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厚壁组织的成功去细胞化:强调陷阱及多因素方法的必要性。

Successful decellularization of thick-walled tissue: Highlighting pitfalls and the need for a multifactorial approach.

作者信息

Koenig Fabian, Kilzer Marie, Hagl Christian, Thierfelder Nikolaus

机构信息

Department of Cardiac Surgery, Laboratory for Tissue Engineering, Grosshadern Medical Centre, Ludwig-Maximilians-University, Munich, Germany.

出版信息

Int J Artif Organs. 2019 Jan;42(1):17-24. doi: 10.1177/0391398818805624. Epub 2018 Nov 16.

Abstract

INTRODUCTION

: Decellularization of thick tissue is challenging and varying. Therefore, we tried to establish a multifactorial approach for reliable aortic wall decellularization.

METHODS

: Porcine aortic walls were decellularized according to different procedures. Decellularization was performed for 24 (G1), 48 (G2), and 72 h (G3) with a solution of 0.5% desoxycholate and 0.5% dodecyl sulfate. The procedure was characterized using intermittent washing steps, the inclusion of sonication as well as DNase and α-galactosidase treatment. The decellularization efficiency was measured by the evaluation of 4',6-diamidino-2-phenylindole and hematoxylin and eosin staining and quantitative DNA assays. Pentachrome and picrosirius red staining, scanning electron microscopy as well as glycosaminoglycan assays were performed to evaluate the effect of the procedure on the extracellular matrix.

RESULTS

: 4',6-Diamidino-2-phenylindole and hematoxylin and eosin staining revealed a large amount of remaining nuclei in all groups. However, consecutive DNase treatment had a significant effect. While the remaining DNA was detected in some samples of G1 and G2, samples of G3 were fully decellularized. Glycosaminoglycan content was significantly reduced to 50% after 24 h (G1) but remained constant for G2 and G3. Picrosirius red staining revealed an intact and stable collagen network without any visible defects. Pentachrome staining substantiated these results. Nonetheless, the fiber network remains intact, which could be confirmed by reflection electron microscopy analysis.

CONCLUSION

: In this study, we developed a procedure that grants successful decellularization of porcine aortic wall while maintaining the fibrous microstructure. We highlighted the significant effect of DNase and α-galactosidase treatment. In addition, we could show the need for a multifactorial treatment and comprehensive evaluation protocols for thick tissue decellularization.

摘要

引言

厚组织的去细胞化具有挑战性且存在差异。因此,我们试图建立一种多因素方法来实现可靠的主动脉壁去细胞化。

方法

根据不同程序对猪主动脉壁进行去细胞化处理。使用0.5%脱氧胆酸盐和0.5%十二烷基硫酸盐溶液分别处理24小时(G1组)、48小时(G2组)和72小时(G3组)。该程序的特点包括间歇性洗涤步骤、超声处理以及脱氧核糖核酸酶(DNase)和α-半乳糖苷酶处理。通过4',6-二脒基-2-苯基吲哚(DAPI)染色、苏木精和伊红染色以及DNA定量分析来测定去细胞化效率。进行丽春红和天狼星红染色、扫描电子显微镜检查以及糖胺聚糖分析,以评估该程序对细胞外基质的影响。

结果

DAPI染色、苏木精和伊红染色显示所有组中均残留大量细胞核。然而,连续的DNase处理具有显著效果。虽然在G1组和G2组的一些样本中检测到残留DNA,但G3组的样本实现了完全去细胞化。糖胺聚糖含量在24小时(G1组)后显著降低至50%,但G2组和G3组保持恒定。天狼星红染色显示胶原网络完整且稳定,无任何可见缺陷。丽春红染色证实了这些结果。尽管如此,纤维网络保持完整,这可通过反射电子显微镜分析得到证实。

结论

在本研究中,我们开发了一种程序,可成功实现猪主动脉壁的去细胞化,同时保持纤维微观结构。我们强调了DNase和α-半乳糖苷酶处理的显著效果。此外,我们表明厚组织去细胞化需要多因素处理和综合评估方案。

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