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在兔模型中使用灌注脱细胞技术和间充质干细胞构建组织工程化喉。

Tissue-engineered larynx using perfusion-decellularized technique and mesenchymal stem cells in a rabbit model.

作者信息

Hou Nan, Cui Pengcheng, Luo Jiasheng, Ma Ruina, Zhu Li

机构信息

Department of Otorhinolaryngology Head and Neck Surgery, First Affiliated Hospital, Chengdu Medical College, Sichuan Province, PR China.

出版信息

Acta Otolaryngol. 2011 Jun;131(6):645-52. doi: 10.3109/00016489.2010.547517. Epub 2011 Feb 18.

Abstract

CONCLUSION

Reseeding mesenchymal stem cells (MSCs) into the decellularized laryngeal muscle matrix for construction of a tissue-engineered larynx is feasible. This in vivo maturation in the omentum could be the first step before in situ implantation of the construct. This construct could facilitate a tissue-engineered method for laryngeal reconstruction.

OBJECTIVES

The extracellular matrix (ECM) and MSCs have been widely used for organ reconstruction. Our study aimed to prepare a soft tissue decellularized laryngeal scaffold with intact laryngeal cartilages utilizing a perfusion-decellularized technique, reseeding cells on it, and then construct a recellularized larynx.

METHODS

Perfusion-decellularized larynges were obtained from 20 rabbits by perfusion of the common carotid arteries with detergents. Twelve perfused larynges were observed by macroscopic visualization, histological examination, scanning electron microscopy (SEM), and cartilage viability. The remaining eight perfusion constructs were reseeded with induced MSCs aspirated from eight receptor rabbits. Composites were transferred into greater omentums of receptor rabbits after adherence for 1 day in vitro. Rabbit larynges were harvested after 4 weeks and 8 weeks, respectively. Macroscopic visualization, histological examination, and immunohistochemistry were performed.

RESULTS

Larynges perfused by sodium dodecyl sulfate became transparent after 2 h of perfusion. Histology and SEM indicated that the perfusion method showed a better decullularized effect. Almost no intact cells or nuclei were found, while more pores and collagen fibers were retained in the decellularized matrix. The chondrocyte vitality assay indicated that chondrocyte vitality was high. Vascularization was clearly seen by 4 weeks and relatively integrated cartilage frameworks remained by 8 weeks. Histological and immunohistochemical examinations clearly showed muscle bundles and vessels.

摘要

结论

将间充质干细胞(MSCs)重新接种到脱细胞喉肌基质中构建组织工程化喉是可行的。在大网膜中的这种体内成熟可能是该构建体原位植入前的第一步。这种构建体可为喉重建提供一种组织工程方法。

目的

细胞外基质(ECM)和间充质干细胞已广泛用于器官重建。我们的研究旨在利用灌注脱细胞技术制备具有完整喉软骨的软组织脱细胞喉支架,在其上重新接种细胞,然后构建再细胞化喉。

方法

通过用去污剂灌注颈总动脉从20只兔子获取灌注脱细胞喉。通过宏观观察、组织学检查、扫描电子显微镜(SEM)和软骨活力观察12个灌注喉。将其余8个灌注构建体用从8只受体兔子吸出的诱导间充质干细胞重新接种。体外粘附1天后将复合物转移到受体兔子的大网膜中。分别在4周和8周后收获兔子的喉。进行宏观观察、组织学检查和免疫组织化学检查。

结果

用十二烷基硫酸钠灌注的喉在灌注2小时后变得透明。组织学和SEM表明灌注方法显示出更好的脱细胞效果。几乎未发现完整的细胞或细胞核,而在脱细胞基质中保留了更多的孔隙和胶原纤维。软骨细胞活力测定表明软骨细胞活力高。4周时可见明显的血管化,8周时保留相对完整的软骨框架。组织学和免疫组织化学检查清楚地显示出肌束和血管。

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