• 1.杭州市蕭山區(qū)第一人民醫(yī)院普通外科(杭州311201);;
  • 2.瀘州醫(yī)學(xué)院附屬醫(yī)院肝膽外科(四川瀘州646000);;
  • 3.瀘州醫(yī)學(xué)院附屬醫(yī)院病理科;

目的研究不同類型(囊狀、梭狀型)先天性膽總管囊腫壁細(xì)胞凋亡與增殖的關(guān)系,了解細(xì)胞凋亡/增殖在膽總管囊腫中的作用。方法以膽總管囊狀擴(kuò)張組32例、梭狀擴(kuò)張組35例及膽總管結(jié)石致膽管擴(kuò)張組(對(duì)照組)25例為研究對(duì)象。術(shù)中取部分膽總管壁送檢,觀察膽總管壁損傷情況。用免疫組織化學(xué)法檢測(cè)細(xì)胞凋亡的相關(guān)指標(biāo)bcl2、bax及細(xì)胞增殖指標(biāo)PCNA的表達(dá); 用TUNEL法檢測(cè)細(xì)胞凋亡情況。結(jié)果囊狀擴(kuò)張組膽總管壁粘膜上皮細(xì)胞破壞嚴(yán)重,梭狀擴(kuò)張組鏡下所見(jiàn)與囊狀擴(kuò)張組相似,但程度較輕。對(duì)照組膽總管粘膜上皮細(xì)胞破壞最輕,其凋亡細(xì)胞呈散在分布,上皮細(xì)胞和成纖維細(xì)胞凋亡陽(yáng)性率較低,分別為(2.74±1.00)%和(2.95±0.87)%; bcl2、bax表達(dá)率較低,水平相似(P gt;0.05); PCNA表達(dá)率較高,分別為(3.74±1.00)%和(3.71±1.77)%。囊狀擴(kuò)張組與梭狀擴(kuò)張組囊壁殘留上皮中的bcl2和PCNA表達(dá)率低,分別為(0.99±0.51)%和(0.90±0.38)%; bax呈高表達(dá),bcl2呈低表達(dá),凋亡細(xì)胞陽(yáng)性率較高,分別為(13.94±4.77)%和(7.51±3.46)%; 成纖維細(xì)胞中的PCNA表達(dá)率較高,分別為(9.91±2.91)%和(9.70±3.18)%,bax呈低表達(dá),bcl2呈高表達(dá),凋亡細(xì)胞陽(yáng)性率較低,分別為(3.74±2.12)%和(4.46±2.41)%。兩組之間上述各項(xiàng)指標(biāo)比較無(wú)明顯差異(P gt;0.05),但兩組的bcl2和bax的表達(dá)與對(duì)照組比較則明顯升高(P<0.05)。結(jié)論細(xì)胞凋亡在膽總管囊腫形成中有一定的促進(jìn)作用。

引用本文: 張愛(ài)民,雷正明,黎靖,植勇,龍漢安. 細(xì)胞凋亡與增殖在先天性膽總管囊腫發(fā)病中的作用. 中國(guó)普外基礎(chǔ)與臨床雜志, 2003, 10(1): 43-45. doi: 復(fù)制

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  1. 1. 曾思務(wù),劉雨,梁粉花,等. 膽囊病變時(shí)bcl2和p16蛋白產(chǎn)物的表達(dá)和意義 [J]. 中國(guó)普外基礎(chǔ)與臨床雜志, 1999; 6(2)∶26.
  2. 2. 劉戰(zhàn)培,嚴(yán)律南. bcl蛋白在肝細(xì)胞肝癌發(fā)生過(guò)程中的表達(dá)及其與肝細(xì)胞凋亡變化的關(guān)系 [J]. 中國(guó)普外基礎(chǔ)與臨床雜志, 1999; 6(4)∶193.
  3. 3. 徐宏勇,李開(kāi)宗,付由池,等. 人肝細(xì)胞癌中促凋亡基因bax的原位檢測(cè)及其臨床意義 [J]. 中國(guó)普外基礎(chǔ)與臨床雜志, 2000; 7(4)∶238.
  4. 4. 陳肖鳴,李仲榮,劉平. 近10年小兒膽總管囊腫診治變遷(附79例報(bào)告) [J]. 中國(guó)普外基礎(chǔ)與臨床雜志, 1999; 6(3)∶90.
  5. 5. Todani T, Watanabe Y, Narusue M, et al. Congenital bile duct cysts: classification,operative procedures,and review of thirtyseven cases including cancer arising from choledochal cyst [J]. Am J Surg, 1977; 134(2)∶263.
  6. 6. Todani T,Watanabe Y,F(xiàn)ujii T, et al.Congenital choledochal cyst with intrahepatic involvement [J]. Arch Surg,1984; 119(9)∶1038.
  7. 7. 肖現(xiàn)民,周以明,陳蓮,等. 囊形和梭形擴(kuò)張癥的比較觀察和病因探討 [J]. 肝膽外科雜志, 1998; 6(4)∶200.
  8. 8. Oltvai ZN,Milliman CL,Korsmeyer ST. Bcl2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death [J]. Cell, 1993; 74(4)∶609.
  9. 9. Wyllie AH. Apoptosis. Death gets a brake [J]. Nature, 1994; 369(6478)∶272.
  10. 10. Miyano T,Suruga K,Suda K.Abnormal choledochopancreatico ductal junction related to the etiology of infantile obstructive jaundice disease [J]. J Pediatr Surg, 1979; 14(1)∶16.
  11. 11. Hall PA, Levison DA,Woods AL, et al. Proliferating cell nuclear antigen(PCNA) immunolocalization in paraffin sections: an index of cell proliferation with evidence of deregulated expression in some neoplasms [J]. J Pathol, 1990; 162(4)∶285.
  12. 12. Jacobson MD,Burne JF,King MP, et al.Bcl2 blocks apoptosis in cells lacking mitochondrial DNA [J]. Nature, 1993; 361(6410)∶365.
  13. 13. 曾昭惠,杜瓊,楊明清. 自由基氧化致線粒體DNA損傷與細(xì)胞凋亡 [J]. 國(guó)外醫(yī)學(xué)臨床生化與檢驗(yàn)學(xué)分冊(cè), 1999; 20(4)∶167.
  14. 14. Li P,Nijhawan D,Budihardjo I, et al.Cytochrome c and dATPdependent formation of Apaf1/caspase9 complex initiates an apoptotic protease cascade [J]. Cell, 1997; 91(4)∶479.
  15. 15. Naga S. Apoptosis by death factor [J]. Cell, 1997; 88(3)∶355.