首页> 外文期刊>Journal of Molecular and Cellular Cardiology >Regulated expression of a contractile protein gene correlates with recovery of contractile function after reversible metabolic inhibition in cultured myocytes.
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Regulated expression of a contractile protein gene correlates with recovery of contractile function after reversible metabolic inhibition in cultured myocytes.

机译:收缩蛋白基因的调节表达与培养的肌细胞中可逆代谢抑制后收缩功能的回收率相关。

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Little is known of the relation between recovery of contraction and the regulation of contractile protein gene expression in ventricular myocytes after severe ATP depletion. We have examined alterations in activation of an MLC-2 luciferase fusion gene in cultured neonatal rat ventricular myocytes produced by exposure to 2 mM Na CN and 20 mM 2-deoxyglucose, and after recovery is serum or serum free medium. The effects of metabolic inhibition followed by recovery on expression on an RSV-luciferase activity were also investigated. Myocytes were co-transfected with a CMV beta-galactosidase fusion gene, and luciferase activities were normalized relative to beta-galactosidase activity to control for transfection efficiency. Two hours of metabolic inhibition produced significant cell injury, as documented by disorganization of myofilaments, and reduction in luciferase and beta-galactosidase activity within transfected cells. Cells allowed to recover for 48 h in serum free hormone supplemented medium showed a further decline in corrected luciferase activity, consistent with a marked reduction in MLC-2 gene transcription. Cells recovered from severe metabolic inhibition in serum free medium also showed failure to redevelop contractile activity, and failure of redevelopment of organized myofibrils. In contrast, myocytes exposed to serum during the 48 h recovery period had a marked increase in luciferase activity, resumed contractile activity and re-established organized myofilaments. There were no significant differences between RSV luciferase activities in cells recovered in serum versus serum free media. In ventricular myocytes in which contraction was inhibited by exposure to 10 microM verapamil, MLC-2 luciferase activity declined by 87%. However, even when contractile activity was inhibited by exposure to verapamil during recovery from metabolic inhibition, exposure to serum containing medium caused a significantly greater increase in MLC-2 luciferase activity than did serum free medium. Thus, the effects of serum on MLC-2 gene expression were not solely due to an effect of serum on recovery of contractile activity. Verapamil had no consistent effect on expression of RSV luciferase. These results suggest that expression of the MLC-2 gene is markedly reduced following recovery from severe metabolic inhibition, an effect largely due to cessation of myocyte contractile activity. Resupply of growth factors present in fetal calf serum reactivate expression of this gene, and this is associated with resumption of contractile activity and redevelopment of organized myofibrils. These results suggest that reactivation of contractile protein gene expression during recovery from metabolic inhibition may be beneficial in allowing cells to recover from this insult.
机译:在严重ATP耗尽后,恢复收缩恢复与收缩蛋白质基因表达的关系毫无少的关系。我们研究了通过暴露于2mM Na CN和20mM 2-脱氧葡萄糖产生的培养的新生大鼠心室肌细胞中MLC-2荧光素酶融合基因的改变,并且在回收是血清或无血清培养基之后。还研究了代谢抑制作用的影响,然后进行了对RSV-荧光素酶活性的表达恢复。用CMVβ-半乳糖苷酶融合基因共转染肌细胞,并且荧光素酶活性相对于β-半乳糖苷酶活性归一化以控制转染效率。两小时的代谢抑制产生了显着的细胞损伤,如氰瘤菌的紊乱所记录的,以及转染细胞内的荧光素酶和β-半乳糖苷酶活性的减少。在血清自由激素中恢复48小时的细胞在补充培养基中,校正的荧光素酶活性进一步下降,与MLC-2基因转录的标记降低一致。在血清自由培养基中从严重代谢抑制中回收的细胞也表现出未结合的收缩活性,并且有组织的肌原纤维的重建失败。相比之下,在48h恢复期间暴露于血清的肌细胞具有显着的荧光素酶活性的增加,恢复收缩活性并重新建立有组织的肌细胞。在血清中回收的细胞与血清自由培养基中回收的细胞中没有显着差异。在室外肌细胞中,通过暴露于10微米的维拉帕米抑制收缩,MLC-2荧光素酶活性下降87%。然而,即使在从代谢抑制期间通过暴露于维拉帕米抑制收缩活性时,含有血清培养基的暴露导致MLC-2荧光素酶活性的显着增加显着增加,而不是血清自由培养基。因此,血清对MLC-2基因表达的影响不仅是由于血清对收缩活性恢复的影响。维拉帕米对RSV荧光素酶表达没有一致的影响。这些结果表明MLC-2基因的表达显着降低,在严重的代谢抑制后,在恢复后显着降低,其效果主要是由于肌细胞收缩活性的停止。胎牛血清中存在的生长因子再补充是该基因的表达,这与收缩活性的恢复和组织肌原纤维的重建有关。这些结果表明,从代谢抑制中恢复期间收缩蛋白基因表达的再活化可能是有益的,允许细胞从这种侮辱中恢复。

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