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Mycophenolic acid suppresses human pterygium and normal tenon fibroblast proliferation in vitro.

机译:霉酚酸在体外可抑制人翼状and肉和正常肌腱成纤维细胞的增殖。

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AIMS: To investigate whether mycophenolic acid (MPA) exerts antifibrotic effects on pterygium fibroblasts (PFB) with and without stimulation with fibrogenic cytokines, and to compare the efficacy of MPA with mitomycin (MMC) and dexamethasone (DXM) on PFB and tenon fibroblasts (TFB). METHODS: TFB and PFB were obtained from tissue explants during strabismus or pterygium surgery. Proliferation of subconfluent fibroblasts +/- basic fibroblast growth factor (bFGF) (10 ng/ml) was assessed by using the (3H) thymidine-incorporation assay. Cell cultures were incubated with MPA, MMC or DXM. Apoptosis was evaluated by quantifying Annexin V and propidium iodide positive cells with flow cytometry. RESULTS: MPA showed a concentration-dependent inhibition of proliferation of PFB +/- bFGF as well as TFB +/- bFGF. The antiproliferative effect of MPA was comparable with that of MMC and DXM. Short exposure of PFB to MPA under profibrogenic conditions was significantly inhibitory. No apoptotic effect was found on TFB. CONCLUSIONS: MPA suppressed tenon and pterygium fibroblast proliferation in vitro under basal and profibrogenic conditions. It was comparable with MMC under long-term exposure, but MMC was more suppressive under short-term exposure. MPA may be safer than MMC due to a more specific mechanism of action and lack of cytotoxicity. Further investigation is warranted regarding MPA concentrations that will lead to a potent antiproliferative effect in vivo.
机译:目的:研究霉酚酸(MPA)在有或没有刺激成纤维细胞因子的情况下是否对翼状ery肉成纤维细胞(PFB)发挥抗纤维化作用,并比较MPA与丝裂霉素(MMC)和地塞米松(DXM)对PFB和肌腱成纤维细胞的疗效( TFB)。方法:TFB和PFB是在斜视或翼状surgery肉手术中从组织外植体获得的。使用(3H)胸腺嘧啶核苷掺入法评估亚汇合成纤维细胞+/-碱性成纤维细胞生长因子(bFGF)(10 ng / ml)的增殖。细胞培养物与MPA,MMC或DXM孵育。通过用流式细胞仪定量膜联蛋白V和碘化丙啶阳性细胞来评估细胞凋亡。结果:MPA对PFB +/- bFGF和TFB +/- bFGF的增殖都有浓度依赖性的抑制作用。 MPA的抗增殖作用与MMC和DXM相当。在纤维化条件下,PFB短时间暴露于MPA具有明显的抑制作用。在TFB上未发现凋亡作用。结论:MPA在基础和原纤维形成条件下抑制了腱和翼状肉成纤维细胞的增殖。在长期暴露下,它与MMC相当,但在短期暴露下,MMC更具抑制性。由于更具体的作用机制和缺乏细胞毒性,MPA可能比MMC更安全。关于MPA的浓度,将导致体内有效的抗增殖作用,需要做进一步的研究。

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