Vimentin Expression in Osteoblasts in Response to Cyclic Mechanical Strain The cyroskeleton is a filamentous protein network that extends throughout the cytoplasm of eukaryotic cells. Intermediate filaments are tissue-specific cytoskeletal proteins that are thought to play a structural or tension bearing role in the cell. To test this possibility, we examined vimentin, an intermediate filament protein that is expressed in a variety of cells including osteoblasts, by immunoprecipitation and immunofluorescent confocial microscopy. Calvarial explants were dissected from 12-day old chick embryos and grown for 14 days in vitro. Osteoblasts were plated at a density of 5 x 104 cells/ml onto control or flexible bottomed cell culture plates. The FlexercellTM. Strain Unit was utilized to deliver the strain regimen which consisted of 3 control cells were either fixed and immunostained for scanning confocal laser microscopy, or pulse- labeled with [35S] methionine and immunoprecipitated with an antivimentin monoclonal antibody. TCA precipitation was also performed to analyze total protein synthesis. Immunostaining reveals an increase in the vimentin protein throughout the cells following 24, 48, and 72 hours of strain. Furthermore, the vimentin compared with controls. Quantitatively, total protein synthesis increased after 24, 48, and 72 hours of strain. Vimentin protein synthesis also increased after 24 and 48 hours of strain, while after 72 hours of strain, a decrease in vimentin was noted. These studies indicate that changes in vimentin synthesis and organization may play a role in osteoblast response to strain. This model system will allow us to explore the potential of a direct structure-function relationship of various cytoskeletal proteins in bone response to stress. Key Words: Vimentin, Osteoblast

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Unknown (K16)
Project #
5K16DE000175-10
Application #
3753469
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
10
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Iowa
Department
Type
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Perinpanayagam, H; Schneider, G; Holtman, K et al. (2004) Altered Cbfa1 expression and biomineralization in an osteosarcoma cell line. J Orthop Res 22:404-10
Armstrong, Steven R; Vargas, M A; Chung, I et al. (2004) Resin-dentin interfacial ultrastructure and microtensile dentin bond strength after five-year water storage. Oper Dent 29:705-12
Timmons, Sherry R; Nwankwo, Joseph O; Domann, Frederick E (2002) Acetaldehyde activates Jun/AP-1 expression and DNA binding activity in human oral keratinocytes. Oral Oncol 38:281-90
Armstrong, S R; Keller, J C; Boyer, D B (2001) The influence of water storage and C-factor on the dentin-resin composite microtensile bond strength and debond pathway utilizing a filled and unfilled adhesive resin. Dent Mater 17:268-76
Armstrong, S R; Keller, J C; Boyer, D B (2001) Mode of failure in the dentin-adhesive resin-resin composite bonded joint as determined by strength-based (muTBS) and fracture-based (CNSB) mechanical testing. Dent Mater 17:201-10
Armstrong, S R; Boyer, D B; Keller, J C (1998) Microtensile bond strength testing and failure analysis of two dentin adhesives. Dent Mater 14:44-50
Kurago, Z B; Lutz, C T; Smith, K D et al. (1998) NK cell natural cytotoxicity and IFN-gamma production are not always coordinately regulated: engagement of DX9 KIR+ NK cells by HLA-B7 variants and target cells. J Immunol 160:1573-80
Armstrong, S R; Boyer, D B; Keller, J C et al. (1998) Effect of hybrid layer on fracture toughness of adhesively bonded dentin-resin composite joint. Dent Mater 14:91-8
Baumgardner, K R; Walton, R E; Osborne, J W et al. (1996) Induced hypoxia in rat pulp and periapex demonstrated by 3H-misonidazole retention. J Dent Res 75:1753-60
Kurago, Z B; Smith, K D; Lutz, C T (1995) NK cell recognition of MHC class I. NK cells are sensitive to peptide-binding groove and surface alpha-helical mutations that affect T cells. J Immunol 154:2631-41

Showing the most recent 10 out of 12 publications