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在体内异位构建具有解剖形状的人关节髁组织形成和血管化。

Tissue formation and vascularization in anatomically shaped human joint condyle ectopically in vivo.

机构信息

Tissue Engineering and Regenerative Medicine Laboratory, Columbia University Medical Center, New York, New York 10032, USA.

出版信息

Tissue Eng Part A. 2009 Dec;15(12):3923-30. doi: 10.1089/ten.TEA.2008.0653.

Abstract

Scale-up of bioengineered grafts toward clinical applications is a challenge in regenerative medicine. Here, we report tissue formation and vascularization of anatomically shaped human tibial condyles ectopically with a dimension of 20 x 15 x 15 mm(3). A composite of poly-epsilon-caprolactone and hydroxyapatite was fabricated using layer deposition of three-dimensional interlaid strands with interconnecting microchannels (400 microm) and seeded with human bone marrow stem cells (hMSCs) with or without osteogenic differentiation. An overlaying layer (1 mm deep) of poly(ethylene glycol)-based hydrogel encapsulating hMSCs or hMSC-derived chondrocytes was molded into anatomic shape and anchored into microchannels by gel infusion. After 6 weeks of subcutaneous implantation in athymic rats, hMSCs generated not only significantly more blood vessels, but also significantly larger-diameter vessels than hMSC-derived osteoblasts, although hMSC-derived osteoblasts yielded mineralized tissue in microchannels. Chondrocytes in safranin-O-positive glycosaminoglycan matrix were present in the cartilage layer seeded with hMSC-derived chondrogenic cells, although significantly more cells were present in the cartilage layer seeded with hMSCs than hMSC-derived chondrocytes. Together, MSCs elaborate substantially more angiogenesis, whereas their progenies yield corresponding differentiated tissue phenotypes. Scale up is probable by incorporating a combination of stem cells and their progenies in repeating modules of internal microchannels.

摘要

生物工程移植物向临床应用的规模化是再生医学面临的挑战。在这里,我们报告了使用三维交错丝层沉积法制造的聚己内酯和羟基磷灰石复合材料,该方法具有互连的微通道(400 微米),并接种了或未经成骨分化的人骨髓基质细胞(hMSCs)。覆盖层(1 毫米深)由基于聚乙二醇的水凝胶构成,其中包埋了 hMSCs 或 hMSC 来源的软骨细胞,并通过凝胶注入成型为解剖形状并锚定到微通道中。在无胸腺大鼠的皮下植入 6 周后,hMSCs 不仅产生了更多的血管,而且与 hMSC 来源的成骨细胞相比,血管直径也更大,尽管 hMSC 来源的成骨细胞在微通道中产生了矿化组织。在接种了 hMSC 来源的软骨形成细胞的软骨层中存在着软骨素-O 阳性糖胺聚糖基质中的软骨细胞,尽管在接种了 hMSCs 的软骨层中存在的细胞显著多于 hMSC 来源的软骨细胞。总之,MSCs 产生了大量的血管生成,而它们的后代则产生了相应的分化组织表型。通过将干细胞及其后代组合在内部微通道的重复模块中,可能会实现规模化。

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