Automated collective motion analysis validates human keratinocyte stem cell cultures

被引:5
|
作者
Kinoshita, Koji [1 ]
Munesue, Takuya [1 ]
Toki, Fujio [2 ]
Isshiki, Masaharu [1 ]
Higashiyama, Shigeki [3 ,4 ]
Barrandon, Yann [5 ,6 ]
Nishimura, Emi K. [2 ]
Yanagihara, Yoshio [1 ]
Nanba, Daisuke [2 ]
机构
[1] Ehime Univ, Grad Sch Sci & Engn, 3 Bunkyo Cho, Matsuyama, Ehime 7908577, Japan
[2] Tokyo Med & Dent Univ, Med Res Inst, Dept Stem Cell Biol, Bunkyo Ku, 1-5-45 Yushima, Tokyo 1138510, Japan
[3] Ehime Univ, Div Cell Growth & Tumor Regulat, Proteosci Ctr, Toon, Ehime 7910295, Japan
[4] Ehime Univ, Grad Sch Med, Dept Biochem & Mol Genet, Shitsukawa, Ehime 7910295, Japan
[5] ASTAR, Inst Med Biol, Duke NUS Grad Med Sch, Singapore, Singapore
[6] Singapore Gen Hosp, Dept Plast Reconstruct & Aesthet Surg, Singapore, Singapore
关键词
EPITHELIAL-CELLS; TRANSPLANTATION; THERAPY; LOCATION;
D O I
10.1038/s41598-019-55279-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Identification and quality assurance of stem cells cultured in heterogeneous cell populations are indispensable for successful stem cell therapy. Here we present an image-processing pipeline for automated identification and quality assessment of human keratinocyte stem cells. When cultivated under appropriate conditions, human epidermal keratinocyte stem cells give rise to colonies and exhibit higher locomotive capacity as well as significant proliferative potential. Image processing and kernel density estimation were used to automatically extract the area of keratinocyte colonies from phase-contrast images of cultures containing feeder cells. The DeepFlow algorithm was then used to calculate locomotion speed of the colony area by analyzing serial images. This image-processing pipeline successfully identified keratinocyte stem cell colonies by measuring cell locomotion speed, and also assessed the effect of oligotrophic culture conditions and chemical inhibitors on keratinocyte behavior. Therefore, this study provides automated procedures for image-based quality control of stem cell cultures and high-throughput screening of small molecules targeting stem cells.
引用
收藏
页数:12
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