PCLAF-DREAM drives alveolar cell plasticity for lung regeneration

Cell plasticity, changes in cell fate, is crucial for tissue regeneration. In the lung, failure of regeneration leads to diseases, including fibrosis. However, the mechanisms governing alveolar cell plasticity during lung repair remain elusive. We previously showed that PCLAF remodels the DREAM complex, shifting the balance from cell quiescence towards cell proliferation. Here, we find that PCLAF expression is specific to proliferating lung progenitor cells, along with the DREAM target genes transactivated by lung injury. Genetic ablation of Pclaf impairs AT1 cell repopulation from AT2 cells, leading to lung fibrosis. Mechanistically, the PCLAF-DREAM complex transactivates CLIC4, triggering TGF-β signaling activation, which promotes AT1 cell generation from AT2 cells. Furthermore, phenelzine that mimics the PCLAF-DREAM transcriptional signature increases AT2 cell plasticity, preventing lung fibrosis in organoids and mice. Our study reveals the unexpected role of the PCLAF-DREAM axis in promoting alveolar cell plasticity, beyond cell proliferation control, proposing a potential therapeutic avenue for lung fibrosis prevention.

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Publication Details

Journal
Nature Communications
Published
2024-10-24
DOI
https://doi.org/10.1038/s41467-024-53330-1
Citations
16
Primary Topic
Neonatal Respiratory Health Research
Type
article
Field-Weighted Citation Impact
6.70

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article

PCLAF-DREAM drives alveolar cell plasticity for lung regeneration

Shengzhe Zhang, Lisandra Vila Ellis, Kyung-Pil Ko, Jichao Chen et al.
16 citations
Nature Communications
Neonatal Respiratory Health Research
6.70
article

PCLAF-DREAM drives alveolar cell plasticity for lung regeneration

Shengzhe Zhang, Lisandra Vila Ellis, Kyung-Pil Ko, Jichao Chen, Jae‐Il Park, Gengyi Zou, Bong-Jun Kim, Moon Jong Kim, Margherita Paschini, Carla F. Kim, Danielle Little, Jie Zhang, Yuanjian Huang, Sohee Jun
article en
16 citations

Abstract

Cell plasticity, changes in cell fate, is crucial for tissue regeneration. In the lung, failure of regeneration leads to diseases, including fibrosis. However, the mechanisms governing alveolar cell plasticity during lung repair remain elusive. We previously showed that PCLAF remodels the DREAM complex, shifting the balance from cell quiescence towards cell proliferation. Here, we find that PCLAF expression is specific to proliferating lung progenitor cells, along with the DREAM target genes transactivated by lung injury. Genetic ablation of Pclaf impairs AT1 cell repopulation from AT2 cells, leading to lung fibrosis. Mechanistically, the PCLAF-DREAM complex transactivates CLIC4, triggering TGF-β signaling activation, which promotes AT1 cell generation from AT2 cells. Furthermore, phenelzine that mimics the PCLAF-DREAM transcriptional signature increases AT2 cell plasticity, preventing lung fibrosis in organoids and mice. Our study reveals the unexpected role of the PCLAF-DREAM axis in promoting alveolar cell plasticity, beyond cell proliferation control, proposing a potential therapeutic avenue for lung fibrosis prevention.

Nature CommunicationsVol. 15(1)
Boston Children's Hospital (US), The University of Texas MD Anderson Cancer Center (US), University of Virginia (US)
Cancer Prevention and Research Institute of Texas, National Institutes of Health, University of Texas MD Anderson Cancer Center, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 3%
Neonatal Respiratory Health Research
6.70
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