Genetic modification of ex-vivo expanded stem cells for clinical application

被引:9
作者
Aggarwal, Reeva [1 ]
Pompili, Vincent J. [1 ]
Das, Hiranmoy [1 ]
机构
[1] Ohio State Univ, Med Ctr, Cardiovasc Stem Cell Res Lab, Dorothy M Davis Heart & Lung Res Inst, Columbus, OH 43210 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2010年 / 15卷
基金
美国国家卫生研究院;
关键词
Hematopoietic Stem Cells; Niche; Genetic Modification; Virus; Transduction; Non-Viral; Ex-Vivo; Expansion; Ischemia; Pro-Angiogenic Factors; Neo-vascularization; Review; ENDOTHELIAL GROWTH-FACTOR; CORD BLOOD TRANSPLANTATION; HUMAN HEMATOPOIETIC-CELLS; COLONY-STIMULATING FACTOR; IN-VITRO; PROGENITOR CELLS; EFFICIENT TRANSFECTION; THERAPEUTIC ANGIOGENESIS; REPOPULATING CELLS; SELF-RENEWAL;
D O I
10.2741/3650
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Stem cell therapy is currently considered as an important regime for repairing, replacing or enhancing the biological functions of the damaged tissues. Among adult stem cells, hematopoietic stem cells (HSCs) are commonly used for cure of hematological disorders. However, the number of HSCs obtained from sources like bone marrow, peripheral or umbilical cord blood is not sufficient for routine clinical application. Thus, ex-vivo expansion of HSCs becomes critically important. Ex-vivo culture and expansion of stem cells are challenging, as stem cells differentiate in culture rather than self-renew. Lack of clarity about the factors responsible for quiescence and differentiation of HSCs, investigators struggled to optimize conditions for ex vivo expansion. As we understand better, various strategies can be incorporated to mimic in vivo conditions for successful expansion of stem cells. However, characterization and biological functionality should also be tested for expanded stem cells prior to clinical application. To treat ischemia by enhancing therapeutic angiogenesis and neo-vascularization, the role of genetic modification of HSCs with pro-angiogenic factors is the focus of this review.
引用
收藏
页码:854 / 871
页数:18
相关论文
共 165 条
[1]   The hematopoietic stem cell in its place [J].
Adams, GB ;
Scadden, DT .
NATURE IMMUNOLOGY, 2006, 7 (04) :333-337
[2]   Nucleofection is an efficient nonviral transfection technique for human bone marrow-derived mesenchymal stem cells [J].
Aluigi, Michela ;
Fogli, Miriam ;
Curti, Antonio ;
Isidori, Alessandro ;
Gruppioni, Elisa ;
Chiodoni, Claudia ;
Colombo, Mario P. ;
Versura, Piera ;
D'Errico-Grigioni, Antonia ;
Ferri, Elisa ;
Baccarani, Michele ;
Lemoli, Roberto M. .
STEM CELLS, 2006, 24 (02) :454-461
[3]   A theoretical simulation of hematopoietic stem cells during oxygen fluctuations: Prediction of bone marrow responses during hemorrhagic shock [J].
Antoniou, ES ;
Sund, S ;
Homsi, EN ;
Challenger, LF ;
Rameshwar, P .
SHOCK, 2004, 22 (05) :415-422
[4]  
APPERLEY JF, 1994, BONE MARROW TRANSPL, V14, P187
[5]   Tie2/angiopoietin-1 signaling regulates hematopoietic stem cell quiescence in the bone marrow niche [J].
Arai, F ;
Hirao, A ;
Ohmura, M ;
Sato, H ;
Matsuoka, S ;
Takubo, K ;
Ito, K ;
Koh, GY ;
Suda, T .
CELL, 2004, 118 (02) :149-161
[6]   Monocyte activation in angiogenesis and collateral growth in the rabbit hindlimb [J].
Arras, M ;
Ito, WD ;
Scholz, D ;
Winkler, B ;
Schaper, J ;
Schaper, W .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (01) :40-50
[7]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[8]   VEGF contributes to postnatal neovascularization by mobilizing bone marrow-derived endothelial progenitor cells [J].
Asahara, T ;
Takahashi, T ;
Masuda, H ;
Kalka, C ;
Chen, DH ;
Iwaguro, H ;
Inai, Y ;
Silver, M ;
Isner, JM .
EMBO JOURNAL, 1999, 18 (14) :3964-3972
[9]   Role of PIGF in the intra- and intermolecular cross talk between the VEGF receptors Flt1 and Flk1 [J].
Autiero, M ;
Waltenberger, J ;
Communi, D ;
Kranz, A ;
Moons, L ;
Lambrechts, D ;
Kroll, J ;
Plaisance, S ;
De Mol, M ;
Bono, F ;
Kliche, S ;
Fellbrich, G ;
Ballmer-Hofer, K ;
Maglione, D ;
Mayr-Beyrle, U ;
Dewerchin, M ;
Dombrowski, S ;
Stanimirovic, D ;
Van Hummelen, P ;
Dehio, C ;
Hicklin, DJ ;
Persico, G ;
Herbert, JM ;
Communi, D ;
Shibuya, M ;
Collen, D ;
Conway, EM ;
Carmeliet, P .
NATURE MEDICINE, 2003, 9 (07) :936-943
[10]   Hypoxia-induced apoptosis in human hepatocellular carcinoma cells: a possible involvement of the 6-TG-sensitive protein kinase(s) dependent signaling pathway [J].
Bae, SK ;
Baek, JH ;
Lee, YM ;
Lee, OH ;
Kim, KW .
CANCER LETTERS, 1998, 126 (01) :97-104