Molecular imaging using labeled donor tissues reveals patterns of engraftment, rejection, and survival in transplantation

被引:80
作者
Cao, YA
Bachmann, MH
Beilhack, A
Yang, Y
Tanaka, M
Swijnenburg, RJ
Reeves, R
Taylor-Edwards, C
Schulz, S
Doyle, TC
Fathman, CG
Robbins, RC
Herzenberg, LA
Negrin, RS
Contag, CH
机构
[1] Stanford Univ, Sch Med, Dept Pediat Radiol & Microbiol & Immunol, Stanford, CA USA
[2] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Program Immunol, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, Dept Cardiothorac Surg, Stanford, CA 94305 USA
关键词
molecular imaging; transplantation; tissue regeneration; stem cells;
D O I
10.1097/01.TP.0000164347.50559.A3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tissue regeneration and transplantation of solid organs involve complex processes that can only be studied in the context of the living organism, and methods of analyzing these processes in vivo are essential for development of effective transplantation and regeneration procedures. We utilized in vivo bioluminescence imaging (BLI) to noninvasively visualize engraftment, survival, and rejection of transplanted tissues from a transgenic donor mouse that constitutively expresses luciferase. Dynamic early events of hematopoietic reconstitution were accessible and engraftment from as few as 200 transplanted whole bone marrow (BM) cells resulted in bioluminescent foci in lethally irradiated, syngeneic recipients. The transplantation of autologous pancreatic Langerhans islets and of allogeneic heart revealed the tempo of transplant degeneration or immune rejection over time. This imaging approach is sensitive and reproducible, permits study of the dynamic range of the entire process of transplantation, and will greatly enhance studies across various disciplines involving transplantation.
引用
收藏
页码:134 / 139
页数:6
相关论文
共 20 条
  • [1] Shifting foci of hematopoiesis during reconstitution from single stem cells
    Cao, YA
    Wagers, AJ
    Beilhack, A
    Dusich, J
    Bachmann, MH
    Negrin, RS
    Weissman, IL
    Contag, CH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (01) : 221 - 226
  • [2] CHEN J, 2004, CURRENT MED CHEM IMM, V4, P301
  • [3] Visualizing gene expression in living mammals using a bioluminescent reporter
    Contag, CH
    Spilman, SD
    Contag, PR
    Oshiro, M
    Eames, B
    Dennery, P
    Stevenson, DK
    Benaron, DA
    [J]. PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1997, 66 (04) : 523 - 531
  • [4] Photonic detection of bacterial pathogens in living hosts
    Contag, CH
    Contag, PR
    Mullins, JI
    Spilman, SD
    Stevenson, DK
    Benaron, DA
    [J]. MOLECULAR MICROBIOLOGY, 1995, 18 (04) : 593 - 603
  • [5] Bioluminescent indicators in living mammals
    Contag, PR
    Olomu, IN
    Stevenson, DK
    Contag, CH
    [J]. NATURE MEDICINE, 1998, 4 (02) : 245 - 247
  • [6] PRIMARILY VASCULARIZED ALLOGRAFTS OF HEARTS IN MICE - ROLE OF H-2D, H-2K, AND NON-H-2 ANTIGENS IN REJECTION
    CORRY, RJ
    WINN, HJ
    RUSSELL, PS
    [J]. TRANSPLANTATION, 1973, 16 (04) : 343 - 350
  • [7] Analysis of the aphthovirus 2A/2B polyprotein 'cleavage' mechanism indicates not a proteolytic reaction, but a novel translational effect: a putative ribosomal 'skip'
    Donnelly, MLL
    Luke, G
    Mehrotra, A
    Li, XJ
    Hughes, LE
    Gani, D
    Ryan, MD
    [J]. JOURNAL OF GENERAL VIROLOGY, 2001, 82 : 1013 - 1025
  • [8] Revealing lymphoma growth and the efficacy of immune cell therapies using in vivo bioluminescence imaging
    Edinger, M
    Cao, YA
    Verneris, MR
    Bachmann, MH
    Contag, CH
    Negrin, RS
    [J]. BLOOD, 2003, 101 (02) : 640 - 648
  • [9] Generating green fluorescent mice by germline transmission of green fluorescent ES cells
    Hadjantonakis, AK
    Gertsenstein, M
    Ikawa, M
    Okabe, M
    Nagy, A
    [J]. MECHANISMS OF DEVELOPMENT, 1998, 76 (1-2) : 79 - 90
  • [10] Lejon K, 1999, J IMMUNOL, V163, P5708