首页> 美国卫生研究院文献>Biochemical Journal >Transfection of L6 myoblasts with adipocyte fatty acid-binding protein cDNA does not affect fatty acid uptake but disturbs lipid metabolism and fusion.
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Transfection of L6 myoblasts with adipocyte fatty acid-binding protein cDNA does not affect fatty acid uptake but disturbs lipid metabolism and fusion.

机译:用脂肪细胞脂肪酸结合蛋白cDNA转染L6成肌细胞不会影响脂肪酸摄取但会干扰脂质代谢和融合。

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摘要

We studied the involvement of fatty acid-binding protein (FABP) in growth, differentiation and fatty acid metabolism of muscle cells by lipofection of rat L6 myoblasts with rat heart (H) FABP cDNA or with rat adipocyte (A) FABP cDNA in a eukaryotic expression vector which contained a puromycin acetyltransferase cassette. Stable transfectants showed integration into the genome for all constructs and type-specific overexpression at the mRNA and protein level for the clones with H-FABP and A-FABP cDNA constructs. The rate of proliferation of myoblasts transfected with rat A-FABP cDNA was 2-fold higher compared with all other transfected cells. In addition, these myoblasts showed disturbed fusion and differentiation, as assessed by morphological examination and creatine kinase activity. Uptake rates of palmitate were equal for all clone types, in spite of different FABP content and composition. Palmitate oxidation over a 3 h period was similar in all clones from growth medium. After being cultured in differentiation medium, mock- and H-FABP-cDNA-transfected cells showed a lower fatty acid-oxidation rate, in contrast with A-FABP-cDNA-transfected clones. The ratio of [14C]palmitic acid incorporation into phosphatidylcholine and phosphatidylethanolamine of A-FABP-cDNA-transfected clones changed in the opposite direction in differentiation medium from that of mock- and H-FABP-cDNA-transfected clones. In conclusion, transfection of L6 myoblasts with A-FABP cDNA does not affect H-FABP content and fatty acid uptake, but changes fatty acid metabolism. The latter changes may be related to the observed fusion defect.
机译:我们研究了脂肪酸结合蛋白(FABP)在真核生物中通过大鼠心脏(H)FABP cDNA或大鼠脂肪细胞(A)FABP cDNA脂质转染大鼠L6成肌细胞而参与肌肉细胞生长,分化和脂肪酸代谢的过程。表达载体,其中含有嘌呤霉素乙酰转移酶盒。稳定的转染子显示出所有构建体均已整合到基因组中,而具有H-FABP和A-FABP cDNA构建体的克隆在mRNA和蛋白质水平上均表现出类型特异性过表达。与所有其他转染细胞相比,用大鼠A-FABP cDNA转染的成肌细胞的增殖速率高2倍。此外,如通过形态学检查和肌酸激酶活性评估,这些成肌细胞显示出混乱的融合和分化。尽管FABP含量和组成不同,但所有克隆类型的棕榈酸酯摄取率均相等。 3 h期间棕榈酸酯在来自生长培养基的所有克隆中的氧化相似。与A-FABP-cDNA转染的克隆相比,在分化培养基中培养后,模拟和H-FABP-cDNA转染的细胞显示出较低的脂肪酸氧化率。 A-FABP-cDNA转染的克隆中[14C]棕榈酸掺入磷脂酰胆碱和磷脂酰乙醇胺的比例在分化培养基中与模拟和H-FABP-cDNA转染的克隆相反。总之,用A-FABP cDNA转染L6成肌细胞不会影响H-FABP含量和脂肪酸摄取,但会改变脂肪酸代谢。后者的变化可能与观察到的融合缺陷有关。

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