Wnt/β-catenin signaling regulates lipopolysaccharide-altered polarizations of RAW264.7 cells and alveolar macrophages in mouse lungs
Introduction Macrophages are capable of exerting both proinflammatory and anti-inflammatory functions in response to distinct environmental stimuli, by polarizing into classically inflammatory state (M1) and anti-inflammatory phenotype (M2), respectively. The Wnt/β-catenin signaling plays an importa...
Main Authors: | , , , , , , , , , |
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Format: | Article |
Language: | English |
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SAGE Publishing
2021-11-01
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Series: | European Journal of Inflammation |
Online Access: | https://doi.org/10.1177/20587392211059362 |
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author | Jiali Yang Ying Wang Dandan Yang Jia Ma Shuang Wu Qian Cai Jing Xue Chao Yuan Jing Wang Xiaoming Liu |
author_facet | Jiali Yang Ying Wang Dandan Yang Jia Ma Shuang Wu Qian Cai Jing Xue Chao Yuan Jing Wang Xiaoming Liu |
author_sort | Jiali Yang |
collection | DOAJ |
description | Introduction Macrophages are capable of exerting both proinflammatory and anti-inflammatory functions in response to distinct environmental stimuli, by polarizing into classically inflammatory state (M1) and anti-inflammatory phenotype (M2), respectively. The Wnt/β-catenin signaling plays an important role in the tissue homeostasis and immune regulations, including the macrophage polarizations. However, the molecular mechanism of Wnt/β-catenin signaling in regulating alveolar macrophage polarization in an inflammatory state remains unclear. Methods The Wnt/β-catenin signaling-altered phenotypes of murine macrophage-like RAW264.7 cells in vitro and alveolar macrophage in vivo in both of naïve and lipopolysaccharide-induced inflammation states were accessed by immunoblotting and immunostaining assays. Results The activation of Wnt/β-catenin signaling inhibited macrophage M1 polarization, but promoted alternative M2 polarization in murine RAW264.7 cells under a naïve state. Interestingly, in an LPS-induced inflammation condition, the enhanced Wnt/β-catenin activity suppressed both M1 and M2 polarizations in RAW264.7 cells in vitro, and primary alveolar macrophages of LPS-challenged mice in vivo . Molecular analysis further demonstrated an involvement of Stat signing in regulating Wnt/β-catenin signaling-altered polarizations in mouse alveolar macrophages. Conclusion These results suggest a mechanism by which Wnt/β-catenin signaling modulates macrophage polarization in an inflammation state by regulating the Stat signaling pathway. |
first_indexed | 2024-12-14T09:02:45Z |
format | Article |
id | doaj.art-be4060b9588b40b680c100c9218e9727 |
institution | Directory Open Access Journal |
issn | 2058-7392 |
language | English |
last_indexed | 2024-12-14T09:02:45Z |
publishDate | 2021-11-01 |
publisher | SAGE Publishing |
record_format | Article |
series | European Journal of Inflammation |
spelling | doaj.art-be4060b9588b40b680c100c9218e97272022-12-21T23:08:47ZengSAGE PublishingEuropean Journal of Inflammation2058-73922021-11-011910.1177/20587392211059362Wnt/β-catenin signaling regulates lipopolysaccharide-altered polarizations of RAW264.7 cells and alveolar macrophages in mouse lungsJiali YangYing WangDandan YangJia MaShuang WuQian CaiJing XueChao YuanJing WangXiaoming LiuIntroduction Macrophages are capable of exerting both proinflammatory and anti-inflammatory functions in response to distinct environmental stimuli, by polarizing into classically inflammatory state (M1) and anti-inflammatory phenotype (M2), respectively. The Wnt/β-catenin signaling plays an important role in the tissue homeostasis and immune regulations, including the macrophage polarizations. However, the molecular mechanism of Wnt/β-catenin signaling in regulating alveolar macrophage polarization in an inflammatory state remains unclear. Methods The Wnt/β-catenin signaling-altered phenotypes of murine macrophage-like RAW264.7 cells in vitro and alveolar macrophage in vivo in both of naïve and lipopolysaccharide-induced inflammation states were accessed by immunoblotting and immunostaining assays. Results The activation of Wnt/β-catenin signaling inhibited macrophage M1 polarization, but promoted alternative M2 polarization in murine RAW264.7 cells under a naïve state. Interestingly, in an LPS-induced inflammation condition, the enhanced Wnt/β-catenin activity suppressed both M1 and M2 polarizations in RAW264.7 cells in vitro, and primary alveolar macrophages of LPS-challenged mice in vivo . Molecular analysis further demonstrated an involvement of Stat signing in regulating Wnt/β-catenin signaling-altered polarizations in mouse alveolar macrophages. Conclusion These results suggest a mechanism by which Wnt/β-catenin signaling modulates macrophage polarization in an inflammation state by regulating the Stat signaling pathway.https://doi.org/10.1177/20587392211059362 |
spellingShingle | Jiali Yang Ying Wang Dandan Yang Jia Ma Shuang Wu Qian Cai Jing Xue Chao Yuan Jing Wang Xiaoming Liu Wnt/β-catenin signaling regulates lipopolysaccharide-altered polarizations of RAW264.7 cells and alveolar macrophages in mouse lungs European Journal of Inflammation |
title | Wnt/β-catenin signaling regulates lipopolysaccharide-altered polarizations of RAW264.7 cells and alveolar macrophages in mouse lungs |
title_full | Wnt/β-catenin signaling regulates lipopolysaccharide-altered polarizations of RAW264.7 cells and alveolar macrophages in mouse lungs |
title_fullStr | Wnt/β-catenin signaling regulates lipopolysaccharide-altered polarizations of RAW264.7 cells and alveolar macrophages in mouse lungs |
title_full_unstemmed | Wnt/β-catenin signaling regulates lipopolysaccharide-altered polarizations of RAW264.7 cells and alveolar macrophages in mouse lungs |
title_short | Wnt/β-catenin signaling regulates lipopolysaccharide-altered polarizations of RAW264.7 cells and alveolar macrophages in mouse lungs |
title_sort | wnt β catenin signaling regulates lipopolysaccharide altered polarizations of raw264 7 cells and alveolar macrophages in mouse lungs |
url | https://doi.org/10.1177/20587392211059362 |
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