中国血液流变学杂志
中國血液流變學雜誌
중국혈액류변학잡지
CHINESE JOURNAL OF HEMORHEOLOGY
2013年
2期
207-210,225
,共5页
石小蕊%姜彧滕%邹士涛%倪建龙%高利平%徐徐%于美云%姜智%周迎会%吴士良
石小蕊%薑彧滕%鄒士濤%倪建龍%高利平%徐徐%于美雲%薑智%週迎會%吳士良
석소예%강욱등%추사도%예건룡%고리평%서서%우미운%강지%주영회%오사량
4IgB7-H3%转染%SW480%β3GnT8%多聚乳糖胺
4IgB7-H3%轉染%SW480%β3GnT8%多聚乳糖胺
4IgB7-H3%전염%SW480%β3GnT8%다취유당알
4IgB7-H3%transfection%SW480%β3GnT8%polylactosamine
目的探索人结肠癌细胞SW480转染4IgB7-H3后对糖基转移酶β3GnT8和细胞表面多聚乳糖胺糖链表达的影响。方法脂质体介导的重组表达载体pIRES2-EGFP/4IgB7-H3转染SW480细胞,筛选并获得稳定表达4IgB7-H3的亚克隆细胞株;RT-PCR、Western Blot检测β3GnT8的表达;流式细胞术检测多聚乳糖胺寡糖链的表达。结果成功获得稳定表达4IgB7-H3的亚克隆细胞株SW480/4IgB7-H3;转染4IgB7-H3的SW480细胞中β3GnT8和多聚乳糖胺糖链的表达均明显下调(P<0.05)。结论人肠癌细胞中4IgB7-H3过表达能抑制β3GnT8的表达,进而抑制多聚乳糖胺糖链的表达。
目的探索人結腸癌細胞SW480轉染4IgB7-H3後對糖基轉移酶β3GnT8和細胞錶麵多聚乳糖胺糖鏈錶達的影響。方法脂質體介導的重組錶達載體pIRES2-EGFP/4IgB7-H3轉染SW480細胞,篩選併穫得穩定錶達4IgB7-H3的亞剋隆細胞株;RT-PCR、Western Blot檢測β3GnT8的錶達;流式細胞術檢測多聚乳糖胺寡糖鏈的錶達。結果成功穫得穩定錶達4IgB7-H3的亞剋隆細胞株SW480/4IgB7-H3;轉染4IgB7-H3的SW480細胞中β3GnT8和多聚乳糖胺糖鏈的錶達均明顯下調(P<0.05)。結論人腸癌細胞中4IgB7-H3過錶達能抑製β3GnT8的錶達,進而抑製多聚乳糖胺糖鏈的錶達。
목적탐색인결장암세포SW480전염4IgB7-H3후대당기전이매β3GnT8화세포표면다취유당알당련표체적영향。방법지질체개도적중조표체재체pIRES2-EGFP/4IgB7-H3전염SW480세포,사선병획득은정표체4IgB7-H3적아극륭세포주;RT-PCR、Western Blot검측β3GnT8적표체;류식세포술검측다취유당알과당련적표체。결과성공획득은정표체4IgB7-H3적아극륭세포주SW480/4IgB7-H3;전염4IgB7-H3적SW480세포중β3GnT8화다취유당알당련적표체균명현하조(P<0.05)。결론인장암세포중4IgB7-H3과표체능억제β3GnT8적표체,진이억제다취유당알당련적표체。
Objective To explore the expressions of glycosyltransferaseβ3GnT8 and polylactosamine on cell surface in human colon cancer cell line SW480 transfected with 4IgB7-H3.Methods Liposome-mediated method transfected recombinant expression carrier pIRES2-EGFP/4IgB7-H3 into SW480 cells;RT-PCR,Western Blot detected the expression of 4IgB7-H3 andβ3GnT8 at the mRNA and protein levels;Flow cytometry detcted lactosamine oligosaccharide chain expression.Results 4IgB7-H3 recombinant expression vector was successfully constructed.Then stably transfected SW480 cell line was got.Both the expressions ofβ3GnT8 and poly lactose amine sugar chain decreased signiifcantly(P<0.05) after transfection.Conclusion 4IgB7-H3 overexpression in human colorectal cancer cells can inhibitβ3GnT8 production,and thereby inhibit poly galactosamine extension.