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AJ18 在新型大鼠基质骨髓细胞系 (D8-SBMC) 中的组成型过表达的特征。

Characterisation of the constitutive over-expression of AJ18 in a novel rat stromal bone marrow cell line (D8-SBMC).

机构信息

Department of Orthopaedic Surgery, University of California at San Francisco, 533 Parnassus Ave. U470, San Francisco, CA 94143, United States.

出版信息

Arch Oral Biol. 2009 Aug;54(8):705-16. doi: 10.1016/j.archoralbio.2009.04.007. Epub 2009 May 26.

Abstract

OBJECTIVE

The elucidation of the molecular pathways involved in osteoblast proliferation and differentiation has been greatly enhanced by the availability of cell culture model systems. However, many of the current bone cell culture systems suffer from disadvantages such as the inability to generate mineralised bone-like nodules, a transformed genetic background, cell heterogeneity, and a relatively long time frame from cell seeding to mineralisation, often in the order of several weeks. Here we describe the establishment and characterisation of a novel bone cell line named D8-SBMC. As a first demonstration of their potential value, D8-SBMC was utilised to further support a role for AJ18 during osteogenesis.

DESIGN

D8-SBMC was established from a single cell suspension of the previously characterised long term rat stromal bone marrow cells [Kotev-Emeth S, Pitaru S, Pri-Chen S, Savion N. Establishment of a rat long-term culture expressing the osteogenic phenotype: dependence on dexamethasone and FGF-2. Connect Tissue Res 2002;43(4):606-12; Pitaru S, Kotev-Emeth S, Noff D, Kaffuler S, Savion N. Effect of basic fibroblast growth factor on the growth and differentiation of adult stromal bone marrow cells: enhanced development of mineralized bone-like tissue in culture. J Bone Miner Res 1993;8(8):919-29]. AJ18 was constitutively and stably over-expressed in D8-SBMC and analysed.

RESULTS

D8-SBMC possesses the ability to form robust mineralised bone-like nodules within 8 days proceeding cell confluency. Interestingly, a cement line-like matrix is also generated between the culture dish and a basal monolayer of cells. Constitutive and stable over-expression of AJ18 resulted in an increase in cell proliferation and mineralisation. Expression of bone marker genes, such as bone sialoprotein, osteopontin, osteocalcin, collage type 1, and osteonectin, was up-regulated by AJ18 over-expression.

CONCLUSION

A novel bone cell line, D8-SBMC, was established and characterised. D8-SBMC may be a valuable model system for biomineralisation studies. D8-SBMC was utilised to further understand the role of AJ18 in cell proliferation and differentiation during osteogenesis.

摘要

目的

由于细胞培养模型系统的可用性,骨细胞增殖和分化所涉及的分子途径的阐明得到了极大的增强。然而,许多现有的骨细胞培养系统存在一些缺点,例如无法生成矿化的骨样结节、遗传背景的改变、细胞异质性以及从细胞接种到矿化的相对较长时间框架,通常需要数周时间。在这里,我们描述了一种新型骨细胞系 D8-SBMC 的建立和特性。作为其潜在价值的首次证明,D8-SBMC 被用于进一步支持 AJ18 在成骨过程中的作用。

设计

D8-SBMC 是从先前表征的大鼠长期基质骨髓细胞的单细胞悬浮液中建立的[Kotev-Emeth S, Pitaru S, Pri-Chen S, Savion N. 建立表达成骨表型的大鼠长期培养物:依赖于地塞米松和 FGF-2. Connect Tissue Res 2002;43(4):606-12; Pitaru S, Kotev-Emeth S, Noff D, Kaffuler S, Savion N. 碱性成纤维细胞生长因子对成年基质骨髓细胞生长和分化的影响:增强培养中矿化骨样组织的发育。J Bone Miner Res 1993;8(8):919-29]。AJ18 在 D8-SBMC 中稳定且持续过表达,并进行了分析。

结果

D8-SBMC 具有在细胞汇合前 8 天内形成坚固矿化骨样结节的能力。有趣的是,在培养皿和基底单层细胞之间也生成了类似骨胶的基质。AJ18 的组成型和稳定过表达导致细胞增殖和矿化增加。AJ18 过表达上调了骨标志物基因的表达,如骨涎蛋白、骨桥蛋白、骨钙素、胶原 1 型和骨粘连蛋白。

结论

建立并表征了一种新型骨细胞系 D8-SBMC。D8-SBMC 可能是生物矿化研究的有价值的模型系统。D8-SBMC 被用于进一步了解 AJ18 在成骨过程中细胞增殖和分化中的作用。

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