Journal
IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL
Volume 57, Issue 10, Pages 944-952Publisher
SPRINGER
DOI: 10.1007/s11626-021-00607-0
Keywords
Airway smooth muscle (ASM); Hypoxia; Hypoxia-inducible factor-1 alpha (HIF-l alpha); miRNA-103; Phosphatase and tensin homology deleted on chromosome ten (PTEN)
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Funding
- National Natural Science Foundation Project [81901299]
- Natural Science Foundation of Jiangsu Province [SBK2017042600, BK20170255]
- Foundation of Jiangsu Province Six Talents Peak [JY-061]
- Foundation of Key Laboratory of New Drug Research and Clinical Pharmacy of Jiangsu Province [KF-XY201403]
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Our study showed that HIF-1 alpha promotes ASM cell proliferation by upregulating miRNA-103 expression under hypoxia, with PTEN playing a role in the miRNA-103-mediated pathway.
The hypoxia-inducible factor-1 alpha (HIF-1 alpha) activated during asthma development plays a causative role in the abnormal proliferation of airway smooth muscle (ASM) cells and consequential airway remodeling. Although the underlying mechanisms of HIF-1 alpha activity have not been fully revealed, HIF-1 alpha-regulated miRNA signaling is considered important for disrupted differentiation and proliferation of local cells in various tissues under inflammation. We aimed to identify the key miRNA signaling involved in HIF-1 alpha regulation of the proliferation of ASM cells. This study was based on primary ASM cells isolated from adult male rats. Three percent O-2 and 21% O-2 were set as hypoxic and normoxic condition for ASM cell treatment, respectively. Knockdown of HIF-1 alpha was performed through transfection of pSUPER-shHIF-1 alpha plasmid. Overexpression and knockdown of miRNA-103 were performed through transfection of miRNA-103 mimic or inhibitor, respectively. Levels of HIF-l alpha, PTEN, and PCNA were determined with Western blot and RT-qPCR. Hypoxia increased HIF-1 alpha and miRNA-103 expression and proliferation in ASM cells. Knockdown of HIF-1 alpha suppressed hypoxia-induced upregulation of proliferation and miRNA-103 expression in ASM cells. Knockdown of miRNA-103 displayed similar effects as knockdown of HIF-1 alpha in ASM cells under hypoxia, while overexpression of miRNA-103 played the opposite role. Additionally, increased or decreased expression of PTEN was also detected when HIF-1 alpha/miRNA-103 was knocked down under hypoxia or miRNA-103 was overexpressed under normoxia, respectively. Our results suggest that HIF-1 alpha promotes the proliferation of ASM cells via upregulating miRNA-103 expression under hypoxia, and PTEN is involved in the miRNA-103-mediated signaling pathway.
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