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首页> 外文期刊>Cell and Tissue Research >Effects of TGF-beta1 on the proliferation and differentiation of human periodontal ligament cells and a human periodontal ligament stem/progenitor cell line.
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Effects of TGF-beta1 on the proliferation and differentiation of human periodontal ligament cells and a human periodontal ligament stem/progenitor cell line.

机译:TGF-beta1对人牙周膜细胞和人牙周膜干/祖细胞系增殖和分化的影响。

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Periodontal ligament (PDL) is a specialized connective tissue that influences the lifespan of the tooth. Transforming growth factor-beta1 (TGF-beta1) is a multifunctional cytokine, but little is known about the effects of TGF-beta1 on PDL cells. Our aim has been to demonstrate the expression of TGF-beta1 in rat PDL tissues and to evaluate its effects on the proliferation and gene expression in human PDL cells (HPLCs) and a human PDL stem/progenitor cell line, line 1-11, that we have recently developed. The expression of TGF-beta1 in the entire PDL tissue was confirmed immunohistochemically, and both HPLCs and cell line 1-11 expressed mRNA from the TGF-beta1, TGF-beta type I receptor, and TGF-beta type II receptor genes. Although exogenous TGF-beta1 stimulated the proliferation of HPLCs, it did not upregulate the expression of alpha-smooth muscle actin (alpha-SMA), type I collagen (Col I), or fibrillin-1 (FBN1) mRNA or of alpha-SMA protein in HPLCs, whereas expression for these genes was attenuated by an anti-TGF-beta1 neutralizing antibody. In contrast, exogenous TGF-beta1 reduced the proliferation of cell line 1-11, although it upregulated the expression of alpha-SMA, Col I, and FBN1 mRNA and of alpha-SMA protein in this cell line. In addition, interleukin-1 beta stimulation significantly reduced the expression of TGF-beta1 mRNA and protein in HPLCs. Thus, TGF-beta1 seems to play an important role in inducing fibroblastic differentiation of PDL stem/progenitor cells and in maintaining the PDL apparatus under physiological conditions.
机译:牙周膜(PDL)是一种特殊的结缔组织,会影响牙齿的寿命。转化生长因子-beta1(TGF-beta1)是一种多功能的细胞因子,但对于TGF-beta1对PDL细胞的作用知之甚少。我们的目的是证明TGF-beta1在大鼠PDL组织中的表达,并评估其对人PDL细胞(HPLC)和人PDL干/祖细胞系1-11行中增殖和基因表达的影响,我们最近开发了。免疫组织化学证实了TGF-beta1在整个PDL组织中的表达,HPLC和细胞系1-11均表达了来自TGF-beta1,TGF-beta I型受体和TGF-beta II型受体基因的mRNA。尽管外源性TGF-beta1刺激了HPLC的增殖,但它并未上调α平滑肌肌动蛋白(alpha-SMA),I型胶原蛋白(Col I)或fibrillin-1(FBN1)mRNA或alpha-SMA的表达高效液相色谱中的蛋白,而抗TGF-β1中和抗体减弱了这些基因的表达。相反,外源性TGF-beta1减少了细胞系1-11的增殖,尽管它上调了该细胞系中α-SMA,Col I和FBN1 mRNA的表达以及α-SMA蛋白。此外,白介素-1β刺激显着降低了HPLC中TGF-β1mRNA和蛋白质的表达。因此,TGF-β1似乎在诱导PDL干/祖细胞的成纤维细胞分化以及在生理条件下维持PDL装置中起重要作用。

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