首页> 外文期刊>Investigative ophthalmology & visual science >Evaluation of Decellularized Porcine Jejunum as a Matrix for Lacrimal Gland Reconstruction In Vitro for Treatment of Dry Eye Syndrome
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Evaluation of Decellularized Porcine Jejunum as a Matrix for Lacrimal Gland Reconstruction In Vitro for Treatment of Dry Eye Syndrome

机译:脱细胞猪空肠作为体外泪腺重建基质治疗干眼症的评价

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Purpose: Dry eye syndrome (DES) can cause blindness in severe cases, but mainly palliative treatments exist. A tissue-engineered lacrimal gland (LG) could provide a curative treatment. We aimed to evaluate decellularized porcine jejunum (SIS-Muc) as a scaffold for porcine LG epithelial cells. Methods: To evaluate SIS-Muc as a potential scaffold, basement membrane proteins in SIS-Muc and native LG were compared (immunohistochemistry [IHC]). Porcine LG epithelial cells cultured on plastic were characterized (immunocytochemistry), and their culture supernatant was compared with porcine tears (proteomics). Epithelial cells were then seeded onto SIS-Muc in either a static (cell crown) or dynamic culture (within a perfusion chamber) and metabolic (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) and secretory capacities (?2-hexosaminidase assay), protein expression (IHC), and ultrastructure transmission electron microscopy (TEM) compared in each. Results: Collagen IV and laminin were found in both native LG and SIS-Muc. When cultured on plastic, LG epithelial cells expressed pan-cytokeratin, Rab3D, HexA, and produced mucins, but lysozyme and lactoferrin expression was nearly absent. Some porcine tear proteins (lipocalin-2 and lactoferrin) were found in LG epithelial cell culture supernatants. When LG cells were cultured on SIS-Muc, metabolic and ?2-hexosaminidase activities were greater in dynamic cultures than static cultures (P 0.05). In both static and dynamic cultures, cells expressed pan-cytokeratin, Rab3D, lysozyme, and lactoferrin and produced mucins, and TEM revealed cell polarization at the apical surface and cella??cell and cella??scaffold contacts. Conclusions: SIS-Muc is a suitable scaffold for LG cell expansion and may be useful toward reconstruction of LG tissue to provide a curative treatment for DES. Dynamic culture enhances cell metabolic and functional activities.
机译:目的:在严重情况下,干眼症(DES)可能导致失明,但主要存在姑息治疗。组织工程泪腺(LG)可以提供治愈性治疗。我们旨在评估脱细胞的猪空肠(SIS-Muc)作为猪LG上皮细胞的支架。方法:为了评估SIS-Muc作为潜在的支架,比较了SIS-Muc和天然LG中的基底膜蛋白(免疫组化[IHC])。表征在塑料上培养的猪LG上皮细胞(免疫细胞化学),并将其培养上清液与猪眼泪(蛋白质组学)进行比较。然后将上皮细胞以静态(细胞冠)或动态培养(在灌注室内)和代谢(3- [4,5-二甲基噻唑-2-基] -2,5-二苯基四唑鎓)接种到SIS-Muc上并分别比较了它们的分泌能力(β2-己糖胺酶测定),蛋白质表达(IHC)和超微结构透射电子显微镜(TEM)。结果:天然LG和SIS-Muc中均发现了IV型胶原和层粘连蛋白。在塑料上培养时,LG上皮细胞表达泛细胞角蛋白,Rab3D,HexA,并产生粘蛋白,但几乎没有溶菌酶和乳铁蛋白的表达。 LG上皮细胞培养上清液中发现了一些猪眼泪蛋白(lipocalin-2和乳铁蛋白)。当在SIS-Muc上培养LG细胞时,动态培养的代谢和β2-己糖胺酶活性要比静态培养的高(P <0.05)。在静态和动态培养中,细胞均表达泛细胞角蛋白,Rab3D,溶菌酶和乳铁蛋白,并产生粘蛋白,而TEM显示出在顶表面以及细胞与细胞,细胞和细胞与细胞的接触。结论:SIS-Muc是适合LG细胞扩增的支架,可能有助于LG组织的重建,为DES提供治疗。动态培养可增强细胞代谢和功能活性。

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