安徽医药
安徽醫藥
안휘의약
ANHUI MEDICAL AND PHARMACEUTICAL JOURNAL
2015年
2期
276-279
,共4页
金亮%张茜%沙泉
金亮%張茜%沙泉
금량%장천%사천
结核分枝杆菌%人AB型血清%胎牛血清%外周血单个核细胞
結覈分枝桿菌%人AB型血清%胎牛血清%外週血單箇覈細胞
결핵분지간균%인AB형혈청%태우혈청%외주혈단개핵세포
mycobacterium tuberculosis%AB type of human serum%fetal bovine serum%PBMC
目的:观察添加人AB型血清或胎牛血清(FBS)培养基培养的人外周血单个核细胞(PBMC)在结核杆菌(M.tb)全菌裂解物( WCL)的刺激下增殖差异。方法健康成人PBMC 1×109· L-1,分别加入WCL 20 mg· L-1,或者同时给予人重组白细胞介素-2(rhIL-2)50 U· mL-1,植物血凝素(PHA)5 mg· L-1,同时设置空白对照组。分别在含10%人AB型血清的RP-MI1640培养液和10%FBS的RPMIl640培养液中培养6 d后,用倒置显微镜观察培养结果,运用流式细胞术检测淋巴细胞增殖情况。结果添加人AB型血清培养基培养条件下,M.tb WCL对淋巴细胞增殖效果较同样条件下添加FBS培养的增殖效果明显,差异有统计学意义( P<0.05)。在WCL和rhIL-2混合组中同样是添加人AB型血清培养增殖效果明显,差异有统计学意义( P<0.05)。结论当以M.tb WCL为抗原的刺激人PBMC时,淋巴细胞在添加人AB型血清培养液中比在添加FBS的培养液中增殖效果更加明显。
目的:觀察添加人AB型血清或胎牛血清(FBS)培養基培養的人外週血單箇覈細胞(PBMC)在結覈桿菌(M.tb)全菌裂解物( WCL)的刺激下增殖差異。方法健康成人PBMC 1×109· L-1,分彆加入WCL 20 mg· L-1,或者同時給予人重組白細胞介素-2(rhIL-2)50 U· mL-1,植物血凝素(PHA)5 mg· L-1,同時設置空白對照組。分彆在含10%人AB型血清的RP-MI1640培養液和10%FBS的RPMIl640培養液中培養6 d後,用倒置顯微鏡觀察培養結果,運用流式細胞術檢測淋巴細胞增殖情況。結果添加人AB型血清培養基培養條件下,M.tb WCL對淋巴細胞增殖效果較同樣條件下添加FBS培養的增殖效果明顯,差異有統計學意義( P<0.05)。在WCL和rhIL-2混閤組中同樣是添加人AB型血清培養增殖效果明顯,差異有統計學意義( P<0.05)。結論噹以M.tb WCL為抗原的刺激人PBMC時,淋巴細胞在添加人AB型血清培養液中比在添加FBS的培養液中增殖效果更加明顯。
목적:관찰첨가인AB형혈청혹태우혈청(FBS)배양기배양적인외주혈단개핵세포(PBMC)재결핵간균(M.tb)전균렬해물( WCL)적자격하증식차이。방법건강성인PBMC 1×109· L-1,분별가입WCL 20 mg· L-1,혹자동시급여인중조백세포개소-2(rhIL-2)50 U· mL-1,식물혈응소(PHA)5 mg· L-1,동시설치공백대조조。분별재함10%인AB형혈청적RP-MI1640배양액화10%FBS적RPMIl640배양액중배양6 d후,용도치현미경관찰배양결과,운용류식세포술검측림파세포증식정황。결과첨가인AB형혈청배양기배양조건하,M.tb WCL대림파세포증식효과교동양조건하첨가FBS배양적증식효과명현,차이유통계학의의( P<0.05)。재WCL화rhIL-2혼합조중동양시첨가인AB형혈청배양증식효과명현,차이유통계학의의( P<0.05)。결론당이M.tb WCL위항원적자격인PBMC시,림파세포재첨가인AB형혈청배양액중비재첨가FBS적배양액중증식효과경가명현。
Objective To observe the proliferation difference of human peripheral blood mononucelear cells ( PBMCs) which were stim-ulated with Mycobacterium tuberculosis ( M.tb) Whole Cell Lysate ( WCL) in human AB serum cell culture medium and fatal bovine serum ( FBS) cell culture medium.Methods PBMCs from healthy adults were stimulated by WCL or WCL with recombinant human interleukin 2 ( rhIL-2) or phytohemagglutinin ( PHA) or none as control in four groups.Each of the groups was cultured with RPMI-1640 medium containing 10%AB serum or 10%FBS for six days respectively.The proliferation of lymphocytes was carefully investiga-ted under the inverted microscope and flow cytometry.Results The proliferation of lymphocytes stimulated by WCL in medium with 10%AB serum is better than that in medium with 10%FBS (P<0.05).Similar results were obtained when PBMCs were stimulated by WCL and rhIL-2 (P<0.05) .Conclusion When human PBMCs were stimulated with M.tb WCL,the proliferation of lymphocytes was better in the culture medium supplemented with human AB serum than in that with FBS serum.