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Role of sialic acid in urinary cytoprotective activity of Tamm-Horsfall protein.

机译:唾液酸在Tamm-Horsfall蛋白对尿液细胞的保护作用中的作用。

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OBJECTIVES: Tamm-Horsfall protein (THP) from normal urine has been shown to protect against the cytotoxic effects of toxic urinary cations (TFs) in vivo and in vitro. This study investigated the effect of desialylation on the cytoprotective activity of THP. METHODS: From pooled 24-hour urine specimens from healthy individuals, both TFs and THP were obtained. Sprague-Dawley rats received intravesical NaCl or KCl, and the baseline urodynamic percentage of nonvoiding contractions (NVCs) was recorded. Then, rehydrated TF, TF plus THP, or TF plus THP-desialylated (THP-d) were instilled, followed by KCl, and the urodynamic measurements were repeated. In vitro, human HTB4 bladder cells were incubated overnight with the rehydrated TF, TF plus THP, TF plus THP-d, or assay media alone, and the cytotoxicity levels were determined. RESULTS: Acid hydrolysis resulted in an 88% loss of sialic acid. TFs consistently demonstrated a greater than 50% toxicity for human HTB4 cells compared with cells incubated in media (P<0.01). TF cytotoxic activity was blocked by preincubation with THP but not by preincubation with THP-d. Similarly, rat bladder NVCs increased significantly over baseline when KCl was infused after TF infusion (1.68 NVCs/min; P <0.0001). NVCs were significantly reduced by preincubating TFs with THP (0.42 NVCs/min) but not by preincubating with THP-d (1.55 NVCs/min, P <0.0001). CONCLUSIONS: The cytoprotective function of urinary THP in the bladder can be compromised when a decrease is present in the sialic acid residues on THP. Such a decrease in THP cytoprotective activity may play a critical role in the pathophysiology of interstitial cystitis.
机译:目的:正常尿液中的Tamm-Horsfall蛋白(THP)在体内和体外均能抵抗毒性尿阳离子(TFs)的细胞毒性作用。这项研究调查了脱唾液酸对THP的细胞保护活性的影响。方法:从健康个体收集的24小时尿液样本中,获得TFs和THP。 Sprague-Dawley大鼠接受膀胱内NaCl或KCl,并记录无尿收缩(NVC)的基线尿动力学百分比。然后,注入再水合的TF,TF加THP或TF加THP去甲酰化(THP-d),然后注入KCl,并重复进行尿流动力学测量。在体外,将人HTB4膀胱细胞与再水化的TF,TF加THP,TF加THP-d或单独的测定培养基孵育过夜,并测定细胞毒性水平。结果:酸水解导致唾液酸损失88%。与在培养基中温育的细胞相比,TF持续显示出对人类HTB4细胞具有大于50%的毒性(P <0.01)。通过与THP的预温育而不是通过与THP-d的预温育来阻断TF的细胞毒性活性。同样,TF输注后输注氯化钾后,大鼠膀胱NVC明显高于基线(1.68 NVC / min; P <0.0001)。通过将Tf与THP预温育(0.42 NVCs / min)可以显着降低NVC,而与THP-d(1.55 NVCs / min,P <0.0001)则不可以。结论:当THP上唾液酸残基减少时,尿THP在膀胱中的细胞保护功能可能受到损害。 THP细胞保护活性的这种降低可能在间质性膀胱炎的病理生理中起关键作用。

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