Establishment of a bioluminescent imaging-based in vivo leukemia model by intra-bone marrow injection

被引:10
作者
Lee, Myoung Woo [1 ]
Kim, Hye Jin [1 ]
Yoo, Keon Hee [1 ]
Kim, Dae Seong [1 ]
Yang, Jin Mo [1 ]
Kim, Hye Ryung [1 ]
Noh, Yoo Hun [1 ]
Baek, Hyunjung [2 ]
Kwon, Heechung [2 ]
Son, Meong Hi [1 ]
Lee, Soo Hyun [1 ]
Cheuh, Hee Won [3 ]
Jung, Hye Lim [1 ]
Sung, Ki Woong [1 ]
Koo, Hong Hoe [1 ]
机构
[1] Sungkyunkwan Univ, Dept Pediat, Samsung Med Ctr, Sch Med, Seoul 135710, South Korea
[2] Korea Inst Radiol & Med Sci, Div Radiat Oncol, Seoul, South Korea
[3] Dong A Univ, Dept Pediat, Dong A Med Ctr, Coll Med, Pusan, South Korea
基金
新加坡国家研究基金会;
关键词
leukemia; intra-bone marrow transplantation; firefly luciferase; bioluminescent imaging; animal model; ACUTE LYMPHOBLASTIC-LEUKEMIA; DISEASE PROGRESSION; GENE-EXPRESSION; XENOGRAFT MODEL; T-LYMPHOCYTES; NOD/SCID MICE; UP-REGULATION; ANIMAL-MODEL; MOUSE MODEL; CELL;
D O I
10.3892/ijo.2012.1634
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In vivo leukemia mouse models are usually generated by intraperitoneal (IP) or intravenous (IV) injection of leukemia cells. However, the pattern of leukemia development observed can be inconsistent. This study investigated injection directly into bone marrow [intra-bone marrow transplantation (IBMT)], the natural microenvironment of leukemia. A bioluminescent imaging-based leukemia animal model has been established by direct injection of a bioluminescent leukemia cells (CCRF-CEM/fLuc) into NOD/SCID mouse tibia bone marrow and compared with models established by IP and IV routes. The comparison revealed that a bioluminescent in vivo leukemia model established via IBMT could recapitulate leukemia more faithfully and facilitate improved quantification of leukemia engraftment kinetics with a wider range of bioluminescent intensity than IP or IV. IBMT of bioluminescent leukemic cells allowed quantification of dose-dependent responses to anti-leukemic drugs, thus validating this model as a potential preclinical anti-leukemic drug screening system. IBMT-leukemia cells isolated from peripheral blood of the model mice and then injected into new recipients successfully established a second generation IBMT in vivo model and demonstrated the reproducibility of the model. Bioluminescent imaging-based analysis of this IBMT-leukemia model could provide a means for the comprehensive evaluation of treatment responses with enhanced sensitivity in preclinical studies.
引用
收藏
页码:2047 / 2056
页数:10
相关论文
共 39 条
[1]   Contribution of bone microenvironment to leukemogenesis and leukemia progression [J].
Ayala, F. ;
Dewar, R. ;
Kieran, M. ;
Kalluri, R. .
LEUKEMIA, 2009, 23 (12) :2233-2241
[2]   Modeling the initiation and progression of human acute leukemia in mice [J].
Barabe, Frederic ;
Kennedy, James A. ;
Hope, Kristin J. ;
Dick, John E. .
SCIENCE, 2007, 316 (5824) :600-604
[3]   Noninvasive bioluminescent imaging of primary patient acute lymphoblastic leukemia: a strategy for preclinical modeling [J].
Barrett, David M. ;
Seif, Alix E. ;
Carpenito, Carmine ;
Teachey, David T. ;
Fish, Jonathan D. ;
June, Carl H. ;
Grupp, Stephan A. ;
Reid, Gregor S. D. .
BLOOD, 2011, 118 (15) :E112-E117
[4]   Evaluation of the NOD/SCID xenograft model for glucocorticoid-regulated gene expression in childhood B-cell precursor acute lymphoblastic leukemia [J].
Bhadri, Vivek A. ;
Cowley, Mark J. ;
Kaplan, Warren ;
Trahair, Toby N. ;
Lock, Richard B. .
BMC GENOMICS, 2011, 12
[5]  
Biagi E, 2001, HAEMATOLOGICA, V86, P13
[6]   Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell [J].
Bonnet, D ;
Dick, JE .
NATURE MEDICINE, 1997, 3 (07) :730-737
[7]  
CESANO A, 1991, BLOOD, V77, P2463
[8]   Leukemic Cells Create Bone Marrow Niches That Disrupt the Behavior of Normal Hematopoietic Progenitor Cells [J].
Colmone, Angela ;
Amorim, Maria ;
Pontier, Andrea L. ;
Wang, Sheng ;
Jablonski, Elizabeth ;
Sipkins, Dorothy A. .
SCIENCE, 2008, 322 (5909) :1861-1865
[9]   Beyond RECIST: Molecular and functional imaging techniques for evaluation of response to targeted therapy [J].
Desar, I. M. E. ;
van Herpen, C. M. L. ;
van Laarhoven, H. W. M. ;
Barentsz, J. O. ;
Oyen, W. J. G. ;
van der Graaf, W. T. A. .
CANCER TREATMENT REVIEWS, 2009, 35 (04) :309-321
[10]   Antileukaemic activity of treosulfan in xenografted human acute lymphoblastic leukaemias (ALL) [J].
Fichtner, I ;
Becker, M ;
Baumgart, J .
EUROPEAN JOURNAL OF CANCER, 2003, 39 (06) :801-807