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首页> 外文期刊>Open Journal of Urology >Expression of Large Conductance, Voltage- and Ca2+-Activated K+ (BK) Channels in Human Urinary Bladder: Alteration of Subunit Expression Profile in Association with Bladder Outlet Obstruction
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Expression of Large Conductance, Voltage- and Ca2+-Activated K+ (BK) Channels in Human Urinary Bladder: Alteration of Subunit Expression Profile in Association with Bladder Outlet Obstruction

机译:大电导,电压和Ca 2 +激活的K +(BK)通道在人类膀胱中的表达:与膀胱出口梗阻相关的亚基表达谱的变化。

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Purpose: Large conductance, voltage- and Ca2+-activated K+ (BK) channel is thought to have a central role to regulate urinary bladder smooth muscle functions, and its dysfunction may lead to increase of urination frequency and overactive bladder. The present study aims to investigate the expression pattern of BK channel subunits in the human urinary bladder, and how it changes in association with bladder outlet obstruction (BOO). Materials and Methods: Human bladders were obtained from 7 controls without prostatic enlargement and lower urinary tract symptoms and 4 BPH patients with clinically diagnosed overactive bladder who were verified by the International Prostate Symptom Score (IPSS) and prostate volume. The expression and location of BK channel protein complex was examined using immunohistochemistry with affinity-purified anti-BKα antibodies. A real-time RT-PCR was used to quantify the expression of each BK channel subunit (α and β1 - 4) gene in the mucosal and muscle layers of human urinary bladder. Results: Immunohistochemical staining for BK-α protein complex was localized in the muscle and submucosal regions of urinary bladder. RT-PCR analysis revealed the presence of α-, β1-, and β4-subunit genes of BK channel in the mucosal layer, α- and β1-subunit in the muscle layer. The expressions of α- and β1-subunit genes in the muscle (α: p = 0.0003, β1: p = 0.0003) and mucosal (α: p = 0.03, β1: p = 0.02) layers significantly decreased in BOO bladders compared with controls. The expression levels of α- and β1-subunit in mucosal layer were statistically correlated with storage score of IPSS (α; r = 0.84, p = 0.002, β1; r = 0.84, p = 0.002), and so were in muscle layer (α; r = 0.934, p 0.0001, β1; r = 0.917, p = 0.00018). Conclusions: BK channels, which are mainly composed of α- and β1-subunits, are expressed in both the mucosal and muscle layers of human urinary bladder. Decreased expression of BK channel in BOO might be implicated in the mechanisms underlying the development of overactive bladder.
机译:目的:大电导,电压激活和Ca2 +激活的K +(BK)通道被认为在调节膀胱平滑肌功能中起着中心作用,其功能障碍可能导致排尿频率增加和膀胱过度活跃。本研究旨在调查人膀胱中BK通道亚基的表达模式,以及其如何与膀胱出口梗阻(BOO)相关联地变化。材料和方法:从7个无前列腺肿大和下尿路症状的对照组和4例经临床诊断为膀胱过度活动症的BPH患者(经国际前列腺症状评分(IPSS)和前列腺体积验证)获得人膀胱。使用亲和纯化的抗BKα抗体的免疫组织化学检查了BK通道蛋白复合物的表达和位置。实时RT-PCR用于定量人膀胱膀胱粘膜和肌肉层中每个BK通道亚基(α和β1-4)基因的表达。结果:BK-α蛋白复合物的免疫组织化学染色位于膀胱的肌肉和粘膜下区域。 RT-PCR分析显示在粘膜层存在BK通道的α-,β1-和β4-亚基基因,在肌肉层中存在α-和β1-亚基。与对照组相比,BOO膀胱中肌肉(α:p = 0.0003,β1:p = 0.0003)和粘膜(α:p = 0.03,β1:p = 0.02)层中α-和β1-亚基基因的表达显着降低。 。粘膜层中α-和β1-亚基的表达水平与IPSS的存储评分呈统计学相关性(α; r = 0.84,p = 0.002,β1; r = 0.84,p = 0.002),而在肌肉层中也是如此( α; r = 0.934,p = 0.0001,β1; r ​​= 0.917,p = 0.00018)。结论:BK通道主要由α-和β1-亚基组成,在人膀胱的粘膜层和肌肉层均有表达。 BOO中BK通道表达的减少可能与膀胱过度活动症的潜在发病机制有关。

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