山东医药
山東醫藥
산동의약
SHANDONG MEDICAL JOURNAL
2014年
42期
17-19
,共3页
拾莉%张德明%任思坡%韩光宇%谭昆%耿跃春%梁军
拾莉%張德明%任思坡%韓光宇%譚昆%耿躍春%樑軍
습리%장덕명%임사파%한광우%담곤%경약춘%량군
糖尿病%脂肪间充质干细胞%分化潜能
糖尿病%脂肪間充質榦細胞%分化潛能
당뇨병%지방간충질간세포%분화잠능
diabetes mellitus%adipose tissue-derived stromal cells%differentiation potential
目的:探讨体外分离培养糖尿病患者脂肪间充质干细胞(ADSCs)的方法并分析其生物学特性。方法采用胶原酶消化法从糖尿病患者的脂肪组织中分离出ADSCs。对ADSCs进行体外培养,倒置相差显微镜下观察细胞形态;绘制第3、6、8代传代细胞的生长曲线;流式细胞仪检测第3代细胞表面标记物( CD34、CD45、CD29、CD44、CD105、CD90);通过成脂诱导实验鉴定细胞的分化潜能(油红染色阳性判定为脂肪细胞,证实细胞可向脂肪细胞分化)。结果分离出的ADSCs,能稳定传代;其细胞表面标记物CD34、CD45呈阴性表达,CD29、CD90、CD44、CD105呈阳性表达。成脂诱导后油红染色阳性。结论在糖尿病患者脂肪组织中成功分离到ADSCs,在体外适宜条件下ADSCs可向脂肪细胞分化,具有分化潜能。
目的:探討體外分離培養糖尿病患者脂肪間充質榦細胞(ADSCs)的方法併分析其生物學特性。方法採用膠原酶消化法從糖尿病患者的脂肪組織中分離齣ADSCs。對ADSCs進行體外培養,倒置相差顯微鏡下觀察細胞形態;繪製第3、6、8代傳代細胞的生長麯線;流式細胞儀檢測第3代細胞錶麵標記物( CD34、CD45、CD29、CD44、CD105、CD90);通過成脂誘導實驗鑒定細胞的分化潛能(油紅染色暘性判定為脂肪細胞,證實細胞可嚮脂肪細胞分化)。結果分離齣的ADSCs,能穩定傳代;其細胞錶麵標記物CD34、CD45呈陰性錶達,CD29、CD90、CD44、CD105呈暘性錶達。成脂誘導後油紅染色暘性。結論在糖尿病患者脂肪組織中成功分離到ADSCs,在體外適宜條件下ADSCs可嚮脂肪細胞分化,具有分化潛能。
목적:탐토체외분리배양당뇨병환자지방간충질간세포(ADSCs)적방법병분석기생물학특성。방법채용효원매소화법종당뇨병환자적지방조직중분리출ADSCs。대ADSCs진행체외배양,도치상차현미경하관찰세포형태;회제제3、6、8대전대세포적생장곡선;류식세포의검측제3대세포표면표기물( CD34、CD45、CD29、CD44、CD105、CD90);통과성지유도실험감정세포적분화잠능(유홍염색양성판정위지방세포,증실세포가향지방세포분화)。결과분리출적ADSCs,능은정전대;기세포표면표기물CD34、CD45정음성표체,CD29、CD90、CD44、CD105정양성표체。성지유도후유홍염색양성。결론재당뇨병환자지방조직중성공분리도ADSCs,재체외괄의조건하ADSCs가향지방세포분화,구유분화잠능。
Objective To establish the isolation and culture method of adipose mesenchymal stem cells derived from diabetic patients in vitro, so as to observe biological properties.Methods The ADSCs were isolated by digestion with col-lagenase from adipose tissue of diabetic patients, then cultured and purified in vitro.The cells were observed by inverted microscopeand.The P3, P6, P8 generation cells were collected and analyzed the cell growth curve.Then the cell surface markers and karyotype analysis of the P3 generation cells were detected.Their differentiation potential was proved by adipo-genic differentiation.Oil red staining positive proved they were fat cells.Results After isolation and culture, we obtained the ADSCs, which could passage stably and proliferate highly.The flow cytometry examination showed that the expression of CD34 and CD45 were negative, CD29 , CD90 , CD44 and CD105 were positive.Oil red staining was positive.Conclusion The ADSCs could be isolated from diabetic patients adipose tissue and be functionally induced into adipocytes in the pres-ence of appropriate conditioned media.