Fibronectin and laminin enhance engraftibility of cultured hematopoietic stem cells

被引:49
作者
Sagar, Balla Murali Mohan [1 ]
Rentala, Satyanarayana [1 ]
Gopal, P. N. V. [1 ]
Sharma, Shalini [1 ]
Mukhopadhyay, Asok [1 ]
机构
[1] Natl Inst Immunol, Stem Cell Biol Lab, New Delhi 110067, India
关键词
hematopoietic stem cells; extracellular matrix; cell adhesion molecules; primitiveness; veraparnil sensitivity; multi-lineage engraftibility;
D O I
10.1016/j.bbrc.2006.09.140
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
To test the hypothesis that extracellular matrix (ECM) components maintain stem cell property, murine bone marrow (BM) cells were expanded in fibronectin and laminin coated plate in the presence of cytokines. We observed significant phenotypic and functional improvement of expanded cells. In 10 days, 800-fold expansion of colony-forming unit-granulocyte erythrocyte monocyte megakaryocyte (CFU-GEMM) was observed in the cultured cells. No apparent activation of cell cycle was observed, but CD29 and very late antigen-4 (VLA-4) expression was increased, as compared to the normal BM cells. A fraction of the expanded cells became verapamil sensitive, suggesting upregulation of multi-drug resistant gene(s), as found in the primitive hematopoietic stem cells (HSCs). Competitive repopulation assay confirmed that HSCs compartment was amplified during culture. Overall, our study clearly demonstrated that ex vivo culture of murine HSCs in the presence of fibronectin and laminin resulted in expansion of primitive stem cells and improvement in the marrow engraftibility. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1000 / 1005
页数:6
相关论文
共 27 条
[1]
BAILLY JD, 1995, MOL PHARM, V47, P51
[2]
The molecular basis for the cytokine-induced defect in homing and engraftment of hematopoietic stem cells [J].
Berrios, VM ;
Dooner, GJ ;
Nowakowski, G ;
Frimberger, A ;
Valinski, H ;
Quesenberry, PJ ;
Becker, PS .
EXPERIMENTAL HEMATOLOGY, 2001, 29 (11) :1326-1335
[3]
Enforced P-glycoprotein pump function in murine bone marrow cells results in expansion of side population stem cells in vitro and repopulating cells in vivo [J].
Bunting, KD ;
Zhou, S ;
Lu, TH ;
Sorrentino, BP .
BLOOD, 2000, 96 (03) :902-909
[4]
Ex vivo culture rescues hematopoietic stem cells with long-term repopulating capacity following harvest from lethally irradiated mice [J].
Chute, JP ;
Fung, J ;
Muramoto, G ;
Erwin, R .
EXPERIMENTAL HEMATOLOGY, 2004, 32 (03) :308-317
[5]
Pluripotent hemopoietic stem cells are c-kit(<low) [J].
Doi, H ;
Inaba, M ;
Yamamoto, Y ;
Taketani, S ;
Mori, SI ;
Sugihara, A ;
Ogata, H ;
Toki, J ;
Hisha, H ;
Inaba, K ;
Sogo, S ;
Adachi, M ;
Matsuda, T ;
Good, RA ;
Ikehara, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2513-2517
[6]
Ex vivo expansion of stem cells from umbilical cord blood: Expression of cell adhesion molecules [J].
Dravid, G ;
Rao, SGA .
STEM CELLS, 2002, 20 (02) :183-189
[7]
Ex vivo expansion of human adult stem cells capable of primary and secondary hemopoietic reconstitution [J].
Gammaitoni, L ;
Bruno, S ;
Sanavio, F ;
Gunetti, M ;
Kollet, O ;
Cavalloni, G ;
Falda, M ;
Fagioli, F ;
Lapidot, T ;
Aglietta, M ;
Piacibello, W .
EXPERIMENTAL HEMATOLOGY, 2003, 31 (03) :261-270
[8]
ENDOSTEAL MARROW - RICH SOURCE OF HEMATOPOIETIC STEM-CELLS [J].
GONG, JK .
SCIENCE, 1978, 199 (4336) :1443-1445
[9]
Dye efflux studies suggest that hematopoietic stem cells expressing low or undetectable levels of CD34 antigen exist in multiple species [J].
Goodell, MA ;
Rosenzweig, M ;
Kim, H ;
Marks, DF ;
DeMaria, M ;
Paradis, G ;
Grupp, SA ;
Sieff, CA ;
Mulligan, RC ;
Johnson, RP .
NATURE MEDICINE, 1997, 3 (12) :1337-1345
[10]
Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo [J].
Goodell, MA ;
Brose, K ;
Paradis, G ;
Conner, AS ;
Mulligan, RC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (04) :1797-1806