首页> 外文期刊>Cellular & molecular biology letters. >A simple and effective protocol for fast isolation of human Tenon’s fibroblasts from a single trabeculectomy biopsy – a comparison of cell behaviour in different culture media
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A simple and effective protocol for fast isolation of human Tenon’s fibroblasts from a single trabeculectomy biopsy – a comparison of cell behaviour in different culture media

机译:一种简单有效的方案,可从单个小梁切除术活检中快速分离出人的Tenon成纤维细胞-比较不同培养基中的细胞行为

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Human Tenon’s fibroblasts (HTFs) play a crucial role in wound healing. They cause postoperative scarring of the filtering bleb and are thus responsible for trabeculectomy failure. This study aimed to find an effective and fast protocol for HTF isolation from trabeculectomy biopsies. The protocol was compared with the commonly recommended HTF isolation procedure, which uses Dulbecco’s modified Eagle’s medium (DMEM). We used Eagle’s minimum essential medium (EMEM) enriched with fibroblast growth factor (FGF), which selectively promoted the proliferation of HTF cells. A secondary goal was to compare HTF morphology, metabolism and growth during parallel cultivation of the isolated cells in FGF-enriched EMEM and DMEM. Standard procedures for HTF isolation from tissue biopsies require a 20- to 30-day culture of the explants to obtain the first monolayer. Our protocol yielded the first monolayer after approx. 15 days. More importantly, the majority of the cells were fibroblasts with only individual epithelium-derived cells present. Using FGF-enriched EMEM allowed 1.3 × 106 vimentin-positive fibroblasts to be obtained from a single biopsy within approx. 25 days. Using DMEM resulted in isolation failure and required exchange to FGF-enriched medium to recover the fibroblast culture. HTFs maintained in FGF-enriched EMEM also showed faster proliferation and a different type I collagen production ability compared to HTFs cultured in DMEM. Thus, FGF-enriched EMEM is recommended for fast propagation of HTFs unless the aim of the study is to assess the effect of a tested agent on proliferation ability or type I collagen production. Our fast protocol for HTF isolation allows easy setup of cell banks by researchers under laboratory conditions and could be very useful during testing of novel ophthalmologic anti-fibrotic agents in vitro. Molecular analysis of HTFs isolated from patients with known treatment histories may provide valuable information on the effects of some medications taken before glaucoma surgery on the subsequent wound-healing process and potential for trabeculectomy failure.
机译:人腱的成纤维细胞(HTF)在伤口愈合中起着至关重要的作用。它们引起术后滤过泡瘢痕形成,因此导致小梁切除术失败。这项研究旨在找到一种有效,快速的从小梁切除术活检中分离HTF的方案。将该协议与常用的HTF隔离程序进行了比较,该程序使用了Dulbecco的改良版Eagle介质(DMEM)。我们使用了富含成纤维细胞生长因子(FGF)的Eagle基本必需培养基(EMEM),该培养基选择性地促进了HTF细胞的增殖。第二个目标是比较分离的细胞在富含FGF的EMEM和DMEM中平行培养期间的HTF形态,代谢和生长。从组织活检中分离HTF的标准程序要求外植体培养20到30天才能获得第一个单层。我们的协议产生了大约第一个单层。 15天。更重要的是,大多数细胞是成纤维细胞,仅存在单个上皮来源的细胞。使用富含FGF的EMEM,可在约1个活检过程中通过一次活检获得1.3×106波形蛋白阳性的成纤维细胞。 25天使用DMEM导致分离失败,需要交换至富含FGF的培养基以恢复成纤维细胞培养物。与在DMEM中培养的HTF相比,在富含FGF的EMEM中维持的HTF也显示出更快的增殖和不同的I型胶原产生能力。因此,除非研究的目的是评估被测药物对增殖能力或I型胶原产生的作用,否则建议将富含FGF的EMEM用于HTF的快速繁殖。我们用于HTF分离的快速方案使研究人员可以在实验室条件下轻松建立细胞库,并且在体外测试新型眼科抗纤维化剂中可能非常有用。从具有已知治疗史的患者中分离出的HTF的分子分析可提供有关在青光眼手术前服用某些药物对后续伤口愈合过程的影响以及小梁切除术失败的可能性的有价值的信息。

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