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用于子宫内脊柱裂修复的胎儿软骨生物工程。

Bio-engineering of fetal cartilage for in utero spina bifida repair.

作者信息

Dasargyri Athanasia, Reichmann Ernst, Moehrlen Ueli

机构信息

Tissue Biology Research Unit, Department of Surgery, University Children's Hospital Zurich, Zurich, Switzerland.

Pediatric Surgery, University Children's Hospital Zurich, Steinwiesstrasse 75, 8032, Zurich, Switzerland.

出版信息

Pediatr Surg Int. 2020 Jan;36(1):25-31. doi: 10.1007/s00383-019-04573-3. Epub 2019 Oct 1.

Abstract

PURPOSE

During in utero surgical spina bifida repair, a multi-layer closure is used to cover the defect. These soft tissues, however, might be not sufficient to protect the spinal cord during the future life. Our goal is to develop a more rigid protective tissue construct consisting of bioengineered cartilage and skin.

METHODS

Ovine fetal chondrocytes were tested for their in vitro chondrogenic potential in three-dimensional cultures. Scaffolds based on natural biopolymers (collagen I, fibrin glue) were loaded with varying amounts of fetal chondrocytes and assessed for their ability to support cartilage formation in vitro. The bioengineered constructs were analyzed using cartilage-specific histology stainings and compared to native fetal cartilage.

RESULTS

Fetal chondrocytes actively produced cartilage extracellular matrix in three-dimensional cultures, even at high passages. Among all bioengineered scaffolds, only the collagen I-based hydrogels loaded with high densities of fetal chondrocytes showed cartilage-like structure in vitro but also extensive shrinking.

CONCLUSION

Fetal chondrocytes represent a good cell source for cartilage bioengineering. Collagen I scaffolds support cartilage formation in vitro, but the construct shrinking constitutes a major limitation. Future steps include the identification of suitable bioprintable materials which maintain their shape and size, as well as the analysis of the interphase between bioengineered cartilage and skin.

摘要

目的

在子宫内脊柱裂修复手术中,采用多层缝合来覆盖缺损。然而,这些软组织在未来生活中可能不足以保护脊髓。我们的目标是开发一种由生物工程软骨和皮肤组成的更坚硬的保护性组织构建体。

方法

检测绵羊胎儿软骨细胞在三维培养中的体外软骨形成潜能。基于天然生物聚合物(I型胶原、纤维蛋白胶)的支架负载不同数量的胎儿软骨细胞,并评估其在体外支持软骨形成的能力。使用软骨特异性组织学染色分析生物工程构建体,并与天然胎儿软骨进行比较。

结果

胎儿软骨细胞即使在传代次数较高时,仍能在三维培养中积极产生软骨细胞外基质。在所有生物工程支架中,只有负载高密度胎儿软骨细胞的I型胶原水凝胶在体外显示出软骨样结构,但也有广泛的收缩。

结论

胎儿软骨细胞是软骨生物工程的良好细胞来源。I型胶原支架在体外支持软骨形成,但构建体收缩是一个主要限制。未来的步骤包括鉴定能保持其形状和大小的合适生物可打印材料,以及分析生物工程软骨与皮肤之间的界面。

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