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人脱细胞羊膜的制备及其细胞相容性和生物相容性

[Preparation of human acellular amniotic membrane and its cytocompatibility and biocompatibility].

作者信息

Luo Jing-cong, Li Xiu-qun, Yang Zhi-ming

机构信息

Division of Stem Cell and Tissue Engineering, Key Laboratory of Biotherapy of Human Diseases Ministry of Education, West China Hospital, Sichuan University, Chengdu, Sichuan, P. R. China 610041.

出版信息

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2004 Mar;18(2):108-11.

Abstract

OBJECTIVE

To prepare human acellular amniotic membrane (HAAM) and to measure its cytocompatibility and biocompatibility.

METHODS

HAAM were prepared by chemical detergent-enzymatic extraction. Fresh human amnion was crosslinked with glutaradehyde, shaken in 0.5% SDS for 24 hours, and then treated with 0.25% trypsin for 4 hours. The production were freeze-drying and sterilized using ethylene oxide. Human fibroblasts were isolated from embryo and expanded in vitro. The fibroblasts were seeded in HAAM. HAAM and specimen were stained with HE and Mallory, and observed grossly, under light microscopy and scanning electron microscopy. The HAAM were implanted in the back of SD rats.

RESULTS

There were no residues of cells in the HAAM (HE, Mallory staining). One side of HAAM had reticular and porous structure, the other side had compact fibrous structure. Pore size was from 10 to 80 nm. The HAAM could be seeded with expanded fibroblasts in vitro, and fibroblasts had the potential of spread and proliferation. The SD rat in the implant test had no death, convulsions and other abnormal response.

CONCLUSION

The detergent-enzymatic extraction process can remove cells and solvable components effectively and preserve the tissue matrix well and keep the reticular structure. The HAAM can be used as an ideal scaffold of biological membrane for tissue engineering.

摘要

目的

制备人脱细胞羊膜(HAAM),并检测其细胞相容性和生物相容性。

方法

采用化学去污剂 - 酶法提取制备HAAM。将新鲜人羊膜用戊二醛交联,在0.5%十二烷基硫酸钠(SDS)中振荡24小时,然后用0.25%胰蛋白酶处理4小时。产物经冷冻干燥并用环氧乙烷灭菌。从胚胎中分离人成纤维细胞并在体外扩增。将成纤维细胞接种于HAAM上。HAAM和标本用苏木精 - 伊红(HE)和马洛里(Mallory)染色,进行大体观察、光学显微镜观察和扫描电子显微镜观察。将HAAM植入SD大鼠背部。

结果

HAAM中无细胞残留(HE、Mallory染色)。HAAM一侧具有网状和多孔结构,另一侧具有致密纤维结构。孔径为10至80纳米。HAAM可在体外接种扩增的成纤维细胞,且成纤维细胞有扩散和增殖的潜能。植入试验中的SD大鼠无死亡、惊厥及其他异常反应。

结论

去污剂 - 酶法提取工艺能有效去除细胞和可溶成分,较好地保留组织基质并保持网状结构。HAAM可作为组织工程理想的生物膜支架。

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