首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Exogenous proline stimulates type I collagen and HIF-1 alpha expression and the process is attenuated by glutamine in human skin fibroblasts
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Exogenous proline stimulates type I collagen and HIF-1 alpha expression and the process is attenuated by glutamine in human skin fibroblasts

机译:外源性脯氨酸刺激I型胶原蛋白和HIF-1α表达,该方法通过谷氨酰胺在人体皮细胞中衰减

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摘要

Abundance of proline (Pro) in collagen molecule led us to investigate whether Pro supply affects collagen biosynthesis in human skin fibroblasts. Treatment of the cells with milimolar concentrations (5 and 10 mM) of Pro for 24 and 48 h contributed to increase in alpha(1) subunit of collagen type I (COL1A1) expression in both cells and culture medium. However, the effect was more pronounced in glutamine-free medium. In such condition, Pro induced collagen expression by about twofold in the cells, while in the medium only by about 30% during 24 h incubation, compared to control. In the presence of glutamine (Gln), exogenous Pro stimulated intracellular collagen expression only by about 30% during 24 h of fibroblasts incubation, and it was not accompanied by adequate increase of collagen secretion into medium. Gln alone stimulated the processes by about 2-3 fold during the course of the experiment. Pro-dependent increase in collagen expression in Gln-free medium was accompanied by increase in prolidase activity and expression of pAkt. In both Gln-free medium and Gln-supplemented medium, Pro induced expression of p53 and HIF-1 alpha. The data suggest that availability of Gln, as a substrate for Pro biosynthesis, determine the utilization of exogenous Pro for the collagen biosynthesis.
机译:胶原蛋白分子的丰富脯氨酸(Pro)导致我们研究Pro供应是否影响人体皮肤成纤维细胞中的胶原蛋白生物合成。将细胞与微米摩尔浓度(5和10mm)的Pro进行治疗24和48小时,有助于在细胞和培养基中的胶原型I(COL1A1)表达的α(1)亚基的增加。然而,无谷氨酰胺培养基效果更加明显。在这种情况下,通过在细胞中诱导细胞中的胶原蛋白表达,同时在24小时温育期间,在培养基中仅在培养基中孵育约30%。在谷氨酰胺(Gln)的存在下,外源Pro在成纤维细胞孵育中仅刺激细胞内胶原表达约30%,并且不伴随足够的胶原蛋白分泌到培养基中。在实验过程中,Gln独自刺激过程约2-3倍。 GLN-FRES培养基中的胶原蛋白表达的亲依赖性增加伴随着脯氨酸酶活性和PAKT表达的增加。在无华无培养基和GLN补充培养基中,PRO诱导P53和HIF-1α的表达。数据表明,GLN的可用性,作为Pro生物合成的底物,确定外源性Pro用于胶原生物合成的用途。

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