June 2017
Volume 58, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2017
A role for the focal adhesion kinase in TGF-β2 induced cell migration in human lens epithelial cells
Author Affiliations & Notes
  • Jie Liu
    Xi'an jiaotong university, Xi'an, China
  • Jingming Li
    Xi'an jiaotong university, Xi'an, China
  • Dan Xu
    Xi'an jiaotong university, Xi'an, China
  • Yongping Shao
    Xi'an jiaotong university, Xi'an, China
  • Cheng Pei
    Xi'an jiaotong university, Xi'an, China
  • Footnotes
    Commercial Relationships   Jie Liu, None; Jingming Li, None; Dan Xu, None; Yongping Shao, None; Cheng Pei, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2017, Vol.58, 3189. doi:
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    • Get Citation

      Jie Liu, Jingming Li, Dan Xu, Yongping Shao, Cheng Pei; A role for the focal adhesion kinase in TGF-β2 induced cell migration in human lens epithelial cells. Invest. Ophthalmol. Vis. Sci. 2017;58(8):3189.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : The role of activated focal adhesion kinase (FAK) signaling pathway in posterior capsule pacification (PCO) remains unclear. Fibronectin, a component of the extracellular matrix, was previously reported to secrete increasingly induced by transforming growth factor (TGF-β2) and interact with integrins on the cell surface. We tested the hypothesis that FAK plays a role in TGF-β2 induced migration in human lens epithelial cells, which was mediated by fibronectin.

Methods : The HLE-B3 cells, a human lens epithelial cell line, was incubated with TGF-β2 (5ng/ml). The expression of fibronectin , p-FAK and FAK were determined by western-blot analysis and expression of integrin α5β1 on the cell surface were detected by flow cytometry. HLE-B3 cells were seeded on culture surface coated with fibronectin (10μg/ml,50μg/ml), polylysine or collagen. Cell adhesion were quantified by crystal violet staining (0.5%). Cell migration capacity were measured by wound-healing assay and transwell migration assay in presence or absence of a FAK inhibitor, fibronectin RNA interference or RGD, which inhibits interaction of integrin and fibronectin. T-test was used for statistical analysis.

Results : TGF-β2 promoted HLE-B3 cell migration in a dose-dependent manner. TGF-β2 upregulated fibronectin expression (p = 0.007), which was followed by increased phosphorylation of FAK (p = 0.001). Meanwhile, we found that integrin α5β1 was abundantly expressed on cell surface. Disrupting intergrin-fibronection interaction by RGD reduced TGF-β2-induced cell migration. Moreover, cell adhesion (1.50±0.17, p = 0.030), migration (2.25±0.10, p = 0.0007) and p-FAK expression (2.64±0.03, p = 0.0002) were markedly increased on a fibronectin-coated surface compared to polylysine-coated or collagen-coated ones, which was abolished by RGD treatment. Suppression of FAK signaling by its inhibitor or fibronectin SiRNA attenuated TGF-β2-induced HLE-B3 migration (p = 0.0001).

Conclusions : Our results are consistent with our hypothesis that TGF-β2 can induce phosphorylation of FAK and, subsequently, promote cell migration, which was mediated by fibronectin in human lens epithelial cells.

This is an abstract that was submitted for the 2017 ARVO Annual Meeting, held in Baltimore, MD, May 7-11, 2017.

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