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β-Catenin/Lin28/let-7 regulatory network determines type II alveolar epithelial stem cell differentiation phenotypes following thoracic irradiation.
- Source :
-
Journal of radiation research [J Radiat Res] 2021 Jan 01; Vol. 62 (1), pp. 119-132. - Publication Year :
- 2021
-
Abstract
- The contribution of type II alveolar epithelial stem cells (AEC II) to radiation-induced lung fibrosis (RILF) is largely unknown. Cell differentiation phenotypes are determined by the balance between Lin28 and lethal-7 microRNA (let-7 miRNA). Lin28 is activated by β-catenin. The aim of this study was to track AEC II phenotypes at different phases of injury following thoracic irradiation and examine the expression of β-catenin, Lin28 and let-7 to identify their role in AEC II differentiation. Results showed that coexpression of prosurfactant protein C (proSP-C, an AEC II biomarker) and HOPX (homeobox only protein X, an AEC I biomarker) or vimentin (a differentiation marker) was detected in AEC II post-irradiation. The protein expression levels of HOPX and proSP-C were significantly downregulated, but vimentin was significantly upregulated following irradiation. The expression of E-cadherin, which prevents β-catenin from translocating to the nucleus, was downregulated, and the expression of β-catenin and Lin28 was upregulated after irradiation (P < 0.05 to P < 0.001). Four let-7 miRNA members (a, b, c and d) were upregulated in irradiated lungs (P < 0.05 to P < 0.001), but let-7d was significantly downregulated at 5 and 6 months (P < 0.001). The ratios of Lin28 to four let-7 members were low during the early phase of injury and were slightly higher after 2 months. Intriguingly, the Lin28/let-7d ratio was strikingly increased after 4 months. We concluded that β-catenin contributed to RILF by promoting Lin28 expression, which increased the number of AEC II and the transcription of profibrotic molecules. In this study, the downregulation of let-7d miRNA by Lin28 resulted in the inability of AEC II to differentiate into type I alveolar epithelial cells (AEC I).<br /> (© The Author(s) 2020. Published by Oxford University Press on behalf of The Japanese Radiation Research Society and Japanese Society for Radiation Oncology.)
- Subjects :
- Alveolar Epithelial Cells radiation effects
Animals
Biomarkers metabolism
Female
Gene Expression Regulation radiation effects
Homeodomain Proteins metabolism
Lung pathology
Mice, Inbred C57BL
MicroRNAs genetics
Phenotype
Pulmonary Surfactant-Associated Protein C metabolism
Stem Cells radiation effects
Vimentin metabolism
X-Rays
Mice
Alveolar Epithelial Cells metabolism
Gene Regulatory Networks radiation effects
MicroRNAs metabolism
RNA-Binding Proteins metabolism
Stem Cells metabolism
Thorax radiation effects
beta Catenin metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1349-9157
- Volume :
- 62
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of radiation research
- Publication Type :
- Academic Journal
- Accession number :
- 33302295
- Full Text :
- https://doi.org/10.1093/jrr/rraa119