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首页> 外文期刊>Biomaterials >The effect of licochalcone A on cell-aggregates ECM secretion and osteogenic differentiation during bone formation in metaphyseal defects in ovariectomized rats
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The effect of licochalcone A on cell-aggregates ECM secretion and osteogenic differentiation during bone formation in metaphyseal defects in ovariectomized rats

机译:甘草al烯A对去卵巢大鼠干meta端骨形成过程中骨聚集细胞ECM分泌和成骨分化的影响

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Treatment of weight-bearing bones fractures with defects is critical for patients with osteoporosis's rehabilitation. Although various tissue engineering methods were reported, the best treating strategy for tissue engineering remains to be identified as the limitation of enhancing the ability of the osteogenetic differentiation potential of seed cell is one of the cardinal issues to be solved. The objective of this study is to investigate the feasibility of applying licochalcone-A (L-A) and bone marrow mesenchymal stem cells (BMSC)-aggregate in bone repairing tissue engineering and further study the biological effects of L-A on the cell aggregate formation and osteogenic properties. 80 female SpragueDawley rats underwent bilateral ovariectomy were made with a 3.5mm femurs bone defects without any fixation. These rats were then randomly assigned to five different treatment groups: (1) empty defect (n=16), (2) CA-LA (n=16), (3) CA-N (n=16), (4) CA-L (n=16), (5) CA-S (n=16) and 16 female SD rats were treated as a control. Data showed that L-A administrated cell aggregate had a stronger osteogenic differentiation and mineralized formation potential than non-administrated group both invitro and invivo. For invitro study, L-A administrated group had a more significant expression of ECM, osteogenic associated maker in addition with more mineralized area and higher ALP activity compared with the control group. For invivo study, 3D reconstruction of micro-CT, HE staining and bone strength results showed that newly formed bone in groups administrated by L-A was significant higher than that in Sham group at 2, 4, 8 and 12 weeks after transplantation, especially for groups which was systematically injected with L-A at 8 weeks. Results of our study demonstrated that LA could positively affect cell behavior in cell-aggregate engineering and could be a promising strategy in treating osteoporotic weight-bearing bones fractures with defects.
机译:负重骨骨折的治疗对于骨质疏松症患者的康复至关重要。尽管已经报道了各种组织工程方法,但是仍然需要确定组织工程的最佳治疗策略,因为增强种子细胞成骨分化潜能的能力的局限性是要解决的主要问题之一。这项研究的目的是研究在骨修复组织工程中应用licochalcone-A(LA)和骨髓间充质干细胞(BMSC)聚集体的可行性,并进一步研究LA对细胞聚集体形成和成骨特性的生物学影响。 。 80只雌性SpragueDawley大鼠经双侧卵巢切除术,股骨缺损3.5mm,未进行任何固定。然后将这些大鼠随机分为五个不同的治疗组:(1)空缺损(n = 16),(2)CA-LA(n = 16),(3)CA-N(n = 16),(4)将CA-L(n = 16),(5)CA-S(n = 16)和16只雌性SD大鼠作为对照。数据显示,与非给药组相比,L-A给药的细胞聚集体在体外和体内均具有更强的成骨分化能力和矿化的形成潜力。对于体外研究,与对照组相比,L-A给药组的ECM,成骨相关基因表达水平更高,并且矿化面积更大,ALP活性更高。在体内研究中,micro-CT的3D重建,HE染色和骨强度结果表明,在移植后2、4、8和12周,LA给药组中新形成的骨显着高于Sham组。在第8周系统地注射了LA。我们的研究结果表明,LA可以对细胞聚集工程中的细胞行为产生积极影响,并且可能是治疗有缺陷的骨质疏松负重骨折的有效策略。

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