中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2014年
9期
1933-1935
,共3页
李常海%廖铂%王艳军%董为%董汉华%梁慧芳%陈孝平
李常海%廖鉑%王豔軍%董為%董漢華%樑慧芳%陳孝平
리상해%료박%왕염군%동위%동한화%량혜방%진효평
肝卵圆细胞%肝肿瘤%乙肝病毒%黄曲霉素
肝卵圓細胞%肝腫瘤%乙肝病毒%黃麯黴素
간란원세포%간종류%을간병독%황곡매소
Hepatic oval cell strain%Liver tumor%Hepatitis B virus%Aflatoxin B1
目的 研究体内微环境对肝卵圆细胞分化的影响,探讨肝卵圆细胞是否可在体内分化为肝癌.方法 在使用黄曲霉素作为诱癌剂的情况下,将转染乙肝病毒X基因(HBx)的大鼠卵圆细胞种植于裸鼠皮下,形成肿瘤后再移植至同一裸鼠肝实质内,使其继续生长.收集皮下肿瘤和肝内肿瘤,用苏木素-伊红(HE)、免疫组织化学染色和透射电镜对其进行检查,明确其性质.结果 10周时,实验组中10只(10/15)裸鼠形成皮下肿瘤,对照组中8只(8/15)裸鼠形成皮下肿瘤,两组在肿瘤大小和生长速度方面差异无统计学意义(P>0.05);两组均在皮下分化成间质肿瘤,表达间质性标志物波形蛋白(Vimentin)和平滑肌肌动蛋白(SMA).皮下间质肿瘤移植至肝内8周后,在肝内种植处长成肝内肿瘤;经病理确诊实验组肿瘤为肝癌肉瘤(由恶性间质细胞和肝癌细胞组成),表达HepPar1、细胞角蛋白8(CK8)和甲胎蛋白(AFP)抗原,说明肝卵圆细胞在HBx和黄曲霉素的共同作用下可部分分化成肝细胞癌.结论 肝卵圆细胞具有可塑性,局部微环境对其分化方向起关键作用;肝癌可能来源于卵圆细胞的异常分化.
目的 研究體內微環境對肝卵圓細胞分化的影響,探討肝卵圓細胞是否可在體內分化為肝癌.方法 在使用黃麯黴素作為誘癌劑的情況下,將轉染乙肝病毒X基因(HBx)的大鼠卵圓細胞種植于裸鼠皮下,形成腫瘤後再移植至同一裸鼠肝實質內,使其繼續生長.收集皮下腫瘤和肝內腫瘤,用囌木素-伊紅(HE)、免疫組織化學染色和透射電鏡對其進行檢查,明確其性質.結果 10週時,實驗組中10隻(10/15)裸鼠形成皮下腫瘤,對照組中8隻(8/15)裸鼠形成皮下腫瘤,兩組在腫瘤大小和生長速度方麵差異無統計學意義(P>0.05);兩組均在皮下分化成間質腫瘤,錶達間質性標誌物波形蛋白(Vimentin)和平滑肌肌動蛋白(SMA).皮下間質腫瘤移植至肝內8週後,在肝內種植處長成肝內腫瘤;經病理確診實驗組腫瘤為肝癌肉瘤(由噁性間質細胞和肝癌細胞組成),錶達HepPar1、細胞角蛋白8(CK8)和甲胎蛋白(AFP)抗原,說明肝卵圓細胞在HBx和黃麯黴素的共同作用下可部分分化成肝細胞癌.結論 肝卵圓細胞具有可塑性,跼部微環境對其分化方嚮起關鍵作用;肝癌可能來源于卵圓細胞的異常分化.
목적 연구체내미배경대간란원세포분화적영향,탐토간란원세포시부가재체내분화위간암.방법 재사용황곡매소작위유암제적정황하,장전염을간병독X기인(HBx)적대서란원세포충식우라서피하,형성종류후재이식지동일라서간실질내,사기계속생장.수집피하종류화간내종류,용소목소-이홍(HE)、면역조직화학염색화투사전경대기진행검사,명학기성질.결과 10주시,실험조중10지(10/15)라서형성피하종류,대조조중8지(8/15)라서형성피하종류,량조재종류대소화생장속도방면차이무통계학의의(P>0.05);량조균재피하분화성간질종류,표체간질성표지물파형단백(Vimentin)화평활기기동단백(SMA).피하간질종류이식지간내8주후,재간내충식처장성간내종류;경병리학진실험조종류위간암육류(유악성간질세포화간암세포조성),표체HepPar1、세포각단백8(CK8)화갑태단백(AFP)항원,설명간란원세포재HBx화황곡매소적공동작용하가부분분화성간세포암.결론 간란원세포구유가소성,국부미배경대기분화방향기관건작용;간암가능래원우란원세포적이상분화.
Objective To study the role of microenvironment on the differentiation of hepatic oval cells and explore whether hepatic oval cells can differentiate into liver cancer.Methods The transfected hepatitis B virus X oncogene (HBx) rat hepatic oval cells were implanted into the subcutaneous tissue of nude mice to develop tumor for 10 weeks,then the subcutaneous tumors were collected and divided to transplant into liver parenchyma,at the same time treating with aflatoxin B1 (AFB1) for 18 weeks.The subcutaneous tumors and intrahepatic tumors were collected and stained by haematoxylin and eosin (HE) and immunohistochemistry staining,as well as observed by transmission electron microscopy.Results About 10 weeks,10 (10/15) subcutaneous tumor formation in group A and 8 (8/15) subcutaneous tumor formation in control group.The subcutaneous tumors were composited by the mesenchymal cells with expression of mesenchymal marker Vimentin and smooth muscle actin (SMA).8 weeks after transplantation,the intrahepatic tumors were found at the site of inoculated.The HBx intrahepatic tumor included components of mesenchymal cells,which expressing Vimentin and SMA,and cancer cells,which accounting for about 10%-20% of cells and expressed HepParl,cytokeratin 8 (CK8),and alpha fetal protein (AFP) antigen.These results indicate that the intrahepatic tumor was liver carcinosarcoma and oval cells can be abnormal differentiated into hepatocellular carcinoma on the cooperation of the HBx gene and AFB1.Conclusion Hepatic oval cells have the plasticity and local microenvironment play a key role on its differentiation ; hepatocellular carcinoma is likely to come from the abnormal differentiation of oval cells.