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The Effect of TGF-¥â1 on Cellular Activity of Periodontal Ligament Cells activated by PDGF-BB

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Abstract


The purposes of this study is to evaluate the combination effects of TGF-¥â1 and PDGF-BB on the periodontal ligament cells to use as a regeneration promoting agent of periodontal tissue. Human periodontal ligament cells were prepared from the first premolar tooth extracted for the orthodontic treatment and were cultured in DMEM/10% FBS at the 37¡É, 5% CO2 incubator. Authors measured the DNA synthesis, total protein, collagen and noncollagenous protein synthesis according to the concentration of TGF-¥â1, (1, 5ng/ml) and PDGF-BB (1, 10 ng/ml) in combination. To explore further this delayed effect of TGF-¥â1, we preincubated human periodontal ligament cells with TGF-¥â1 for 4 or 24 hours before PDGF-BB stimulation.

The results were as follows:

The DNA synthetic activity was increased dose dependently by TGF-¥â1, PDGF-BB. The combination of TGF-¥â1 and PDGF-BB consistently enhanced the DNA synthetic activity to PDGF-BB alone. The ability of TGF-¥â1 to enhance DNA synthetic activity in PDGF-BB treated periodontal ligament cells was dose dependent. The maximum mitogenic effect was at the 5ng/ml of TGF-¥â1 and 10ng/ml of PDGF-BB. Preincubation of cells with TGF-¥â1 resulted in significantly greater response to PDGF-BB at all TGF-¥â1 concentration studied, and may be useful for clinical application in periodontal regenerative procedures. The total protein, collagen and noncollagen synthesis was increased dose pendently by TGF-¥â1, PDGF-BB. The % of collagen was slightly decresed according to the concentration of TGF-¥â1, PDGF-BB. The effect of TGF-¥â1, PDGF-BB were not specific for collagen synthesis since it also increased noncollagenous protein synthesis.

This study demonstrates that PDGF-BB is major mitogens for human periodontal ligament cells in vitro, and supports a role for TGF-¥â1 as a regulation of the mitogenic and total protein formation to PDGF-BB in these cells.

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