Guo Wan-liang, Zhang Qi, Wang Jian, Jin Mei-fang
Radiology Department, Children's Hospital Affiliated to Soochow University, Suzhou, China.
Pediatr Surg Int. 2013 Mar;29(3):293-8. doi: 10.1007/s00383-012-3225-0. Epub 2012 Dec 9.
To examine the content of phosphorylated myosin regulatory light chain (P-MLC20) and myosin light-chain kinase (MLCK) in the common bile duct of pediatric patients with pancreaticobiliary maljunction (PBM) accompanied by bile duct dilatation (BDD), and investigate their potential role in PBM accompanied by BDD.
Twenty-one specimens of the common bile duct from pediatric patients with PBM accompanied by BDD were collected. P-MLC20 was examined with immunohistochemistry. The expression of P-MLC20 and MLCK was also examined with Western blot. Twenty-one specimens of the common bile duct from pediatric patients without PBM and BDD were used as controls.
The mean optical density (MOD), mean labeling intensity (MLI) and minimum qualifying scores (MQS) of P-MLC20 were 115.6856 ± 58.1634, 21.7125 % ± 9.6555 and 21.3531 ± 6.5255, respectively. In the control group, MOD, MLI and MQS were 96.5581 ± 9.7859, 11.1813 % ± 3.6208 and 10.7819 ± 3.5323, respectively. There was no significant difference in MOD between the two groups (P > 0.05), whereas there was a significant difference in MLI and MQS between the two groups (P < 0.05). The expression of P-MLC20 and MLCK, as determined with Western blot, was also significantly higher in the PBM group than in the control group (P < 0.05).
P-MLC20 is associated with increased contractile force of the smooth muscle of the common bile duct in pediatric patients with PBM accompanied by BDD. The enhanced expression of P-MLC20 in the common bile duct probably contributes to increased bile duct pressure in PBM via the MLCK pathway.
检测胰胆管合流异常(PBM)伴胆管扩张(BDD)患儿胆总管中磷酸化肌球蛋白调节轻链(P-MLC20)和肌球蛋白轻链激酶(MLCK)的含量,探讨其在PBM伴BDD中的潜在作用。
收集21例PBM伴BDD患儿的胆总管标本。采用免疫组织化学法检测P-MLC20。同时采用蛋白质免疫印迹法检测P-MLC20和MLCK的表达。选取21例无PBM及BDD的患儿胆总管标本作为对照。
P-MLC20的平均光密度(MOD)、平均标记强度(MLI)和最小合格分数(MQS)分别为115.6856±58.1634、21.7125%±9.6555和21.3531±6.5255。对照组的MOD、MLI和MQS分别为96.5581±9.7859、11.1813%±3.6208和10.7819±3.5323。两组MOD差异无统计学意义(P>0.05),而MLI和MQS差异有统计学意义(P<0.05)。蛋白质免疫印迹法检测结果显示,PBM组P-MLC20和MLCK的表达也显著高于对照组(P<0.05)。
P-MLC20与PBM伴BDD患儿胆总管平滑肌收缩力增强有关。胆总管中P-MLC20表达增强可能通过MLCK途径导致PBM时胆管压力升高。