Literature DB >> 25875044

Combined silencing of TGF-β2 and Snail genes inhibit epithelial-mesenchymal transition of retinal pigment epithelial cells under hypoxia.

Zhuolei Feng1, Ruishu Li, Huanqi Shi, Wenjiao Bi, Wenwen Hou, Xiaomei Zhang.   

Abstract

BACKGROUND: The formation of scar-like fibrous tissue in age-related macular degeneration (AMD) is associated with hypoxia. Under hypoxia, retinal pigment epithelial (RPE) cells can secret more transforming growth factor-β2 (TGF-β2), which is determined to induce epithelial-mesenchymal transition (EMT) at certain concentrations. Whether hypoxia can induce EMT by stimulating RPE cell line secrets TGF-β2 or not remains unknown. To gain a better understanding of the signaling mechanisms of fibrosis in AMD under hypoxic conditions, we investigated EMT in retinal pigment epithelial (RPE) cells and the effect of TGF-β2 and Snail in this process.
METHODS: Human RPE cell line (ARPE-19) was incubated with 5 % O2 for different periods of time. The expression of N-cadherin, α-smooth muscle actin (α-SMA), TGF-β2 , and Snail were determined by Western blot and real-time PCR. Cell proliferation was assessed by CCK8 kit. RNA interference was used for multi-gene silencing of TGF-β2 and Snail genes.
RESULTS: N-cadherin was decreased and mesenchymal cell marker α-SMA was increased after the ARPE-19 cell line was incubated with 5 % O2. Meanwhile, the proliferation capability of the cell line was increased. TGF-β2 and Snail expression were increased in a time-dependent manner under hypoxia. After multi-silencing TGF-β2 and Snail genes, N-cadherin was increased and α-SMA was reduced. Meanwhile, the proliferation of the cell line was suppressed.
CONCLUSIONS: Under hypoxic conditions, RPE cells undergo EMT. Endogenic TGF-β2 and Snail are involved in this process. Furthermore, knockdown of both TGF-β2 and Snail inhibited EMT to a greater extent than knockdown of either gene individually.

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Year:  2015        PMID: 25875044     DOI: 10.1007/s00417-014-2922-x

Source DB:  PubMed          Journal:  Graefes Arch Clin Exp Ophthalmol        ISSN: 0721-832X            Impact factor:   3.117


  43 in total

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