miR-375 regulates rat alveolar epithelial cell trans-differentiation by inhibiting Wnt/-catenin pathway

Author: Wang Yang   Huang Chaoqun   Reddy Chintagari Narendranath   Bhaskaran Manoj   Weng Tingting   Guo Yujie   Xiao Xiao   Liu Lin  

Publisher: Oxford University Press

ISSN: 1362-4962

Source: Nucleic Acids Research, Vol.41, Iss.6, 2013-04, pp. : 3833-3844

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Alveolar epithelial cell (AEC) trans-differentiation is a process where type II alveolar epithelial cells (AEC II) trans-differentiate into type I alveolar epithelial cells (AEC I) during lung recovery after various injuries, in which AEC I are damaged. This process is critical for lung tissue repair. MicroRNAs are a group of small RNAs that regulate gene expression at the post-transcriptional level. They have the potential to regulate almost every aspect of cell physiology. However, whether AEC trans-differentiation is regulated by microRNAs is completely unknown. In this study, we found that miR-375 was downregulated during AEC trans-differentiation. The overexpression of miR-375 with an adenoviral vector inhibited alveolar epithelial trans-differentiation as indicated by an increase in the AEC II marker, surfactant protein C, and decreases in the AEC I markers, T1 and advanced glycosylation end product-specific receptor. miR-375 also inhibited the Wnt/-catenin pathway. The constitutively activation of Wnt/-catenin signaling with a stabilized form of -catenin blocked the miR-375 effects. Frizzled 8 was identified as a target of miR-375. In summary, our results demonstrate that miR-375 regulates AEC trans-differentiation through the Wnt/-catenin pathway. This discovery may provide new targets for therapeutic intervention to benefit lung recovery from injuries.

Related content