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李建達 間質性膀胱炎病患的膀胱上皮,其ROMK和KCNQ1 兩種鉀離子通道的表現不同 2017/7/3 上午 03:07:15 0
原 文 題  目 Differential Expression of Renal Outer Medullary K+ Channel and Voltage-gated K+ Channel 7.1 in Bladder Urothelium of Patients With Interstitial Cystitis/Painful Bladder Syndrome
作  者 Jane-Dar Lee (李建達), Ming-Huei Lee, Wen-Kai Yang, Kuan-Lin Wang, and Tsung-Han Lee
出  處 UROLOGY 101: 169.e1–169.e5, 2017.
出版日期 March, 2017.
評 論 評論:

研究目的:間質性膀胱炎的臨床症狀如急尿、頻尿、夜尿和膀胱疼痛等,學者Parsons CL認為是鉀離子滲透所造成;先前研究在膀胱上皮中有renal outer medullary K+ channel (ROMK) and voltage-gated K+ channel 7.1 (KCNQ1)兩種鉀離子通道蛋白,ROMK位於膀胱上皮細胞頂膜開口;KCNQ1則於細胞基底膜位置; 本實驗在探討間質性膀胱炎中,兩種不同位置的鉀離子通道所表現的情形。


材料與方法:

患有間質性膀胱炎的實驗組病人24個,及12個沒有任何IC/PBS症狀的自願者為對照組,分別利用膀胱鏡檢取得樣本。我們利用西方墨點法偵測其蛋白質表現量,及用免疫螢光染色和共軛焦顯微鏡來標定鉀離子通道蛋白在膀胱上皮的表現位置。數據結果利用Mann-Whitney U test做統計分析。


結果:

依據免疫組織化學染色及共軛焦顯微鏡發現,位於頂膜的鉀離子通道蛋白(ROMK)表現量顯著高於對照組3.3倍;但是位於基底膜的(KCNQ1)通道,兩組在統計上沒有顯著差異。


結論:

我們的實驗數據顯示,大量的ROMK蛋白表現在IC/PBS這組病人的膀胱上皮細胞的頂膜上;而位於膀胱上皮細胞的基底膜KCNQ1鉀離子通道,兩組並沒有顯著差異;這結果讓我們推測IC/PBS的病人利用膀胱上皮細胞頂膜上的ROMK鉀離子通道,極力讓滲入的鉀離子流回膀胱內腔,以維護異常上皮細胞內鉀離子的衡定。
abstract

摘要:
OBJECTIVE: To investigate the changes including expression and localization of 2 potassium channels, renal outer medullary K+ channel (ROMK) and voltage-gated K+ channel 7.1 (KCNQ1), after increased urinary potassium leakage in patients with interstitial cystitis/painful bladder syndrome (IC/PBS).

MATERIALS AND METHODS:
The study group included 24 patients with IC/PBS and a control group consisting of 12 volunteers without any IC/PBS symptoms. Bladder biopsies were taken from both groups. We determined the protein expression and distribution of potassium channels using immunoblotting, immunohistochemistry, and immunofluorescent staining under confocal laser microscopy.

RESULTS:
The results revealed that ROMK was predominantly expressed in apical cells of the bladder urothelium at significantly higher levels (3.3-fold) in the study group than in the control group. In contrast, KCNQ1 was expressed in the basolateral membrane according to confocal microscopy results and did not significantly differ between groups.

CONCLUSION:
Our data showed that the abundance of ROMK protein in apical cells was increased in the IC/PBS group, whereas KCNQ1, which was distributed in the basolateral membrane of the bladder urothelium, showed similar abundance between groups. These results suggest that upregulation of the ROMK channel in apical cells might permit avid potassium flux into the bladder lumen to maintain intracellular K+ homeostasis in the dysfunctional urothelium.

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