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ISSN : 1226-7155(Print)
ISSN : 2287-6618(Online)
International Journal of Oral Biology Vol.33 No.3 pp.105-111
DOI :

Thrombospondins Mediate the Adhesion of Osteoblast to Extracelluar Matrix

Jeong-Tae Koh, Lim Dong-Jin, Bae In-Ho, Jeong Byung-Chul, Kim Sun-Hun, Park Bae-Keun, Kang In-Chul, Lee Shee-Eun, Song Sang-Hun
Dept. of Pharmacology and Dental Therapeutics, Chonnam National University
Biomedical Research Center, Ulsan University Hospital
Dental Science Research Institute and BK21 Project for Dentistry, Chonnam National University
Department of Oral & Maxillofacial Surgery, College of Medicine, Hallym Univ. Medical center

Abstract

Thrombospondins (TSP-1, TSP-2) are secretory extracellular glycoproteins that are involved in a variety of physiological processes such as tumor cell adhesion, invasion, and metastasis. The present study was undertaken to elucidate the involvement of thrombospondins in the adhesion of osteoblast-like cells using the TSP-1 or TSP-2 antisense MG63 and MC3T3-E1 cell lines. For downregulation of TSPs expression, we prepared antisense constructs for TSP-1 and TSP-2 using the pREP4 an episomal mammalian expression vector, which be able to produce the specific antisense oligonucleotides around chromosome. MG63 and MC3T3-E1 osteoblast-like cells were transfected with the antisense constructs and nonliposomal Fugene 6, and then selected under hygromycin B (50 μM/mℓ) treatment for 2 weeks. Western blot analysis revealed that expression of the TSP proteins was downregulated in the antisense cell lines. The cell adhesion assay showed that adhesive properties of TSP-1 and TSP-2 antisense MG63 cells on the polystyrene culture plate were reduced to 17% and 21% of the control cells, respectively, and those of the TSP-1 and TSP-2 antisense MC3T3-E1 cells also decreased to 19% and 27% of control, respectively. Adhesion of TSP-1 and TSP-2 antisense MC3T3-E1 cells on Type I collagen-coated culture plate decreased to 27% and 76%, respectively. These results indicate that TSP-1 and TSP-2 proteins may have an important role in adhesion of osteoblast-like cells to extracellular matrix.

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