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Synergistic interaction of hTGF-β 3 with hBMP-6 promotes articular cartilage formation in chitosan scaffolds with hADSCs: implications for regenerative medicine

机译:HTGF-β3与HBMP-6的协同相互作用促进了壳聚糖支架的关节软骨形成:对再生医学的影响

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Human TGF-β3 has been used in many studies to induce genes coding for typical cartilage matrix components and accelerate chondrogenic differentiation, making it the standard constituent in most cultivation media used for the assessment of chondrogenesis associated with various stem cell types on carrier matrices. However, in vivo data suggests that TGF-β3 and its other isoforms also induce endochondral and intramembranous osteogenesis in non-primate species to other mammals. Based on previously demonstrated improved articular cartilage induction by a using hTGF-β3 and hBMP-6 together on hADSC cultures and the interaction of TGF- β with matrix in vivo, the present study investigates the interaction of a chitosan scaffold as polyanionic polysaccharide with both growth factors. The study analyzes the difference between chondrogenic differentiation that leads to stable hyaline cartilage and the endochondral ossification route that ends in hypertrophy by extending the usual panel of investigated gene expression and stringent employment of quantitative PCR. By assessing the viability, proliferation, matrix formation and gene expression patterns it is shown that hTGF-β3? ?hBMP-6 promotes improved hyaline articular cartilage formation in a chitosan scaffold in which ACAN with Col2A1 and not Col1A1 nor Col10A1 where highly expressed both at a transcriptional and translational level. Inversely, hTGF-β3 alone tended towards endochondral bone formation showing according protein and gene expression patterns. These findings demonstrate that clinical therapies should consider using hTGF-β3? ?hBMP-6 in articular cartilage regeneration therapies as the synergistic interaction of these morphogens seems to ensure and maintain proper hyaline articular cartilage matrix formation counteracting degeneration to fibrous tissue or ossification. These effects are produced by interaction of the growth factors with the polysaccharide matrix.
机译:人TGF-β3已被用于许多研究中,以诱导编码典型软骨基质组分的基因,并加速软骨内分化,使其成为大多数培养介质中的标准成分,用于评估与载体基质上的各种干细胞类型相关的软骨发生。然而,体内数据表明TGF-β3及其其他同种型也诱导非灵长类动物的中间细胞和肠腔骨质骨发生给其他哺乳动物。基于先前证明了使用HTGF-β3和HBMP-6在哈姆斯培养物中的改进的关节软骨诱导和TGF-β与体内基质的相互作用,本研究研究了壳聚糖支架作为聚阴离子多糖的相互作用,两种生长因素。该研究分析了软骨细胞分化之间的差异,导致稳定的透明软骨和中端骨化途径,通过延长常规的研究基因表达和定量PCR的严格就业而在肥大中终止肥大。通过评估活力,增殖,基质形成和基因表达模式,显示HTGF-β3? ?HBMP-6在壳聚糖支架中促进改善的透明关节软骨形成,其中COL2A1和COL1A1也不是COL10A1,其中在转录和平移水平上高度表达。同样地,单独的HTGF-β3倾向于蛋白质和基因表达模式的中间骨形成。这些研究结果表明,临床治疗应该考虑使用HTGF-β3?在关节软骨再生疗法中的HBMP-6似乎这些转基因的协同相互作用似乎确保并保持了适当的透明关节软骨基质形成抵消了纤维组织或骨化的变性。这些效果是通过与多糖基质的生长因子的相互作用产生的。

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