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雷帕霉素靶蛋白抑制剂对小梁切除术后纤维化的影响。

Effects of mammalian target of rapamycin inhibitors on fibrosis after trabeculectomy.

机构信息

Department of Ophthalmology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

Department of Ophthalmology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

出版信息

Exp Eye Res. 2021 Feb;203:108421. doi: 10.1016/j.exer.2020.108421. Epub 2020 Dec 24.

Abstract

Glaucoma, the second leading cause of blindness worldwide, is characterized by aberrant elevations of intraocular pressure (IOP), which can damage the optic nerve. IOP reduction is the only effective therapy for prevention of visual impairment and blindness in both hypertensive and normotensive individuals, and in some cases, trabeculectomy is a major surgical procedure that can lower IOP in patients with glaucoma. No matter how surgical technique and postoperative care advances, excessive scarring and tissue fibrosis could result from increased human conjunctival fibroblast (HCF) proliferation and extracellular matrix (ECM) deposition of the subconjunctival tissue and scleral flaps would persist after trabeculectomy. And these issues are major impediments to IOP reduction and filtering of bleb formations, so the modulation of the factors which can induce fibrosis could used as a novel strategy to control scarring after trabeculectomy. In this study, we examined the effects of mammalian target of rapamycin (mTOR) inhibitors (rapamycin or Torin1) on the fibrotic response induced by transforming growth factor-beta 1 (TGF-β1) in cultured human conjunctival fibroblast (HCF) cells. The study also examined the effects of mTOR inhibitor on fibrosis after trabeculectomy in rabbit eyes. In in vitro studies, we stimulated HCFs with TGF-β1, and confirmed that the expression levels of fibronectin, collagen type I alpha 1 chain (COL1A1), and α-smooth muscle actin (SMA) were significantly upregulated in HCFs with TGF-β1, by means of quantitative real-time polymerase chain reaction and immunocytochemistry. And those TGF-β1-induced changes were significantly attenuated with mTOR inhibitors, rapamycin or Torin1. Additionally the migration rate of HCFs was examined under conditions of TGF-β1 induction, TGF-β1-induced changes were significantly attenuated with mTOR inhibitors. A rabbit model of trabeculectomy was examined in vivo, and the effects of topical mTOR inhibitor were also examined, and found that topical treatment with mTOR inhibitor significantly suppressed collagen deposition in rabbit eyes after trabeculectomy. These results have demonstrated that mTOR inhibitors may provide a novel treatment modality for reducing the fibrotic response in HCFs and improving bleb scarring after filtration surgery.

摘要

青光眼是全球第二大致盲原因,其特征为眼内压(IOP)异常升高,可导致视神经损伤。降低 IOP 是预防高血压和正常血压个体视力损害和失明的唯一有效治疗方法,在某些情况下,小梁切除术是一种主要的手术程序,可降低青光眼患者的 IOP。无论手术技术和术后护理如何进步,人结膜成纤维细胞(HCF)的过度增殖以及结膜下组织和巩膜瓣的细胞外基质(ECM)沉积都会导致过多的瘢痕和组织纤维化,并且在小梁切除术后这些问题仍然存在。这些问题是导致 IOP 降低和滤过泡形成障碍的主要障碍,因此,调节可诱导纤维化的因素可作为控制小梁切除术后瘢痕形成的新策略。在这项研究中,我们研究了哺乳动物雷帕霉素靶蛋白(mTOR)抑制剂(雷帕霉素或 Torin1)对转化生长因子-β1(TGF-β1)诱导的培养人结膜成纤维细胞(HCF)细胞纤维化反应的影响。该研究还研究了 mTOR 抑制剂对兔眼小梁切除术后纤维化的影响。在体外研究中,我们用 TGF-β1 刺激 HCF,通过定量实时聚合酶链反应和免疫细胞化学证实 TGF-β1 可显著上调 HCF 中纤连蛋白、I 型胶原α1 链(COL1A1)和α-平滑肌肌动蛋白(SMA)的表达水平。并且 mTOR 抑制剂可显著减弱 TGF-β1 诱导的这些变化,雷帕霉素或 Torin1。此外,我们还在 TGF-β1 诱导的条件下检测了 HCF 的迁移率,结果发现 mTOR 抑制剂可显著减弱 TGF-β1 诱导的变化。我们在体内建立了兔小梁切除术模型,并研究了局部 mTOR 抑制剂的作用,发现局部应用 mTOR 抑制剂可显著抑制兔眼小梁切除术后的胶原沉积。这些结果表明,mTOR 抑制剂可能为减少 HCF 纤维化反应和改善滤过性手术后的滤过泡瘢痕形成提供一种新的治疗方法。

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