Stern Irit, Barrera Valentina, Randles Michael, Rooney Paul
NHS Blood and Transplant, Tissue Services, 14 Estuary Banks, Speke, Liverpool, L24 8RB, UK.
NHS Blood and Transplant, Tissue Services R&D, 14 Estuary Banks, Speke, Liverpool, L24 8RB, UK.
Cell Tissue Bank. 2024 Dec 10;26(1):3. doi: 10.1007/s10561-024-10153-0.
Non-healing wounds cost the National Health Service over £5.6 billion annually in wound management. Skin allografts are used to treat non-healing wounds, ulcers and burns, offering the best protection against infection. In order to allow host cells to repopulate and to avoid immunogenicity, cell components are removed through decellularisation. Decellularisation of human dermis has so far been performed in NHS Blood and Transplant using a combination of two enzymes (RNase T1 and the recombinant human DNase Pulmozyme)®. This study aims at validating a new method to remove DNA from donated dermis via the use of a single enzyme, Benzonase, known for its effectiveness of DNA digestion. Skin samples were decellularised by removing the epidermis, lysing of dermal cells, removal of cellular fragments by a detergent wash and removal of nucleic acids by a nuclease incubation with either Benzonase or Pulmozyme + RNase T1. DNA quantification with PicoGreen, as well as histology on wax-embedded biopsies, stained with DAPI and haemotoxylin and eosin, were performed. In vitro toxicity test on human osteosarcoma immortalised cells and skin fibroblasts, and biomechanical (tensile) testing, were also performed. The effectiveness of DNA digestion with the new methodology was comparable to previous procedure. Mean DNA removal percentage following decellularisation with Pulmozyme + RNase was 99.9% (3.83 ng/mg). Mean DNA removal percentage with Benzonase was 99.8% (9.97 ng/mg). Histology staining showed complete decellularisation following either method. Benzonase was proven to be non-toxic to both cell lines used, and a one-way Anova test showed no significant difference in neither stress nor strain between acellular dermal matrix decellularised with either Benzonase or Pulmozyme + RNase T1. Benzonase was able to effectively decellularise dermis after prior removal of epidermis. It performed just as well as the combination of Pulmozyme + RNase T1, but represents significant advantages in terms of cost effectiveness, procurement and storage; Benzonase has been successfully used in the decellularisation of other tissues, thus would be better for Tissue Banking use. Switching to this combined DNase/RNase can have far-reaching consequences in the production of acellular human dermal matrix by NHSBT and in the treatment of patients requiring it.
每年,不愈合伤口的处理给国民医疗服务体系造成的花费超过56亿英镑。皮肤异体移植被用于治疗不愈合伤口、溃疡和烧伤,能提供最佳的抗感染保护。为了让宿主细胞重新生长并避免免疫原性,通过脱细胞处理去除细胞成分。迄今为止,在国民医疗服务体系血液及移植中心,人类真皮的脱细胞处理是使用两种酶(核糖核酸酶T1和重组人脱氧核糖核酸酶勃拉酶)的组合来进行的。本研究旨在验证一种通过使用单一酶——核酸酶,因其消化DNA的有效性而闻名,从捐赠的真皮中去除DNA的新方法。通过去除表皮、裂解真皮细胞、用去污剂洗涤去除细胞碎片以及用核酸酶(核酸酶或勃拉酶+核糖核酸酶T1)孵育去除核酸,对皮肤样本进行脱细胞处理。用PicoGreen进行DNA定量分析,并对石蜡包埋活检组织进行组织学检查,用4',6-二脒基-2-苯基吲哚、苏木精和伊红染色。还对人骨肉瘤永生化细胞和皮肤成纤维细胞进行了体外毒性试验以及生物力学(拉伸)试验。新方法对DNA的消化效果与之前的方法相当。用勃拉酶+核糖核酸酶进行脱细胞处理后,DNA去除率平均为99.9%(3.83纳克/毫克)。用核酸酶处理后,DNA去除率平均为99.8%(9.97纳克/毫克)。组织学染色显示两种方法处理后均实现了完全脱细胞。已证明核酸酶对所使用的两种细胞系均无毒,单向方差分析表明,用核酸酶或勃拉酶+核糖核酸酶T1进行脱细胞处理的无细胞真皮基质在应力和应变方面均无显著差异。在预先去除表皮后,核酸酶能够有效地使真皮脱细胞。其效果与勃拉酶+核糖核酸酶T1的组合相当,但在成本效益、采购和储存方面具有显著优势;核酸酶已成功用于其他组织的脱细胞处理,因此更适合组织库使用。改用这种脱氧核糖核酸酶/核糖核酸酶组合对国民医疗服务体系血液及移植中心生产无细胞人真皮基质以及对需要它的患者的治疗可能会产生深远影响。