NOD/SCID/γcnull mouse:: an excellent recipient mouse model for engraftment of human cells

被引:1116
|
作者
Ito, M
Hiramatsu, H
Kobayashi, K
Suzue, K
Kawahata, M
Hioki, K
Ueyama, Y
Koyanagi, Y
Sugamura, K
Tsuji, K
Heike, T
Nakahata, T
机构
[1] Kyoto Univ, Dept Pediat, Cent Inst Expt Anim, Grad Sch Med, Kawasaki, Kanagawa 2160001, Japan
[2] Gunma Univ, Dept Parasitol, Sch Med, Gunma, Japan
[3] Tokai Univ, Dept Pathol, Sch Med, Tokai, Ibaraki, Japan
[4] Tohoku Univ, Grad Sch Med, Dept Virol, Sendai, Miyagi 980, Japan
[5] Tohoku Univ, Grad Sch Med, Dept Immunol, Sendai, Miyagi 980, Japan
[6] Univ Tokyo, Div Cellular therapy, Adv Clin Res Ctr, Inst Med Sci, Tokyo, Japan
关键词
D O I
10.1182/blood-2001-12-0207
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To establish a more appropriate animal recipient for xenotransplantation, NOD SCID/gamma(c)(null) mice double homozygous for the severe combined immunodeficiency (SCID) mutation and interieukin-2Rgamma (IL-2Rgamma) allelic mutation (gamma(c)(null)) were generated by 8 backcross matings of C57BL/6J-gamma(c)(null) mice and NOD/Shi-scid mice. When human CD34(+) cells from umbilical cord blood were transplanted into this strain, the engraftment rate in the peripheral circulation, spleen, and bone marrow were significantly higher than that in NOD/Shi-scid mice treated with anti-asialo GM1 antibody or in the beta2-microglobulindeficient NOD/LtSz-scid (NOD/SCID/beta2m(null)) mice, which were as completely defective in NK cell activity as NOD/SCID/gamma(c)(null) mice. The same high engraftment rate of human mature cells was observed in ascites when peripheral blood mononuclear cells were intraperitoneally transferred. In addition to the high engraftment rate, multilineage cell differentiation was also observed. Further, even 1 x 10(2) CD34(+) cells could grow and differentiate in this strain. These results suggest that NOD/SCIO/gamma(c)(null) mice were superior animal recipients for xenotransplantation and were especially valuable for human stem cell assay. To elucidate the mechanisms involved in the superior engraftment rate in NOD/SCID/gamma(c)(null) mice, cytolkine production of spleen cells stimulated with Listeria monocytogenes antigens was compared among these 3 strains of mice. The interferon-gamma production from dendritic cells from the NOD/SCID/gamma(c)(null) mouse spleen was significantly suppressed in comparison with findings in 2 other strains of mice. It is suggested that multiple immunological dysfunctions, including cytokine production capability, in addition to functional incompetence of T, B, and NK cells, may lead to the high engraftment levels of xenograft in NOD/SCID/gamma(c)(null) mice. (C) 2002 by The American Society of Hematology.
引用
收藏
页码:3175 / 3182
页数:8
相关论文
共 50 条
  • [1] Establishment and characterization of in vivo human tumor models in the NOD/SCID/γcnull mouse
    Fujii, Etsuko
    Suzuki, Masami
    Matsubara, Koichi
    Watanabe, Miho
    Chen, Yu Jau
    Adachi, Kenji
    Ohnishi, Yasuyuki
    Tanigawa, Manabu
    Tsuchiya, Masayuki
    Tamaoki, Norikazu
    PATHOLOGY INTERNATIONAL, 2008, 58 (09) : 559 - 567
  • [2] Differentiation and functional maturation of human lymphocytes from hematopoietic stem cells in NOD/SCID γcnull mouse.
    Hiramatsu, H
    Heike, T
    Katamura, K
    Ito, M
    Ueyama, Y
    Nakahata, T
    BLOOD, 2002, 100 (11) : 609A - 609A
  • [4] MULTIPLE IMMUNE DEFECTS OF THE NOD/LTSZ-SCID/SCID MOUSE FACILITATE HUMAN HEMATOPOIETIC ENGRAFTMENT
    LOWRY, PA
    SHULTZ, LD
    GREINER, D
    TIARKS, CY
    RAO, SS
    RAMSHAW, H
    QUESENBERRY, PJ
    BLOOD, 1994, 84 (10) : A346 - A346
  • [5] A Nod Scid mouse model to study human prostate cancer
    C Bastide
    C Bagnis
    P Mannoni
    J Hassoun
    F Bladou
    Prostate Cancer and Prostatic Diseases, 2002, 5 : 311 - 315
  • [6] A Nod Scid mouse model to study human prostate cancer
    Bastide, C
    Bagnis, C
    Mannoni, P
    Hassoun, J
    Bladou, F
    PROSTATE CANCER AND PROSTATIC DISEASES, 2002, 5 (04) : 311 - 315
  • [7] Engraftment of NOD/SCID/γcnull mice with multilineage neoplastic cells from patients with juvenile myelomonocytic leukaemia
    Nakamura, Y
    Ito, M
    Yamamoto, T
    Yan, XY
    Yagasaki, H
    Kamachi, Y
    Kudo, K
    Kojima, S
    BRITISH JOURNAL OF HAEMATOLOGY, 2005, 130 (01) : 51 - 57
  • [8] Migration and NOD/SCID mouse engraftment of mesenchymal progenitor cells (MPC):: comparison with haematopoietic progenitor cells
    Rüster, B
    Grace, B
    Bistrian, R
    Seitz, O
    Henschler, R
    BONE MARROW TRANSPLANTATION, 2004, 33 : S85 - S85
  • [9] Characterization of the Hairless NOD/SCID Mouse Model
    Williams, S. V.
    Wildt, S. J.
    Brooks, A. I.
    Franklin, C. L.
    Livingston, B.
    Wiedmeyer, C. E.
    Cooper, D. M.
    JOURNAL OF THE AMERICAN ASSOCIATION FOR LABORATORY ANIMAL SCIENCE, 2010, 49 (05): : 737 - 737
  • [10] Destruction of human islets by human leukocytes in a new NOD scid mouse model
    Gerling, IC
    Ali, C
    Boehm, PE
    Fraga, DW
    Gaber, AO
    Saba, C
    DIABETES, 2001, 50 : A411 - A411