Phenotypic and functional properties of feline dedifferentiated fat cells and adipose-derived stem cells

被引:47
|
作者
Kono, Shota [1 ]
Kazama, Tomohiko [2 ]
Kano, Koichiro [3 ]
Harada, Kayoko [1 ]
Uechi, Masami [1 ]
Matsumoto, Taro [2 ]
机构
[1] Nihon Univ, Lab Vet Internal Med, Dept Vet Med, Coll Bioresource Sci, Fujisawa, Kanagawa 2520880, Japan
[2] Nihon Univ, Sch Med, Dept Funct Morphol, Div Cell Regenerat & Transplantat, Tokyo 1738610, Japan
[3] Nihon Univ, Lab Cell & Tissue Biol, Coll Bioresource Sci, Fujisawa, Kanagawa 2520880, Japan
基金
日本科学技术振兴机构;
关键词
Adipose-derived stem cell; Feline; Mature adipocyte; Mesenchymal stem cell; Regenerative medicine; MESENCHYMAL STROMAL CELLS; BONE-MARROW; IN-VITRO; TEMPORAL-CHANGES; TISSUE; DIFFERENTIATION; TRANSPLANTATION; DYSFUNCTION; MEDICINE; DFAT;
D O I
10.1016/j.tvjl.2013.10.033
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
It has been reported that mature adipocyte-derived dedifferentiated fat (DFAT) cells show multilineage differentiation potential similar to that observed in mesenchymal stem cells. Since DFAT cells can be prepared from a small quantity of adipose tissue, they could facilitate cell-based therapies in small companion animals such as cats. The present study examined whether multipotent DFAT cells can be generated from feline adipose tissue, and the properties of DFAT cells were compared with those of adipose-derived stem cells (ASCs). DFAT cells and ASCs were prepared from the floating mature adipocyte fraction and the stromal vascular fraction, respectively, of collagenase-digested feline omental adipose tissue. Both cell types were evaluated for growth kinetics, colony-forming unit fibroblast (CFU-F) frequency, immunophenotypic properties, and multilineage differentiation potential. DFAT cells and ASCs could be generated from approximately 1 g of adipose tissue and were grown and subcultured on laminin-coated dishes. The frequency of CFU-Fs in DFAT cells (35.8%) was significantly higher than that in ASCs (20.8%) at passage 1 (P1). DFAT cells and ASCs displayed similar immunophenotypes (CD44(+), CD90(+), CD105(+), CD14(-), CD34(-) and CD45(-)). Alpha-smooth muscle actin-positive cells were readily detected in ASCs (15.2 +/- 7.2%) but were rare in DFAT cells (2.2 +/- 3.2%) at P1. Both cell types exhibited adipogenic, osteogenic, chondrogenic, and smooth muscle cell differentiation potential in vitro. In conclusion, feline DFAT cells exhibited similar properties to ASCs but displayed higher CPU-F frequency and greater homogeneity. DFAT cells, like ASCs, may be an attractive source for cell-based therapies in cats. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:88 / 96
页数:9
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