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Ultraviolet Irradiation-Induced Volume Alteration of Corneal Epithelial Cells

机译:紫外线诱导角膜上皮细胞的体积变化

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Purpose: The purpose of the study is to understand how extracellular stresses, such as ultraviolet (UV) irradiation, affect corneal epithelial cells. Cell volume changes, damage to corneal epithelial integrity, and cellular responses were assessed after exposure to UVC stresses. Methods: Primary human and rabbit corneal epithelial cells were exposed to UVC light in culture conditions. Ultraviolet C irradiationa??induced changes in cell size and volume were measured by real-time microscopy and self-quenching of the fluorescent dye calcein, respectively. The effects of UVC irradiation on Src and focal adhesion kinase (FAK) phosphorylation and FAK-dependent integrin signaling were detected by ELISA, immunoblotting, and immunostaining. Results: Ultraviolet C irradiation induced both size and volume shifts in human and rabbit corneal epithelial cells. Ultraviolet C irradiation-induced decrease of cell volume elicited activation of Src and FAK, characterized by increased phosphorylations of SrcY416, FAKY397, and FAKY925. In addition, immunostaining studies showed UVC irradiationa??induced increases in phosphorylation of FAK and formation of integrin ?25 clustering. Application of Kv channel blockers, including 4-aminopyridine (4-AP), ?±-DTX, and depressing substance-1 (BDS-1), effectively suppressed UVC irradiationa??induced cell volume changes, and subsequently inhibited UVC irradiationa??induced phosphorylation of Src/FAK, and formation of integrin ?25 clustering, suggesting UVC irradiationa??induced volume changes and Src/FAK activation. Hyperosmotic pressurea??induced volume decreases were measured in comparison with effects of UVC irradiation on volume and Src/FAK activation. However, Kv channel blocker, 4-AP, had no effect on hyperosmotic pressurea??induced responses. Conclusions: The present study demonstrates that UVC irradiationa??induced decreases in cell volume lead to Src/FAK activation due to a rapid loss of K ions through membrane Kv channels.
机译:目的:该研究的目的是了解细胞外应激,例如紫外线(UV)辐射如何影响角膜上皮细胞。暴露于UVC应力后评估细胞体积变化,对角膜上皮完整性的损害和细胞反应。方法:在培养条件下,将人和兔的角膜上皮细胞暴露于UVC光下。紫外线C照射引起的细胞大小和体积的变化分别通过实时显微镜检查和荧光染料钙黄绿素的自淬灭来测量。通过ELISA,免疫印迹和免疫染色检测UVC辐照对Src和粘着斑激酶(FAK)磷酸化以及FAK依赖性整联蛋白信号转导的影响。结果:紫外线C照射可诱导人和兔角膜上皮细胞的大小和体积变化。紫外线C诱导的细胞体积减少引起Src和FAK的活化,其特征是SrcY416,FAKY397和FAKY925的磷酸化增加。另外,免疫染色研究表明,UVC辐照αβ诱导的FAK的磷酸化增加和整联蛋白α25簇的形成。包括4-氨基吡啶(4-AP),α±-DTX和抑制物质1(BDS-1)在内的Kv通道阻滞剂的应用有效地抑制了UVC辐照a-诱导的细胞体积变化,随后抑制了UVC辐照a-。诱导Src / FAK的磷酸化,并形成整联蛋白α25簇,表明UVC辐照αβ诱导了体积变化和Src / FAK活化。与UVC辐照对体积和Src / FAK活化的影响相比,测量了高渗透压引起的体积减少。然而,Kv通道阻滞剂4-AP对高渗压诱导的反应没有作用。结论:本研究表明,由于通过膜Kv通道迅速失去了K离子,UVC辐射诱导的细胞体积减少导致Src / FAK活化。

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