<i>miR-29b</i> Regulates TGF-β1-Induced Epithelial–Mesenchymal Transition by Inhibiting Heat Shock Protein 47 Expression in Airway Epithelial Cells

Tissue remodeling contributes to ongoing inflammation and refractoriness of chronic rhinosinusitis (CRS). During this process, epithelial-mesenchymal transition (EMT) plays an important role in dysregulated remodeling and both <i>microRNA (miR)-29b</i> and heat shock protein 47 (HSP47) m...

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Autores principales: Jae-Min Shin, Joo-Hoo Park, Hyun-Woo Yang, Jee Won Moon, Heung-Man Lee, Il-Ho Park
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/19782d895def4032b7cd9359a14060fc
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Sumario:Tissue remodeling contributes to ongoing inflammation and refractoriness of chronic rhinosinusitis (CRS). During this process, epithelial-mesenchymal transition (EMT) plays an important role in dysregulated remodeling and both <i>microRNA (miR)-29b</i> and heat shock protein 47 (HSP47) may be engaged in the pathophysiology of CRS. This study aimed to determine the role of <i>miR-29b</i> and HSP47 in modulating transforming growth factor (TGF)-β1-induced EMT and migration in airway epithelial cells. Expression levels of <i>miR-29b</i>, HSP47, E-cadherin, α-smooth muscle actin (α-SMA), vimentin and fibronectin were assessed through real-time PCR, Western blotting, and immunofluorescence staining. <i>Small interfering RNA</i> (<i>siRNA</i>) targeted against <i>miR-29b</i> and <i>HSP47</i> were transfected to regulate the expression of EMT-related markers. Cell migration was evaluated with wound scratch and transwell migration assay. <i>miR-29b</i> mimic significantly inhibited the expression of HSP47 and TGF-β1-induced EMT-related markers in A549 cells. However, the <i>miR-29b</i> inhibitor more greatly induced the expression of them. HSP47 knockout suppressed TGF-β1-induced EMT marker levels. Functional studies indicated that TGF-β1-induced EMT was regulated by <i>miR-29b</i> and HSP47 in A549 cells. These findings were further verified in primary nasal epithelial cells. <i>miR-29b</i> modulated TGF-β1-induced EMT-related markers and migration via HSP47 expression modulation in A549 and primary nasal epithelial cells. These results suggested the importance of <i>miR-29b</i> and HSP47 in pathologic tissue remodeling progression in CRS.