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一种新型人类转化生长因子-β1融合蛋白与重组人骨形态发生蛋白-2联合使用可增强骨髓间充质干细胞的软骨成骨分化。

A novel human TGF-β1 fusion protein in combination with rhBMP-2 increases chondro-osteogenic differentiation of bone marrow mesenchymal stem cells.

作者信息

Claros Silvia, Rico-Llanos Gustavo A, Becerra José, Andrades José A

机构信息

Laboratory of Bioengineering and Tissue Regeneration (LABRET), Department of Cell Biology, Genetics and Physiology, Faculty of Sciences, Universidad de Málaga, Campus de Teatinos, Málaga 29071, Spain.

出版信息

Int J Mol Sci. 2014 Jun 25;15(7):11255-74. doi: 10.3390/ijms150711255.

DOI:10.3390/ijms150711255
PMID:24968268
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4139781/
Abstract

Transforming growth factor-beta (TGF-β) is involved in processes related to the differentiation and maturation of osteoprogenitor cells into osteoblasts. Rat bone marrow (BM) cells were cultured in a collagen-gel containing 0.5% fetal bovine serum (FBS) for 10 days in the presence of rhTGF (recombinant human TGF)-β1-F2, a fusion protein engineered to include a high-affinity collagen-binding decapeptide derived from von Willebrand factor. Subsequently, cells were moderately expanded in medium with 10% FBS for 4 days and treated with a short pulse of rhBMP (recombinant human bone morphogenetic protein)-2 for 4 h. During the last 2 days, dexamethasone and β-glycerophosphate were added to potentiate osteoinduction. Concomitant with an up-regulation of cell proliferation, DNA synthesis levels were determined. Polymerase chain reaction was performed to reveal the possible stemness of these cells. Osteogenic differentiation was evaluated in terms of alkaline phosphatase activity and mineralized matrix formation as well as by mRNA expression of osteogenic marker genes. Moreover, cells were placed inside diffusion chambers and implanted subcutaneously into the backs of adult rats for 4 weeks. Histological study provided evidence of cartilage and bone-like tissue formation. This experimental procedure is capable of selecting cell populations from BM that, in the presence of rhTGF-β1-F2 and rhBMP-2, achieve skeletogenic potential in vitro and in vivo.

摘要

转化生长因子-β(TGF-β)参与与骨祖细胞分化和成熟为成骨细胞相关的过程。将大鼠骨髓(BM)细胞在含有0.5%胎牛血清(FBS)的胶原凝胶中培养10天,培养过程中加入rhTGF(重组人TGF)-β1-F2,这是一种经过工程改造的融合蛋白,包含源自血管性血友病因子的高亲和力胶原结合十肽。随后,细胞在含有10% FBS的培养基中适度扩增4天,并用rhBMP(重组人骨形态发生蛋白)-2短脉冲处理4小时。在最后2天,加入地塞米松和β-甘油磷酸以增强骨诱导作用。伴随着细胞增殖的上调,测定DNA合成水平。进行聚合酶链反应以揭示这些细胞可能的干性。根据碱性磷酸酶活性、矿化基质形成以及成骨标记基因的mRNA表达来评估成骨分化。此外,将细胞置于扩散小室中,皮下植入成年大鼠背部4周。组织学研究提供了软骨和类骨组织形成的证据。该实验程序能够从骨髓中选择细胞群体,这些细胞群体在rhTGF-β1-F2和rhBMP-2存在的情况下,在体外和体内均具有成骨潜能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c090/4139781/68c9a899e4d8/ijms-15-11255-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c090/4139781/39d261cca86b/ijms-15-11255-g001.jpg
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