首页> 外文期刊>The Journal of Urology >Contractile protein expression in bladder smooth muscle is a marker of phenotypic modulation after outlet obstruction in the rabbit model.
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Contractile protein expression in bladder smooth muscle is a marker of phenotypic modulation after outlet obstruction in the rabbit model.

机译:膀胱平滑肌中收缩蛋白的表达是兔模型出口阻塞后表型调节的标志。

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PURPOSE: We determined changes in contractile protein expression before and after the relief of partial bladder outlet obstruction in the rabbit model and assessed their potential role as predictors of recovery. MATERIALS AND METHODS: We examined the ratio of the smooth muscle myosin heavy chain isoforms SM2-to-SM1, caldesmon isoform expression and bladder function in obstructed and unobstructed adult rabbit bladders. Cystometry, sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blot analysis were done to determine changes in bladder function and contractile protein expression. RESULTS: Overall we observed significant correlation of bladder weight with the SM2-to-SM1 ratio (p <0.05). Regardless of the duration of obstruction (up to 10 weeks) the ratio appeared to stabilize around a value comparable to that in fetal rabbit smooth muscle cells, suggesting a reversal of SM2 and SM1 expression to a level similar to that at the fetal stage. The pattern of h and l-caldesmon isoform expression showed an increase in l-caldesmon expression in obstructed bladders. Except for decreased leak point pressure in the obstructed group we noted no statistically significant urodynamic changes in bladder capacity or compliance. CONCLUSIONS: There is significant correlation of bladder weight, which is the best known marker of obstruction, with the SM2-to-SM1 ratio. The myosin heavy chain isoform expression ratio appears to be an indicator of phenotypic modulation in bladder smooth muscle before and after the relief of bladder outlet obstruction. Thus, it may be useful as a marker of bladder dysfunction and predictor of functional recovery. Regression to a fetal pattern of protein expression may suggest irreversible damage to smooth muscle cells, possibly limiting recovery.
机译:目的:我们确定了兔子模型中部分膀胱出口梗阻缓解前后收缩蛋白表达的变化,并评估了其作为恢复预测指标的潜在作用。材料与方法:我们检查了成年和未成年成年兔膀胱中平滑肌肌球蛋白重链同工型SM2-SM1的比率,卡尔德蒙同工型表达和膀胱功能。进行了膀胱测压,十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和蛋白质印迹分析,以确定膀胱功能和收缩蛋白表达的变化。结果:总的来说,我们观察到膀胱重量与SM2与SM1之比具有显着相关性(p <0.05)。不管阻塞的持续时间(长达10周),该比率似乎都稳定在与胎儿兔平滑肌细胞相当的值附近,这表明SM2和SM1表达逆转至与胎儿阶段相似的水平。 h和l-caldesmon亚型的表达模式显示梗阻性膀胱中l-caldesmon的表达增加。除了阻塞组的泄漏点压力降低外,我们注意到膀胱容量或顺应性在统计学上没有明显的尿动力学变化。结论:最有名的梗阻标志物膀胱重量与SM2与SM1的比率存在显着相关性。肌球蛋白重链同工型表达比似乎是减轻膀胱出口梗阻前后膀胱平滑肌表型调节的指标。因此,它可用作膀胱功能障碍的标志物和功能恢复的预测指标。退缩至胎儿的蛋白质表达模式可能表明对平滑肌细胞的不可逆转的损害,可能限制了其恢复。

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