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人脂肪来源干细胞复合I型胶原支架构建工程化脂肪组织的实验研究
引用本文:张云松,高建华,鲁峰,朱茗,廖云君,李华. 人脂肪来源干细胞复合I型胶原支架构建工程化脂肪组织的实验研究[J]. 中华整形外科杂志, 2008, 24(5)
作者姓名:张云松  高建华  鲁峰  朱茗  廖云君  李华
作者单位:1. 广州市红十字会医院/暨南大学第四附属医院整形外科,510220
2. 南方医科大学附属南方医院整形外科,广州,510515
摘    要:目的 探讨构建组织工程化脂肪组织的可行性,为临床修复软组织缺损寻找一种新方法.方法 以酶消化法从人脂肪抽吸术抽吸物脂质部分获取人脂肪来源干细胞作为种子细胞,并行Dil体外荧光标记,以Ⅰ型胶原支架为载体材料,将细胞成脂诱导后,以1×107/ml细胞密度与支架复合后接种于裸鼠左侧背部皮下,未诱导组不对细胞进行任何诱导,以相同方式接种于裸鼠右侧背部皮下,空白对照组将Ⅰ型胶原空白支架接种于裸鼠颈部正中皮下,每组各6只实验鼠;于第12周取材,通过大体和荧光显微镜观察、湿重测定、组织学检测和油红0染色定性判断体内成脂能力.结果 原代培养的脂肪来源干细胞,经成脂诱导能演变为成熟脂肪细胞,油红0染色阳性.诱导组裸鼠皮下均发现新生组织块,新生物平均湿重为0.020 g,常规病理切片及油红0染色均证实其为成熟脂肪组织,Dil荧光显色阳性证实其为外源性;未诱导组4只裸鼠皮下发现新生组织块,新生物平均湿重为0.014 g,常规病理切片及油红0染色证实其含有部分成熟脂肪组织,Dil荧光显色阳性证实其为外源性.两组新生物湿重比较差异有统计学意义(P<0.01);空白对照组未见新生组织形成.结论 用酶消化法从人脂肪抽吸术抽吸物脂质部分提取的细胞为脂肪组织来源干细胞,该细胞能作为种子细胞经成脂诱导后.与Ⅰ型胶原支架在体内成功构建脂肪组织.

关 键 词:脂肪组织  干细胞  组织工程  胶原Ⅰ型  支架

Study of adipose tissue engineering with human adipose-derived stem cells and collagen type I scaffold
ZHANG Yun-song,GAO Jian-hua,LU Feng,ZHU Ming,LIAO Yun-jun,LI Hua. Study of adipose tissue engineering with human adipose-derived stem cells and collagen type I scaffold[J]. Chinese journal of plastic surgery, 2008, 24(5)
Authors:ZHANG Yun-song  GAO Jian-hua  LU Feng  ZHU Ming  LIAO Yun-jun  LI Hua
Abstract:Objective To explore the possibility of building tissue-engineered adipose tissue and looking for a new approach for the repair of soft tissue defects.Methods The ceils using enzymatic digestion from human liposuction part of the lipid extract were used as adipose tissue-derived cells and labeled with Dil fluorescent marker.theinduced group using I collagen scaffold material as a carrier.the induced cell were planted into left back subcutaneously in nude mice at 1×107/ml cell density.in the uninduced group cells were not induced by any.in the game cell density and type Ⅰ collagen scaffold composite inoculated in nude right mouse back skin,the blank control group Ⅰ collagen scaffold gaps in nude mice inoculated subcutaneously center of the neck,eachof the six mice;Remove implants after 12 weeks and judge the adipogenic capacity through general and fluorescence microscopy,wet-determination,histological detection and oil red O staining qualitative.Results The primmT source of fat cultured stem cells,similar to the fibroblast morphology,and has a strong proliferative capacity.In the role of adipose differentiation medium,it can be the mature fat cells in which cytoplasmic lipid droplets gather,oil red O staaining wsa positive.In the induced group,newborn tissue were found in the experimental groups of nude mice and its average weight is about 0.020 g.Conventional pathological glices and oil red O staining confirmed it is mature adipose tissue.the fluorescence smining positive cerium them are exogenous.Unindnced group newborn tissue are found in the experimental groups of nude mice and its average weight is about 0.014 g.Conventional pathological slices and oil red O staining confirmed it include some mature adipose tissue,the fluorescence staining positive confirm them are exogenous.Two groups of the new wet weight with have statistical significance (P<0.01);gaps in the control group no new organization formed.Conclusions The cells using enzymatic digestion from human lipesuction part of the lipid extract are adipose tissue-derived cells.The cells can be as seed cells and with solid scaffold of collagen type I it can become fat tissue in vivo successfully.
Keywords:Adipose tissue  Stem cells  Tissue engineering  Collagen type Ⅰ  Stents
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