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用自体成纤维细胞预种植可改善戊二醛固定的猪主动脉瓣的内皮化。

Preseeding with autologous fibroblasts improves endothelialization of glutaraldehyde-fixed porcine aortic valves.

作者信息

Gulbins Helmut, Goldemund Angelika, Anderson Ingrid, Haas Ulrike, Uhlig Antje, Meiser Bruno, Reichart Bruno

机构信息

Department of Cardiac Surgery, University Hospital Grosshadern, Munich, Germany.

出版信息

J Thorac Cardiovasc Surg. 2003 Mar;125(3):592-601. doi: 10.1067/mtc.2003.48.

Abstract

OBJECTIVE

This study represents the development of a treatment and seeding procedure to improve endothelial cellular adhesion on glutaraldehyde-fixed valves.

METHODS

Porcine aortic valves were fixed with 0.2% glutaraldehyde. Wall pieces of these valves had either no additional treatment (n = 4), incubation in M199 Earle (1x), with sodium carbonate at 2.2 g/L without l-glutamine for 24 hours (n = 4), or additional pretreatment with 5%, 10%, or 15% citric acid (three groups, n = 4 each). Thereafter the pieces were washed and buffered to a physiologic pH. This was followed by seeding of human endothelial cells (5 x 10(6) cells). On the basis of the results of these pilot tests, complete glutaraldehyde-fixed aortic roots treated with 10% citric acid were subjected to cell seeding. The valves were seeded with endothelial cells (4.3 x 10(6) cells) either alone (n = 4) or in combination with preseeding of autologous fibroblasts (2.4 x 10(7) cells, n = 4). After each seeding procedure specimens of the free wall of the grafts were taken. In addition, one leaflet was taken for histologic examination after endothelial cell seeding, after 7 days, and after 21 days. Finally, two commercially available stentless aortic valve prostheses (Freestyle; Medtronic, Inc, Minneapolis, Minn) were treated with 10% citric acid and seeded with human fibroblasts and endothelial cells. Specimen were taken according to the glutaraldehyde-fixed aortic roots. Specimen of all experiments were examined with scanning electron microscopy. Frozen sections were stained immunohistochemically for collagen IV, factor VIII, and CD31.

RESULTS

On untreated glutaraldehyde-fixed aortic wall pieces, only poor adhesion (24%) was seen. No viable cells were found after 1 week. Cellular adhesion was best on aortic wall pieces pretreated with 10% citric acid. After 7 days, the cells formed a confluent layer. Endothelial cell seeding on citric acid-treated complete aortic valves showed 45% adhesion, but no confluent layer was found after 1 week. Preseeding of these valves with autologous fibroblasts resulted in an endothelial cellular adhesion of 76% and a confluent endothelial cell layer after 7 days. The layer remained stable for at least 21 days. Results of staining for collagen IV, factor VIII, and CD31 were positive on the luminal side of these valves, indicating the synthesis of matrix proteins and viability of the cells. Pretreatment of commercially available porcine valves with 10% citric acid and preseeding with autologous fibroblasts followed by endothelial cell seeding resulted in an adhesion of 78%. The cells formed a confluent cell layer after 7 days.

CONCLUSIONS

Pretreatment of glutaraldehyde-fixed porcine aortic valves with citric acid established a surface more suitable for cellular attachment. Preseeding these valves with autologous fibroblasts resulted in a confluent endothelial cell layer on the luminal surface. Flow tests and animal experiments are necessary for further assessment of durability and shear stress resistance.

摘要

目的

本研究旨在开发一种处理和接种程序,以改善内皮细胞在戊二醛固定瓣膜上的黏附。

方法

用0.2%戊二醛固定猪主动脉瓣膜。这些瓣膜的壁片要么不进行额外处理(n = 4),要么在含有2.2 g/L碳酸钠且不含L-谷氨酰胺的M199 Earle(1倍)中孵育24小时(n = 4),要么用5%、10%或15%柠檬酸进行额外预处理(三组,每组n = 4)。此后,将壁片冲洗并缓冲至生理pH值。接着接种人内皮细胞(5×10⁶个细胞)。基于这些预试验结果,用10%柠檬酸处理的完整戊二醛固定主动脉根部进行细胞接种。瓣膜单独接种内皮细胞(4.3×10⁶个细胞)(n = 4)或与自体成纤维细胞预接种(2.4×10⁷个细胞,n = 4)。每次接种程序后,取移植物游离壁的标本。此外,在内皮细胞接种后、7天和21天后各取一片瓣叶进行组织学检查。最后,用10%柠檬酸处理两个市售的无支架主动脉瓣膜假体(Freestyle;美敦力公司,明尼阿波利斯,明尼苏达州),并接种人成纤维细胞和内皮细胞。根据戊二醛固定主动脉根部的情况取标本。所有实验的标本均用扫描电子显微镜检查。冰冻切片用免疫组织化学法检测IV型胶原、因子VIII和CD31。

结果

在未处理的戊二醛固定主动脉壁片上,仅观察到较差的黏附(24%)。1周后未发现存活细胞。在用10%柠檬酸预处理的主动脉壁片上细胞黏附最佳。7天后,细胞形成汇合层。在柠檬酸处理的完整主动脉瓣膜上接种内皮细胞显示黏附率为45%,但1周后未发现汇合层。这些瓣膜预接种自体成纤维细胞后,内皮细胞黏附率为76%,7天后形成汇合的内皮细胞层。该层至少稳定21天。这些瓣膜腔面的IV型胶原、因子VIII和CD31染色结果为阳性,表明基质蛋白的合成及细胞的存活能力。用10%柠檬酸预处理市售猪瓣膜,预接种自体成纤维细胞后再接种内皮细胞,黏附率为78%。7天后细胞形成汇合细胞层。

结论

用柠檬酸预处理戊二醛固定的猪主动脉瓣膜可建立更适合细胞附着的表面。这些瓣膜预接种自体成纤维细胞可在腔面形成汇合的内皮细胞层。进一步评估耐久性和抗剪切应力需要进行血流测试和动物实验。

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