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Studies on Connexin 43, a Gap-Junction Protein, in P19 Embryonal Carcinoma Cells after Culture on an Apatite Fiber Scaffold

机译:在磷灰石纤维支架上培养后P19胚胎癌细胞中的Connexin 43,间隙结蛋白

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We previously showed enhanced osteoblast differentiation by culturing cells in apatite-fiber scaffold (AFS). The well-developed α-surface of the apatite fibers provides favorable structural features and chemical interactions with the cells, and the scaffold appears to affect cell differentiation. AFS was used here to study its utility for soft-tissue engineering. An embryonal carcinoma cell line, P19.CL6, was cultured in AFS, and the expression and phosphorylation of a gap-junction protein, connexin 43 (Cx43), during cell proliferation and differentiation was examined. We show that treatment with dimethyl sulfoxide appears to induce a change in the isoform composition of Cx43 under the control condition, but not in AFS. We also show that serum starvation induces the phosphorylation of Ser 368 of Cx43 only in functionally mature cells.
机译:我们以前通过在磷灰石 - 纤维支架(AFS)中培养细胞来表现出增强的成骨细胞分化。磷灰石纤维的良好α-表面提供有利的结构特征和与细胞的化学相互作用,并且支架似乎影响细胞分化。这里使用AFS研究其对软组织工程的效用。检查胚胎癌细胞系P19.Cl6,在AFS中培养,以及间隙结蛋白,Connexin 43(CX43),在细胞增殖和分化期间的表达和磷酸化。我们表明,用二甲基亚砜处理似乎在对照条件下诱导CX43的同种型组合物的变化,但不在AFS中。我们还表明,血清饥饿仅在功能性成熟的细胞中诱导CX43的SER 368的磷酸化。

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