中国现代医学杂志
中國現代醫學雜誌
중국현대의학잡지
CHINA JOURNAL OF MODERN MEDICINE
2008年
1期
8-12,20
,共6页
白菡%何丽霞%张琳%冯国和%石理兰%窦晓光%赵桂珍
白菡%何麗霞%張琳%馮國和%石理蘭%竇曉光%趙桂珍
백함%하려하%장림%풍국화%석리란%두효광%조계진
乙型肝炎病毒%滋养层细胞%宫内传播%感染%凋亡
乙型肝炎病毒%滋養層細胞%宮內傳播%感染%凋亡
을형간염병독%자양층세포%궁내전파%감염%조망
hepatitis B virus%trophoblastic cells%intrauterine transmission%infection%apoptosis
目的 检测HBV感染后人绒毛膜滋养层细胞的HBV标志物的表达和细胞的形态学变化,探讨HBV对滋养层细胞的感染与HBV宫内传播的关系.方法 将HBV感染的血清与原代培养的人早孕绒毛膜滋养层细胞及传代细胞JEG-3共同孵育8~48 h,通过倒置显微镜观察细胞的形态及细胞间连接,细胞免疫荧光方法 检测滋养层细胞中HBsAg的表达,荧光定量PCR方法 检测细胞中的HBV DNA,TUNEL方法 检测滋养层细胞的凋亡.结果 滋养层细胞与HBV感染的血清共同孵育后,滋养层细胞的形态及细胞间连接无明显变化;但通过免疫荧光方法 检测到滋养层细胞中HBsAg的阳性表达,并通过荧光定量PCR方法 检测到滋养层细胞中HBV DNA的存在;同时,细胞凋亡检测结果表明,与HBV感染的血清共同孵育后,滋养层细胞的凋亡数量明显增加.结论 HBV可以感染体外培养的滋养层细胞;HBV感染可以诱导滋养层细胞凋亡,滋养层细胞的感染和凋亡可能与HBV的宫内传播机制有关.
目的 檢測HBV感染後人絨毛膜滋養層細胞的HBV標誌物的錶達和細胞的形態學變化,探討HBV對滋養層細胞的感染與HBV宮內傳播的關繫.方法 將HBV感染的血清與原代培養的人早孕絨毛膜滋養層細胞及傳代細胞JEG-3共同孵育8~48 h,通過倒置顯微鏡觀察細胞的形態及細胞間連接,細胞免疫熒光方法 檢測滋養層細胞中HBsAg的錶達,熒光定量PCR方法 檢測細胞中的HBV DNA,TUNEL方法 檢測滋養層細胞的凋亡.結果 滋養層細胞與HBV感染的血清共同孵育後,滋養層細胞的形態及細胞間連接無明顯變化;但通過免疫熒光方法 檢測到滋養層細胞中HBsAg的暘性錶達,併通過熒光定量PCR方法 檢測到滋養層細胞中HBV DNA的存在;同時,細胞凋亡檢測結果錶明,與HBV感染的血清共同孵育後,滋養層細胞的凋亡數量明顯增加.結論 HBV可以感染體外培養的滋養層細胞;HBV感染可以誘導滋養層細胞凋亡,滋養層細胞的感染和凋亡可能與HBV的宮內傳播機製有關.
목적 검측HBV감염후인융모막자양층세포적HBV표지물적표체화세포적형태학변화,탐토HBV대자양층세포적감염여HBV궁내전파적관계.방법 장HBV감염적혈청여원대배양적인조잉융모막자양층세포급전대세포JEG-3공동부육8~48 h,통과도치현미경관찰세포적형태급세포간련접,세포면역형광방법 검측자양층세포중HBsAg적표체,형광정량PCR방법 검측세포중적HBV DNA,TUNEL방법 검측자양층세포적조망.결과 자양층세포여HBV감염적혈청공동부육후,자양층세포적형태급세포간련접무명현변화;단통과면역형광방법 검측도자양층세포중HBsAg적양성표체,병통과형광정량PCR방법 검측도자양층세포중HBV DNA적존재;동시,세포조망검측결과표명,여HBV감염적혈청공동부육후,자양층세포적조망수량명현증가.결론 HBV가이감염체외배양적자양층세포;HBV감염가이유도자양층세포조망,자양층세포적감염화조망가능여HBV적궁내전파궤제유관.
[Objective] To investigate on the relationship between trophoblastic cells infection and intrauterine transmission of HBV, the HBV markers and cell morphology of troplastic cells after being infected with HBV were detected. [Methods] The serum containing HBV was cocultured with the primary cultured trophoblastic cells and JEG-3 cell line for 8 to 48 hours. The appearance of the cells and cell-cell conjunction were observed by inverted microscope. HBsAg in the cells was detected by cell immunofluorescence. Fluorescent quantitation-PCR was used to detect HBV DNA in the culture cells. And TUNEL technique was used to detect the cell apoptosis. [Results] After co-infection with the HBV positive serum, the appearance of the trophoblastic cells and cell-cell conjunction were not markedly changed; but the results of cell immunofluorescence showed that HBsAg could be detected in the cells.HBV DNA was detected by fluorescent quantitation-PCR. And the TUNEL results showed that the cell apoptosis increased after the co-infection. [Conclusion] In vitro cultured trophoblastic cells can be infected by HBV. Infection of HBV may induce the apoptosis of the trophoblastic cells. Apoptosis and infection of trophoblastic cells may be related with the mechanism of HBV intrauterine transmission.