首页> 外文期刊>Journal of tissue engineering and regenerative medicine >Fate of bone marrow mesenchymal stem cells following the allogeneic transplantation of cartilaginous aggregates into osteochondral defects of rabbits.
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Fate of bone marrow mesenchymal stem cells following the allogeneic transplantation of cartilaginous aggregates into osteochondral defects of rabbits.

机译:软骨聚集体同种异体移植到兔骨软骨缺损后骨髓间充质干细胞的命运。

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摘要

The purpose of this study was to track mesenchymal stem cells (MSCs) labelled with internalizing quantum dots (i-QDs) in the reparative tissues, following the allogeneic transplantation of three-dimensional (3D) cartilaginous aggregates into the osteochondral defects of rabbits. QDs were conjugated with a unique internalizing antibody against a heat shock protein-70 (hsp70) family stress chaperone, mortalin, which is upregulated and expressed on the surface of dividing cells. The i-QDs were added to the culture medium for 24 h. Scaffold-free cartilaginous aggregates formed from i-QD-labelled MSCs (i-MSCs), using a 3D culture system with chondrogenic supplements for 1 week, were transplanted into osteochondral defects of rabbits. At 4, 8 and 26 weeks after the transplantation, the reparative tissues were evaluated macroscopically, histologically and fluoroscopically. At as early as 4 weeks, the defects were covered with a white tissue resembling articular cartilage. In histological appearance, the reparative tissues resembled hyaline cartilage on safranin-O staining throughout the 26 weeks. In the deeper portion, subchondral bone and bone marrow were well remodelled. On fluoroscopic evaluation, QDs were tracked mainly in bone marrow stromata, with some signals detected in cartilage and the subchondral bone layer. We showed that the labelling of rabbit MSCs with anti-mortalin antibody-conjugated i-QDs is a tolerable procedure and provides a stable fluorescence signal during the cartilage repair process for up to 26 weeks after transplantation. The results suggest that i-MSCs did not inhibit, and indeed contributed to, the regeneration of osteochondral defects.
机译:这项研究的目的是在将三维(3D)软骨聚集物同种异体移植到兔的骨软骨缺损后,追踪修复组织中带有内在化量子点(i-QDs)标记的间充质干细胞(MSC)。 QD与抗热休克蛋白70(hsp70)家族应激伴侣,凡他林的独特内在化抗体缀合,后者被上调并在分裂细胞表面表达。将i-QDs添加到培养基中24小时。由i-QD标记的MSC(i-MSC)形成的无支架软骨聚集体,使用带有软骨生成补充剂的3D培养系统培养1周,移植到兔的骨软骨缺损中。移植后第4、8和26周,用肉眼,组织学和荧光检查法评估修复组织。早在4周时,缺损就被类似关节软骨的白色组织覆盖。在组织学外观上,在整个26周内,经番红素O染色后,修复组织类似于透明软骨。在更深的部分,软骨下骨和骨髓被很好地重塑。通过荧光检查评估,QD主要在骨髓基质中被追踪,在软骨和软骨下骨层中检测到一些信号。我们表明,抗-凡尔林抗体偶联的i-QDs标记兔MSC是可耐受的程序,在移植后长达26周的软骨修复过程中提供了稳定的荧光信号。结果表明,i-MSCs并没有抑制骨软骨缺损的再生,并确实有助于骨软骨缺损的再生。

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