Phenotypic and functional characterization of human bone marrow stromal cells in hollow-fibre bioreactors

被引:9
|
作者
Li, Matthew [1 ]
Tilles, Arno W. [3 ]
Milwid, Jack M. [1 ,2 ]
Hammad, Mohamed [1 ]
Lee, Jungwoo [1 ]
Yarmush, Martin L. [1 ]
Parekkadan, Biju [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Engn Med & Surg Serv,Shriners Hosp Children, Boston, MA USA
[2] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[3] Sentien Biotechnol Inc, Medford, MA USA
基金
美国国家卫生研究院;
关键词
mesenchymal stem cell; dialysis; acute kidney failure; MESENCHYMAL STEM-CELLS; VERSUS-HOST-DISEASE; MYOCARDIAL-INFARCTION; RENAL-FAILURE; IN-VITRO; ACTIVATION; MICE; LUNG; VIVO; INTERLEUKIN-6-DEFICIENT;
D O I
10.1002/term.439
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The transplantation of human bone marrow stromal cells (BMSCs) is a novel immunotherapeutic approach that is currently being explored in many clinical settings. Evidence suggests that the efficacy of cell transplantation is directly associated with soluble factors released by human BMSCs. In order to harness these secreted factors, we integrated BMSCs into large-scale hollow-fibre bioreactor devices in which the cells, separated by a semipermeable polyethersulphone (PES) membrane, can directly and continuously release therapeutic factors into the blood stream. BMSCs were found to be rapidly adherent and exhibited long-term viability on PES fibres. The cells also preserved their immunophenotype under physiological fluid flow rates in the bioreactor, and exhibited no signs of differentiation during device operation, but still retained the capacity to differentiate into osteoblastic lineages. BMSC devices released growth factors and cytokines at comparable levels on a per-cell basis to conventional cell culture platforms. Finally, we utilized a potency assay to demonstrate the therapeutic potential of the collected secreted factors from the BMSC devices. In summary, we have shown that culturing BMSCs in a large-scale hollow-fibre bioreactor is feasible without deleterious effects on phenotype, thus providing a platform for collecting and delivering the paracrine secretions of these cells. Copyright (C) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:369 / 377
页数:9
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