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
[11]   VEGFR-1 (FLT-1) activation modulates acute lymphoblastic leukemia localization and survival within the bone marrow, determining the onset of extramedullary disease [J].
Fragoso, R ;
Pereira, T ;
Wu, Y ;
Zhu, ZP ;
Cabeçadas, J ;
Dias, S .
BLOOD, 2006, 107 (04) :1608-1616
[12]  
Horisberger MA, 2006, IN VITRO CELL DEV-AN, V42, P143
[13]   Engineering CD19-specific T lymphocytes with interleukin-15 and a suicide gene to enhance their anti-lymphoma/leukemia effects and safety [J].
Hoyos, V. ;
Savoldo, B. ;
Quintarelli, C. ;
Mahendravada, A. ;
Zhang, M. ;
Vera, J. ;
Heslop, H. E. ;
Rooney, C. M. ;
Brenner, M. K. ;
Dotti, G. .
LEUKEMIA, 2010, 24 (06) :1160-1170
[14]   In vitro validation of bioluminescent monitoring of disease progression and therapeutic response in leukaemia model animals [J].
Inoue, Y ;
Tojo, A ;
Sekine, R ;
Soda, Y ;
Kobayashi, S ;
Nomura, A ;
Izawa, K ;
Kitamura, T ;
Okubo, T ;
Ohtomo, K .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2006, 33 (05) :557-565
[15]   Monitoring of disease progression by bioluminescence imaging and magnetic resonance imaging in an animal model of hematologic malignancy [J].
Inoue, Yusuke ;
Izawa, Kiyoko ;
Tojo, Arinobu ;
Nomura, Yukihiro ;
Sekine, Rieko ;
Oyaizu, Naoki ;
Ohtomo, Kuni .
EXPERIMENTAL HEMATOLOGY, 2007, 35 (03) :407-415
[16]   Bioluminescent evaluation of the therapeutic effects of total body irradiation in a murine hematological malignancy model [J].
Inoue, Yusuke ;
Izawa, Kiyoko ;
Kiryu, Shigeru ;
Kobayashi, Seiichiro ;
Tojo, Arinobu ;
Ohtomo, Kuni .
EXPERIMENTAL HEMATOLOGY, 2008, 36 (12) :1634-1641
[17]   Bioluminescent imaging (BLI) to improve and refine traditional murine models of tumor growth and metastasis [J].
Jenkins, DE ;
Oei, Y ;
Hornig, YS ;
Yu, SF ;
Dusich, J ;
Purchio, T ;
Contag, PR .
CLINICAL & EXPERIMENTAL METASTASIS, 2003, 20 (08) :733-744
[18]   AID-induced T-lymphoma or B-leukemia/lymphoma in a mouse BMT model [J].
Komeno, Y. ;
Kitaura, J. ;
Watanabe-Okochi, N. ;
Kato, N. ;
Oki, T. ;
Nakahara, F. ;
Harada, Y. ;
Harada, H. ;
Shinkura, R. ;
Nagaoka, H. ;
Hayashi, Y. ;
Honjo, T. ;
Kitamura, T. .
LEUKEMIA, 2010, 24 (05) :1018-1024
[19]   Stromal cells prevent apoptosis of AML cells by up-regulation of anti-apoptotic proteins [J].
Konopleva, M ;
Konoplev, S ;
Hu, W ;
Zaritskey, AY ;
Afanasiev, BV ;
Andreeff, M .
LEUKEMIA, 2002, 16 (09) :1713-1724
[20]   "Microenvironmental contaminations" induced by fluorescent lipophilic dyes used for noninvasive in vitro and in vivo cell tracking [J].
Lassailly, Francois ;
Griessinger, Emmanuel ;
Bonnet, Dominique .
BLOOD, 2010, 115 (26) :5347-5354