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流体流动以时间依赖性方式刺激骨髓基质细胞表达骨桥蛋白和骨唾液酸蛋白。

Fluid flow stimulates expression of osteopontin and bone sialoprotein by bone marrow stromal cells in a temporally dependent manner.

作者信息

Kreke Michelle R, Huckle William R, Goldstein Aaron S

机构信息

Department of Chemical Engineering, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061-0211, USA.

出版信息

Bone. 2005 Jun;36(6):1047-55. doi: 10.1016/j.bone.2005.03.008.

Abstract

Bone marrow stromal cells (BMSCs) are multipotent progenitor cells with a capacity to form bone tissue in vivo, and to differentiate into the osteoblastic lineage in vitro. Drawing on evidence that bone is mechanosensitive and mechanical stimuli are anabolic, we postulate that proliferation and osteoblastic differentiation of BMSCs may be stimulated by mechanical forces. In this study, BMSCs cultured in the presence of osteogenic factors (dexamethasone, beta-glycerophosphate, and ascorbate) were stimulated repeatedly (every second day) with shearing flow (1.6 dyn/cm(2)) for 5, 30, or 120 min, and assayed for systematic changes in cell number and phenotypic markers of osteoblastic differentiation. Cells exposed to fluid flow on days 2 and 4 after the addition of osteogenic factors and assayed at day 6 exhibited a modest decrease in cell number and increase in normalized alkaline phosphatase activity, suggesting the detachment of a non-osteogenic subpopulation. Cells exposed to fluid flow on days 6, 8, 10, and 12 and assayed at day 20 demonstrated maximal expression of osteopontin and bone sialoprotein mRNA with 30 min duration of flow. Concurrently, at day 20 expression of the adipogenic marker, lipoprotein lipase, was minimal with a 120-min duration of flow. These results indicate that repeated application of shear stress stimulates late phenotypic markers of osteoblastic differentiation of BMSCs in a manner that depends on the duration of stimulus. Finally, accumulation of prostaglandin E(2) in culture medium in response to shearing flow systematically decreased with repeated exposure to 30 and 120 min of shear stress (from day 6 to day 12), suggesting an adaptation of the cells to fluid flow.

摘要

骨髓基质细胞(BMSCs)是多能祖细胞,具有在体内形成骨组织以及在体外分化为成骨细胞谱系的能力。基于骨骼具有机械敏感性且机械刺激具有合成代谢作用的证据,我们推测机械力可能刺激BMSCs的增殖和成骨细胞分化。在本研究中,在成骨因子(地塞米松、β-甘油磷酸酯和抗坏血酸盐)存在下培养的BMSCs每隔一天被剪切流(1.6达因/平方厘米)反复刺激5、30或120分钟,并检测细胞数量和成骨细胞分化表型标志物的系统性变化。在添加成骨因子后第2天和第4天暴露于流体流动并在第6天进行检测的细胞,其细胞数量适度减少,标准化碱性磷酸酶活性增加,这表明一个非成骨亚群的脱离。在第6、8、10和12天暴露于流体流动并在第20天进行检测的细胞,在30分钟的流动持续时间下显示骨桥蛋白和骨唾液蛋白mRNA的最大表达。同时,在第20天,脂肪生成标志物脂蛋白脂肪酶在120分钟的流动持续时间下表达最低。这些结果表明,反复施加剪切应力以一种依赖于刺激持续时间的方式刺激BMSCs成骨细胞分化的晚期表型标志物。最后,随着反复暴露于30分钟和120分钟的剪切应力(从第6天到第12天),培养基中前列腺素E2因剪切流的积累系统性地减少,这表明细胞对流体流动产生了适应性。

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