Wilson Samantha L, Sidney Laura E, Dunphy Siobhán E, Dua Harminder S, Hopkinson Andrew
a Academic Ophthalmology, Division of Clinical Neuroscience, Queen's Medical Centre Campus, University of Nottingham , Nottingham , UK.
Curr Eye Res. 2016 Jun;41(6):769-82. doi: 10.3109/02713683.2015.1062114. Epub 2015 Sep 23.
There is a clinical need for biomimetic corneas that are as effective, preferably superior, to cadaveric donor tissue. Decellularized tissues are advantageous compared to synthetic or semi-synthetic engineered tissues in that the native matrix ultrastructure and intrinsic biological cues including growth factors, cytokines and glycosaminoglycans may be retained. However, there is currently no reliable, standardized human corneal decellularization protocol.
Corneal eye-bank tissue unsuitable for transplantation was utilized to systematically compare commonly used decellularization protocols. Hypertonic sodium chloride; an ionic reagent, sodium dodecyl sulphate; a non-ionic detergent, tert-octylphenol polyoxyethylene (Triton-X); enzymatic disaggregation using Dispase; mechanical agitation; and the use of nucleases were investigated. Decellularization efficacy, specifically for human corneal tissue, was extensively evaluated. Removal of detectable cellular material was evidenced by histological, immunofluorescence and biochemical assays. Preservation of macroscopic tissue transparency and light transmittance was evaluated. Retention of corneal architecture, collagen and glycosaminoglycans was assessed via histological, immunofluorescence and quantitative analysis. Biocompatibility of the resulting scaffolds was assessed using cell proliferation assays.
None of the decellularization protocols investigated successfully removed 100% of cellular components. The techniques with the least residual cellular material were most structurally compromised. Biochemical analysis of glycosaminoglycans demonstrated the stripping effects of the decellularization procedures.
The ability to utilize, reprocess and regenerate tissues deemed "unsuitable" for transplantation allows us to salvage valuable tissue. Reprocessing the tissue has the potential to have a considerable impact on addressing the problems associated with cadaveric donor shortage. Patients would directly benefit by accessing greater numbers of corneal grafts and health authorities would fulfill their responsibility for the delivery of effective corneal reconstruction to alleviate corneal blindness. However, in order to progress, we may need to take a step back to establish a "decellularization" criterion; which should balance effective removal of immune reactive material with maintenance of tissue functionality.
临床上需要仿生角膜,其效果与尸体供体组织相同,最好优于尸体供体组织。与合成或半合成工程组织相比,脱细胞组织具有优势,因为其可以保留天然基质超微结构以及包括生长因子、细胞因子和糖胺聚糖在内的内在生物学信号。然而,目前尚无可靠、标准化的人角膜脱细胞方案。
利用不适合移植的角膜库组织系统比较常用的脱细胞方案。研究了高渗氯化钠(一种离子试剂)、十二烷基硫酸钠(一种非离子洗涤剂)、叔辛基酚聚氧乙烯(曲拉通-X)、使用Dispase进行酶解、机械搅拌以及使用核酸酶的效果。广泛评估了脱细胞效果,特别是对人角膜组织的脱细胞效果。通过组织学、免疫荧光和生化分析证明可检测细胞物质的去除情况。评估宏观组织透明度和透光率的保留情况。通过组织学、免疫荧光和定量分析评估角膜结构、胶原蛋白和糖胺聚糖的保留情况。使用细胞增殖试验评估所得支架的生物相容性。
所研究的脱细胞方案均未成功去除100%的细胞成分。残留细胞物质最少的技术在结构上受损最大。糖胺聚糖的生化分析证明了脱细胞过程的剥离作用。
利用、再处理和再生被认为“不适合”移植的组织的能力使我们能够挽救有价值的组织。对组织进行再处理有可能对解决与尸体供体短缺相关的问题产生重大影响。患者将直接受益于获得更多的角膜移植,卫生当局将履行其提供有效角膜重建以缓解角膜盲的责任。然而,为了取得进展,我们可能需要退一步建立一个“脱细胞”标准;该标准应在有效去除免疫反应性物质与维持组织功能之间取得平衡。