Expansion of engrafting human hematopoietic stem/progenitor cells in three-dimensional scaffolds with surface-immobilized fibronectin

被引:105
作者
Feng, Qi
Chai, Chou
Jiang, Xue-Song
Leong, Kam W.
Mao, Hai-Quan
机构
[1] Div Biomed Sci, Singapore 138669, Singapore
[2] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Dept Mat Sci & Engn, Baltimore, MD 21218 USA
[4] Johns Hopkins Univ, Whitaker Biomed Engn Inst, Baltimore, MD 21218 USA
关键词
hematopoietic stem cells; expansion; scaffold; fibronectin; immobilization;
D O I
10.1002/jbm.a.30829
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
An efficient and practical ex vivo expansion methodology for human hematopoietic stem/progenitor cells (HSPCs) is critical in realizing the potential of HSPC transplantation in treating a variety of hematologic disorders and as a supportive therapy for malignant diseases. We report here an expansion strategy using a three-dimensional (3D) scaffold conjugated with an extracellular matrix molecule, fibronectin (FN), to partially mimic the hematopoietic stem cell niche. FN-immobilized 3D polyethylene terephthalate (PET) scaffold was synthesized and evaluated for HSPC expansion efficiency, in comparison with a FN-immobilized 2D PET substrate and a 3D scaffold with FN supplemented in the medium. Covalent conjugation of IN produced substrate and scaffold with higher cell expansion efficiency than that on their unmodified counterparts. After 10 days of culture in serum-free medium, human umbilical cord blood CD34(+) cells cultured in FN-conjugated scaffold yielded the highest expansion of CD34(+) cells (similar to 100 fold) and long-term culture initiating cells (similar to 47-fold). The expanded human CD34(+) cells successfully reconstituted hematopoiesis in NOD/SCID mice. This study demonstrated the synergistic effect between the three-dimensionality of the scaffold and surface-conjugated FN, and the potential of this FN-conjugated 3D scaffold for ex vivo expansion of HSPCs. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:781 / 791
页数:11
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