中国实验动物学报
中國實驗動物學報
중국실험동물학보
ACTA LABORATORIUM ANIMALIS SCIENTIA SINICA
2014年
4期
60-64
,共5页
刘琴%陈芳%杨丽君%王丽平%朱以良%张宜
劉琴%陳芳%楊麗君%王麗平%硃以良%張宜
류금%진방%양려군%왕려평%주이량%장의
间充质干细胞%免疫表型%成脂诱导%成骨分化%低温冻存
間充質榦細胞%免疫錶型%成脂誘導%成骨分化%低溫凍存
간충질간세포%면역표형%성지유도%성골분화%저온동존
Mesenchymal stem cells%Immunophenotypes%Adipogenic induction%Osteogenic differentiation%Cryopreservation
目的:研究低温冻存对兔脂肪间充质干细胞部分生物学特性的影响。方法采用组织块法分离培养兔脂肪间充质干细胞。用倒置显微镜观察原代细胞的细胞形态,流式细胞仪检测兔脂肪间充质干细胞的免疫表型。取第3代兔脂肪间充质干细胞置于-196℃液氮保存半年,37℃复苏并传至第7代。实验分为两组,实验组为冻存复苏后传至第7代的兔脂肪间充质干细胞,对照组为未冻存的第7代兔脂肪间充质干细胞,用MTT绘制其生长曲线;添加成脂、成骨诱导液进行诱导,油红O、茜素红染色和碱性磷酸酶活性检测分别进行鉴定。结果体外培养的兔脂肪间充质干细胞呈梭形纤维样细胞形态,生长力旺盛。流式细胞仪检测显示,第3代兔脂肪间充质干细胞强表达CD44、CD90,阴性表达造血细胞相关的表面标志CD45。两组细胞生长曲线呈典型的“S”形,无统计学差异(P>0.05);成脂诱导14 d后,油红O染色呈阳性;成骨诱导2周时茜素红染色阳性,ALP表达活性随成骨诱导时间延长不断增加且无统计学差异( P>0.05)。结论冻存后的兔脂肪间充质干细胞体外生长及多向分化潜能未发生显著变化。
目的:研究低溫凍存對兔脂肪間充質榦細胞部分生物學特性的影響。方法採用組織塊法分離培養兔脂肪間充質榦細胞。用倒置顯微鏡觀察原代細胞的細胞形態,流式細胞儀檢測兔脂肪間充質榦細胞的免疫錶型。取第3代兔脂肪間充質榦細胞置于-196℃液氮保存半年,37℃複囌併傳至第7代。實驗分為兩組,實驗組為凍存複囌後傳至第7代的兔脂肪間充質榦細胞,對照組為未凍存的第7代兔脂肪間充質榦細胞,用MTT繪製其生長麯線;添加成脂、成骨誘導液進行誘導,油紅O、茜素紅染色和堿性燐痠酶活性檢測分彆進行鑒定。結果體外培養的兔脂肪間充質榦細胞呈梭形纖維樣細胞形態,生長力旺盛。流式細胞儀檢測顯示,第3代兔脂肪間充質榦細胞彊錶達CD44、CD90,陰性錶達造血細胞相關的錶麵標誌CD45。兩組細胞生長麯線呈典型的“S”形,無統計學差異(P>0.05);成脂誘導14 d後,油紅O染色呈暘性;成骨誘導2週時茜素紅染色暘性,ALP錶達活性隨成骨誘導時間延長不斷增加且無統計學差異( P>0.05)。結論凍存後的兔脂肪間充質榦細胞體外生長及多嚮分化潛能未髮生顯著變化。
목적:연구저온동존대토지방간충질간세포부분생물학특성적영향。방법채용조직괴법분리배양토지방간충질간세포。용도치현미경관찰원대세포적세포형태,류식세포의검측토지방간충질간세포적면역표형。취제3대토지방간충질간세포치우-196℃액담보존반년,37℃복소병전지제7대。실험분위량조,실험조위동존복소후전지제7대적토지방간충질간세포,대조조위미동존적제7대토지방간충질간세포,용MTT회제기생장곡선;첨가성지、성골유도액진행유도,유홍O、천소홍염색화감성린산매활성검측분별진행감정。결과체외배양적토지방간충질간세포정사형섬유양세포형태,생장력왕성。류식세포의검측현시,제3대토지방간충질간세포강표체CD44、CD90,음성표체조혈세포상관적표면표지CD45。량조세포생장곡선정전형적“S”형,무통계학차이(P>0.05);성지유도14 d후,유홍O염색정양성;성골유도2주시천소홍염색양성,ALP표체활성수성골유도시간연장불단증가차무통계학차이( P>0.05)。결론동존후적토지방간충질간세포체외생장급다향분화잠능미발생현저변화。
Objective To study the effect of cryopreservation on some biological properties of rabbit adipose -de-rived mesenchymal stem cells (rADMSCs).Methods rADMSCs culture was isolated by tissue explants adherent meth-od.Morphology of the primary cells was observed by inverted microscopy .Immunophenotypes of the rADMSCs were deter-mined using flow cytometry .The third passage cells were preserved in liquid nitrogen for 6 months, and then were thawed , and subcultured to passage 7.The growth curves of the cryopreserved cells were analyzed by MTT assay , and the cryopre-served cells were cultured in adipogenic and osteogenic medium , with non-cryopreserved rADMSCs as a control group .The adipogenic and osteogenic abilities of the rADMSCs were evaluated by oil red O staining , alizarin red staining and alkaline phosphatase activity assay , respectively.Results The rADMSCs cultured in vitro exhibited a spindle-shaped appearance and rapid growth expansion .Flow cytometry analysis revealed that the third passage rADMSCs were CD 44-and CD90-posi-tive, but negative for hematopoietic cells surface marker CD 45.The growth curves of cells in the experimental and control groups were “S” shaped, showing a non-significant difference between the two groups (P>0.05).The oil red O staining and alizarin red staining results were positive at 2 weeks after adipogenic and osteogenic induction .The ALP activities of the two groups were increased with osteogenic induction time , with a non-significant difference (P>0.05).Conclusions Cryopreservation does not affect the growth and differentiation pluripotency of rADMSCs significantly .