Abidin Fadhilah Z, Gouveia Ricardo M, Connon Che J
a Institute of Genetic Medicine; Newcastle University; Center for Life ; Newcastle , UK.
Organogenesis. 2015;11(3):122-36. doi: 10.1080/15476278.2015.1093267.
Retinoic acid has recently been shown to control the phenotype and extracellular matrix composition of corneal stromal cells cultured in vitro as monolayers. This study set out to investigate the effects of retinoic acid on human corneal keratocytes within a 3D environment. Human corneal keratocytes were encapsulated in collagen gels, which were subsequently compressed under load, and cultured in serum-free media supplemented with 10 µM retinoic acid or DMSO vehicle for 30 days. Cell proliferation was quantified on selected days, while the expression of several important keratocytes markers was evaluated at day 30 using RT-PCR and immunoblotting. The weight and size of the collagen constructs were measured before and after hydration and contraction analyses. Retinoic acid enhanced keratocyte proliferation until day 30, whereas cells in control culture conditions showed reduced numbers after day 21. Both gene and protein expressions of keratocyte-characteristic proteoglycans (keratocan, lumican and decorin), corneal crystallins and collagen type I and V were significantly increased following retinoic acid supplementation. Retinoic acid also significantly reduced the expression of matrix metalloproteases 1, 3 and 9 while not increasing α-smooth muscle actin and fibronectin expression. Furthermore, these effects were also correlated with the ability of retinoic acid to significantly inhibit the contractility of keratocytes while allowing the build-up of corneal stromal extracellular matrix within the 3D constructs. Thus, retinoic acid supplementation represents a promising strategy to improve the phenotype of 3D-cultured keratocytes, and their usefulness as a model of corneal stroma for corneal biology and regenerative medicine applications.
最近研究表明,视黄酸可控制体外单层培养的角膜基质细胞的表型和细胞外基质组成。本研究旨在探讨视黄酸在三维环境中对人角膜基质细胞的影响。将人角膜基质细胞包裹于胶原凝胶中,随后在负载下进行压缩,并在添加10 µM视黄酸或二甲基亚砜载体的无血清培养基中培养30天。在选定的日子对细胞增殖进行定量,同时在第30天使用逆转录-聚合酶链反应(RT-PCR)和免疫印迹法评估几种重要的角膜基质细胞标志物的表达。在水合和收缩分析前后测量胶原构建体的重量和大小。视黄酸可促进角膜基质细胞增殖直至第30天,而对照培养条件下的细胞在第21天后数量减少。补充视黄酸后,角膜基质细胞特征性蛋白聚糖(角膜蛋白聚糖、亮蛋白聚糖和核心蛋白聚糖)、角膜晶体蛋白以及I型和V型胶原的基因和蛋白表达均显著增加。视黄酸还显著降低基质金属蛋白酶1、3和9的表达,同时不增加α-平滑肌肌动蛋白和纤连蛋白的表达。此外,这些作用还与视黄酸显著抑制角膜基质细胞收缩性、同时允许在三维构建体内积聚角膜基质细胞外基质的能力相关。因此,补充视黄酸是改善三维培养角膜基质细胞表型的一种有前景的策略,并且其作为角膜生物学和再生医学应用的角膜基质模型具有实用性。