解放军医药杂志
解放軍醫藥雜誌
해방군의약잡지
MEDICAL&PHARMACEUTICAL JOURNAL OF CHINESE PEOPLE'S LIBERATION ARMY
2014年
7期
39-42
,共4页
樊红艳%哈小琴%张尚弟%杨志华%宋月娟%李晓云%刘延彤%徐越斌%林静
樊紅豔%哈小琴%張尚弟%楊誌華%宋月娟%李曉雲%劉延彤%徐越斌%林靜
번홍염%합소금%장상제%양지화%송월연%리효운%류연동%서월빈%림정
白细胞介素 2%沙门菌菌苗%疫苗,减毒%基因%血管抑制素类
白細胞介素 2%沙門菌菌苗%疫苗,減毒%基因%血管抑製素類
백세포개소 2%사문균균묘%역묘,감독%기인%혈관억제소류
Interleukin-2%Salmonella vaccines%Vaccine,attenuated%Gene%Angiostatins
目的:研究重组减毒沙门菌菌株 TPIN 对 HepG2细胞生物学性能的影响。方法 TPIN 转染 HepG2细胞36 h 时收集细胞表达上清,MTT 法检测表达产物对 HepG2细胞生长的作用;Transwell 迁移实验观察 TPIN 表达产物对 HepG2细胞迁移的影响;将不同剂量表达产物分别加入甲基纤维素小碟,并将小碟小心放入鸡胚绒毛尿囊膜,37.8℃继续孵化3 d,观察 IL-2/ NK4表达产物体外对鸡胚绒膜尿囊膜血管的效应。结果 TPIN 表达上清显著抑制HepG2细胞增殖的活性,且有一定剂量依赖效应;表达产物可明显抑制肿瘤细胞迁移,且明显抑制鸡胚绒膜尿囊膜血管形成。结论 TPIN 在体外能高效转染肿瘤细胞,表达目的蛋白 IL-2及 NK4,且表达产物能够抑制 HepG2细胞的增殖和迁移,对鸡胚绒膜尿囊膜血管的形成有抑制效应。
目的:研究重組減毒沙門菌菌株 TPIN 對 HepG2細胞生物學性能的影響。方法 TPIN 轉染 HepG2細胞36 h 時收集細胞錶達上清,MTT 法檢測錶達產物對 HepG2細胞生長的作用;Transwell 遷移實驗觀察 TPIN 錶達產物對 HepG2細胞遷移的影響;將不同劑量錶達產物分彆加入甲基纖維素小碟,併將小碟小心放入鷄胚絨毛尿囊膜,37.8℃繼續孵化3 d,觀察 IL-2/ NK4錶達產物體外對鷄胚絨膜尿囊膜血管的效應。結果 TPIN 錶達上清顯著抑製HepG2細胞增殖的活性,且有一定劑量依賴效應;錶達產物可明顯抑製腫瘤細胞遷移,且明顯抑製鷄胚絨膜尿囊膜血管形成。結論 TPIN 在體外能高效轉染腫瘤細胞,錶達目的蛋白 IL-2及 NK4,且錶達產物能夠抑製 HepG2細胞的增殖和遷移,對鷄胚絨膜尿囊膜血管的形成有抑製效應。
목적:연구중조감독사문균균주 TPIN 대 HepG2세포생물학성능적영향。방법 TPIN 전염 HepG2세포36 h 시수집세포표체상청,MTT 법검측표체산물대 HepG2세포생장적작용;Transwell 천이실험관찰 TPIN 표체산물대 HepG2세포천이적영향;장불동제량표체산물분별가입갑기섬유소소설,병장소설소심방입계배융모뇨낭막,37.8℃계속부화3 d,관찰 IL-2/ NK4표체산물체외대계배융막뇨낭막혈관적효응。결과 TPIN 표체상청현저억제HepG2세포증식적활성,차유일정제량의뢰효응;표체산물가명현억제종류세포천이,차명현억제계배융막뇨낭막혈관형성。결론 TPIN 재체외능고효전염종류세포,표체목적단백 IL-2급 NK4,차표체산물능구억제 HepG2세포적증식화천이,대계배융막뇨낭막혈관적형성유억제효응。
Objective To study the effect of an recombinant of attenuated Salmonella typhimurium strain (TPIN) on cytobiology characteristics of HepG2 hepatoma carcinoma cells. Methods Cultured supernatant was collect-ed from TPIN-transfected HepG2 cells for 36 h, and the effect of expression products on HepG2 cell growth was detected by MTT assay; the effect of TPIN expression products on HepG2 cell migration was assessed by Transwell method; differ-ent dosages of expression products were put on the Methylcellulose small plates, and then the small plates were put into chick chorioallantoic membrane and was hatched at 37. 8℃ for 3 d, and then angiogenic effect of different dosages of IL-2 / NK4 expression products on chick embryo was observed. Results Supernatant collected from TPIN-transfected cells significantly inhibited the activity of HepG2 cell multiplioation with a certain dose-dependent effect; expression products significantly inhibited the cell migration as well as the angiogenesis in chick chorioallantoic membrane. Conclusion TPIN can effectively transfect HepG2 cells in vitro and express IL2 and NK4 stably, and expression products can inhibit HepG2 proliferation and migration as well as the angiogenesis inhibition of chick chorioallantoic membrane.