The Effect of Storage Time on Adipose-Derived Stem Cell Recovery from Human Lipoaspirates

被引:41
|
作者
Carvalho, Pedro P. [1 ,2 ,3 ]
Wu, Xiying [1 ]
Yu, Gang [1 ]
Dias, Isabel R. [2 ,3 ,4 ]
Gomes, Manuela E. [2 ,3 ]
Reis, Rui L. [2 ,3 ]
Gimble, Jeffrey M. [1 ]
机构
[1] Louisiana State Univ Syst, Stem Cell Biol Lab, Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA
[2] Univ Minho, Res Grp Biomat Biodegradables & Biomimet 3Bs, Headquarters European Inst Excellence Tissue Engn, Guimaraes, Portugal
[3] PT Associated Lab, Inst Bioengn & Biotechnol, IBB, Braga, Portugal
[4] Univ Tras Os Montes & Alto Douro, Sch Agr & Vet Sci, Dept Vet Sci, Vila Real, Portugal
关键词
Adipose-derived stem cells; Cell yield; Differentiation; Lipoaspirate; Tissue storage; COMPLEX PERIANAL FISTULA; ASSISTED LIPOTRANSFER; SUPPORTIVE USE; STROMAL CELLS; TISSUE; DIFFERENTIATION; TRANSPLANTATION; AUGMENTATION; YIELD;
D O I
10.1159/000324892
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Multipotent adipose-derived stromal/stem cells (ASCs) can be isolated with high yield from human subcutaneous lipoaspirates. This study reports our experience isolating, expanding, differentiating and immunophenotypically characterizing ASCs over a period of 4 days after having surgically obtained the lipoaspirate samples. The ultimate goal is to understand how to optimize the consistent isolation of ASCs from lipoaspirates. The length of time between adipose tissue harvest and processing will need to be systematically evaluated with respect to cell yield, viability, and function since some distance is likely to exist between the plastic surgeon's office where lipoaspiration is performed and the current Good Manufacturing Practices (cGMP) laboratory where the ASCs are isolated. The objective of this study was to determine the effect of time delays on the yield and function of ASCs after collagenase digestion. We were able to isolate ASCs from lipoaspirates up to 72 h after the surgical procedure. The ASCs isolated on sequential days after the original tissue harvest proliferated, differentiated and maintained cell surface markers. We found that the initial 24-hour period is optimal for isolating ASCs with respect to cell yield and that there was no significant difference between ASC cell proliferation and differentiation ability within this period of time. In contrast, each of these parameters declined significantly for tissues maintained at room temperature for 48 or 72 h prior to isolation. These findings should be considered in the future development of standard operating procedures for cGMP processing of clinical-grade human ASCs. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:494 / 500
页数:7
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