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Characterisation of the constitutive over-expression of AJ18 in a novel rat stromal bone marrow cell line (D8-SBMC)
Authors:Andrew Jheon  Baoqian Zhu  Sela Cheifetz
Affiliation:a Department of Orthopaedic Surgery, University of California at San Francisco, 533 Parnassus Ave. U470, San Francisco, CA 94143, United States
b Nova Century Scientific Inc., 5022 South Service Road, Burlington, ON, Canada L7L 5Y7
c CIHR Group in Matrix Dynamics, University of Toronto, 150 College St. #234, Toronto, ON, Canada M5S 3E2
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.
Keywords:AS, antisense   AA, ascorbic acid   β-GP, beta-glycerophosphate   BMP, bone morphogenetic protein   BSP, bone sialoprotein   CMV, cytomegalovirus   COL1, collagen type 1   D8-SBMC, D8-stromal bone marrow cell   Dex, dexamethasone   EV, empty vector   FRCC, foetal rat cavarial cell   FGF-2, fibroblast growth factor-2   HA, hydroxyapatite   KRAB, Krü  ppel-associated box   MEM, minimal essential medium   OSE2, osteoblast-specific element 1   OC, osteocalcin   OPN, osteopontin   Osx, osterix   RBMC, rat bone marrow cell   SPARC, secreted protein acidic and rich in cysteine   S, sense   TNAP, tissue non-specific alkaline phosphatase   TEM, transmission electron microscopy   WT, wild type
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