首页> 外文期刊>Biomaterials >Large-scale production of murine embryonic stem cell-derived osteoblasts and chondrocytes on microcarriers in serum-free media.
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Large-scale production of murine embryonic stem cell-derived osteoblasts and chondrocytes on microcarriers in serum-free media.

机译:在无血清培养基中的微载体上大规模生产源自鼠胚胎干细胞的成骨细胞和软骨细胞。

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摘要

The generation of tissue-engineered constructs from stem cells for the treatment of musculoskeletal diseases may have immense impact in regenerative medicine, but there are difficulties associated with stem cell culture and differentiation, including the use of serum. Here we present serum-free protocols for the successful production of murine embryonic stem cell (mESC) derived osteoblasts and chondrocytes on CultiSpher S macroporous microcarriers in stirred suspension bioreactors. Various inoculum forms and agitation rates were investigated. Produced osteogenic cells were implanted ectopically into SCID mice and orthotopically into a murine burr-hole fracture model. Osterix, osteocalcin and collagen type I were upregulated in osteogenic cultures, while aggrecan and collagen type II were upregulated in chondrogenic cultures. Histological analysis using alizarin red S, von Kossa and alcian blue staining confirmed the presence of osteoblasts and chondrocytes, respectively in cultured microcarriers and excised tissue. Finally, implantation of derived cells into a mouse fracture model revealed cellular integration without any tumor formation. Overall, microcarriers may provide a supportive scaffold for ESC expansion and differentiation in a serum-free bioprocess for in vivo implantation. These findings lay the groundwork for the development of clinical therapies for musculoskeletal injuries and diseases using hESCs and iPS cells.
机译:从干细胞产生组织工程化构建体以治疗肌肉骨骼疾病可能会对再生医学产生巨大影响,但与干细胞培养和分化(包括使用血清)相关的困难。在这里,我们介绍了在搅拌悬浮生物反应器中,在CultiSpher S大孔微载体上成功生产鼠类胚胎干细胞(mESC)衍生的成骨细胞和软骨细胞的无血清方案。研究了各种接种形式和搅拌速率。将产生的成骨细胞异位植入SCID小鼠,原位植入鼠毛孔破裂模型。 Osterix,骨钙素和I型胶原在成骨培养物中上调,而聚集蛋白聚糖和II型胶原在软骨形成培养物中上调。使用茜素红S,von Kossa和阿尔辛蓝染色的组织学分析证实,培养的微载体和切除的组织中分别存在成骨细胞和软骨细胞。最后,将衍生细胞植入小鼠骨折模型显示细胞整合,没有任何肿瘤形成。总体而言,微载体可以为体内植入的无血清生物过程中的ESC扩展和分化提供支持支架。这些发现为使用hESCs和iPS细胞开发肌肉骨骼损伤和疾病的临床疗法奠定了基础。

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