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一种从单次小梁切除术活检中快速分离人眼球筋膜成纤维细胞的简单有效方法——不同培养基中细胞行为的比较

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.

作者信息

Przekora Agata, Zarnowski Tomasz, Ginalska Grazyna

机构信息

Department of Biochemistry and Biotechnology, Medical University of Lublin, Chodzki 1 Street, 20-093 Lublin, Poland.

Department of Ophthalmology, Medical University of Lublin, Chmielna 1 Street, 20-079 Lublin, Poland.

出版信息

Cell Mol Biol Lett. 2017 Mar 9;22:5. doi: 10.1186/s11658-017-0034-4. eCollection 2017.

Abstract

BACKGROUND

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.

RESULTS

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 × 10 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.

CONCLUSIONS

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.

摘要

背景

人Tenon囊成纤维细胞(HTFs)在伤口愈合中起关键作用。它们会导致滤过泡术后瘢痕形成,从而导致小梁切除术失败。本研究旨在找到一种从小梁切除术活检组织中有效且快速分离HTF的方法。将该方法与常用的推荐HTF分离程序进行比较,后者使用杜尔贝科改良的 Eagle 培养基(DMEM)。我们使用富含成纤维细胞生长因子(FGF)的 Eagle 最低必需培养基(EMEM),其可选择性促进HTF细胞增殖。第二个目标是比较在富含FGF的EMEM和DMEM中平行培养分离细胞期间HTF的形态、代谢和生长情况。

结果

从组织活检中分离HTF的标准程序需要对外植体进行20至30天的培养以获得第一个单层细胞。我们的方法在约15天后产生了第一个单层细胞。更重要的是,大多数细胞是成纤维细胞,仅存在个别上皮来源的细胞。使用富含FGF的EMEM,在约25天内可从单个活检组织中获得1.3×10个波形蛋白阳性成纤维细胞。使用DMEM导致分离失败,需要更换为富含FGF的培养基以恢复成纤维细胞培养。与在DMEM中培养的HTFs相比,在富含FGF的EMEM中培养的HTFs也显示出更快的增殖和不同的I型胶原蛋白产生能力。因此,除非研究目的是评估受试药物对增殖能力或I型胶原蛋白产生的影响,否则推荐使用富含FGF的EMEM进行HTFs的快速增殖。

结论

我们快速分离HTF的方法使研究人员能够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药物期间可能非常有用。对有已知治疗史的患者分离的HTFs进行分子分析,可能会提供有关青光眼手术前服用的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可能性的有价值信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/5415760/f494e77ba6b0/11658_2017_34_Fig1_HTML.jpg

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