF. This protocol describes the adoptive transfer of IMs stimulated by IL-33 into the lungs of mice to study IPF development. It involves the isolation and culture of primary IMs from host mouse lungs, followed by the adoptive transfer of stimulated IMs into the alveoli of bleomycin (BLM)-induced IPF recipient mice (which have been previously depleted of alveolar macrophages by treatment with clodronate liposomes), and the pathological evaluation of those mice. The representative results show that the adoptive transfer of IL-33-stimulated macrophages aggravates pulmonary fibrosis in mice, suggesting that the establishment of the macrophage adoptive transfer experiment is a good technical means to study IPF pathology.

• Authors: Xiaorun Zhai, Jiao Li, Yunjuan Nie
• Journal: Journal of visualized experiments : JoVE (J Vis Exp) Issue 195 (05 05 2023) ISSN: 1940-087X [Electronic] United States
• PMID: 37212557 (Publication Type: Journal Article, Video-Audio Media, Research Support, Non-U.S. Gov't)

Chemical References

• Bleomycin
• Interleukin-33

Topics

• Mice
• Animals
• Bleomycin (adverse effects)
• Interleukin-33
• Idiopathic Pulmonary Fibrosis (chemically induced, pathology)
• Macrophages
• Lung (pathology)
• Adoptive Transfer
• Mice, Inbred C57BL