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冷冻保存对心脏瓣膜小叶细胞外基质结构的影响。

Impact of cryopreservation on extracellular matrix structures of heart valve leaflets.

作者信息

Schenke-Layland Katja, Madershahian Navid, Riemann Iris, Starcher Barry, Halbhuber Karl-Jürgen, König Karsten, Stock Ulrich A

机构信息

Department of Cardiothoracic and Vascular Surgery, Friedrich-Schiller-University, Jena, Germany.

出版信息

Ann Thorac Surg. 2006 Mar;81(3):918-26. doi: 10.1016/j.athoracsur.2005.09.016.

Abstract

BACKGROUND

Transplantation of cryopreserved allografts represents a well-established valve replacement option. Despite their clinical use for more than 40 years, the integrity of the extracellular matrix (ECM) of these valves after thawing has not been determined. The purpose of this study was to investigate and compare ECM structures of fresh and cryopreserved porcine heart valve leaflets with special emphasis on the condition of collagenous and elastic fibers.

METHODS

Pulmonary valves were excised from unprocessed porcine hearts under sterile conditions. After treatment with antibiotics, the valves were incubated in a cryoprotective solution, cryopreserved stepwise, and stored at -196 degrees C for 1 week. Two groups of heart valves (fresh untreated and thawed cryopreserved [each, n = 8]) were analyzed using biochemical (collagen, elastin, desmosine), histologic (hematoxylin-eosin, Movat-pentachrome, resorcin-fuchsin), and immunohistochemical (antibodies against collagen I, III, IV, and elastin) methods. Near-infrared femtosecond multiphoton laser scanning microscopy and second harmonic generation were used for high-resolution three-dimensional imaging of ECM structures.

RESULTS

Biochemical testing demonstrated similar amounts of collagen and desmosine, but a minor loss of elastin in the cryopreserved specimens. Conventional histology revealed almost comparable cell and ECM formations in fresh and cryopreserved valve leaflets. In contrast, laser-induced autofluorescence imaging showed substantial ultrastructural deterioration and disintegration of most collagenous structures. Second harmonic generation was not inducible.

CONCLUSIONS

Conventional cryopreservation of heart valves is accompanied by serious alterations and destruction of leaflet ECM structures, specifically demonstrated by multiphoton imaging. Further in-depth studies to clarify the impact of alternative cryopreservation techniques proposed for clinical use, such as vitrification, are crucial.

摘要

背景

冷冻保存同种异体移植物的移植是一种成熟的瓣膜置换选择。尽管这些瓣膜已临床应用40多年,但解冻后其细胞外基质(ECM)的完整性尚未确定。本研究的目的是调查和比较新鲜和冷冻保存的猪心脏瓣膜小叶的ECM结构,特别关注胶原纤维和弹性纤维的状况。

方法

在无菌条件下从未经处理的猪心脏中取出肺动脉瓣。用抗生素处理后,将瓣膜置于冷冻保护溶液中,逐步冷冻保存,并在-196℃下储存1周。使用生化方法(胶原蛋白、弹性蛋白、锁链素)、组织学方法(苏木精-伊红染色、莫瓦特-五色染色、间苯二酚-品红染色)和免疫组织化学方法(抗I型、III型、IV型胶原蛋白和弹性蛋白抗体)对两组心脏瓣膜(新鲜未处理组和解冻冷冻保存组[每组n = 8])进行分析。使用近红外飞秒多光子激光扫描显微镜和二次谐波产生技术对ECM结构进行高分辨率三维成像。

结果

生化测试表明,冷冻保存标本中的胶原蛋白和锁链素含量相似,但弹性蛋白略有损失。传统组织学显示新鲜和冷冻保存的瓣膜小叶中的细胞和ECM形成几乎相当。相比之下,激光诱导的自发荧光成像显示大多数胶原结构出现严重的超微结构恶化和崩解。无法诱导二次谐波产生。

结论

心脏瓣膜的传统冷冻保存伴随着小叶ECM结构的严重改变和破坏,多光子成像特别显示了这一点。进一步深入研究以阐明临床应用中提出的替代冷冻保存技术(如玻璃化)的影响至关重要。

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