The topologic and chronologic patterns of hematopoietic cell seeding in host femoral bone marrow after transplantation

被引:14
作者
Askenasy, N
Stein, Y
Yaniv, I
Farkas, DL
机构
[1] Schneiders Childrens Med Ctr, Ctr Pediat Hematol Oncol, Frankel Lab Bone Marrow Transplantat, Dept Pediat Hematol Oncol, IL-49202 Petah Tiqwa, Israel
[2] Cedars Sinai Med Ctr, Dept Surg, Minimally Invas Surg Technol Inst, Los Angeles, CA 90048 USA
关键词
hematopoietic cell seeding; femoral bone marrow; in vivo microscopy; PKH membrane linkers; STEM-CELLS; IN-VIVO; SPATIAL DISTRIBUTIONS; PROGENITOR CELLS; SHORT-TERM; CFU-S; ENGRAFTMENT; ADHESION; MICE;
D O I
10.1016/S1083-8791(03)00150-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The early stages of homing, seeding, and engraftment of hematopoietic stem and progenitor cells are poorly characterized. We have developed an optical technique that allows in vivo tracking of transplanted, fluorescent-tagged cells in the host femurs. In this study we used fluorescence microscopy to monitor the topologic and chronologic patterns of hematopoietic cell seeding in the femoral bone marrow (BM) of mice. PKH-labeled cells homed to the femur within minutes after injection into a peripheral vein. Most cells drifted within the marrow space and gradually seeded in clusters close to the endosteal surface of the epiphyseal cortex. Three days after transplantation 85% to 94% (14%) of PKH-labeled cells in the femoral marrow were located within 100 mum of the epiphyseal bone surface (P < .001 versus the more central cells), whereas labeled cells were absent in the femoral diaphysis. Primary seeding of juxtaendosteal, epiphyseal marrow occurred independently of recipient conditioning (myeloablated and nonconditioned hosts), donor-recipient antigen disparity, or the phenotype of the injected cells (whole BM and lineage-negative cells) and was consistently observed in secondary recipients of BM-homed cells. Seeding in regions close to the epiphyseal bone was also observed in freshly excised femurs perfused ex vivo and in femurs assessed without prior placement of optical windows, indicating that the site of primary seeding was not affected by surgical placement of optical windows. Four to 5 days after transplantation, cellular clusters appeared in the more central regions of the epiphyses and in the diaphyses. Centrally located cells showed decreased PKH fluorescence, suggesting that they were progeny of the seeding cells, and brightly fluorescent cells (quiescent first-generation seeding cells) were observed close to the bone surface for as long as 24 days after transplantation. These data indicate that the periphery of the femoral marrow hosts primary seeding and that quiescent cells continue to reside in the periphery for weeks and do not divide. The site of proliferation of transplanted cells is the center of the marrow space. (C) 2003 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:496 / 504
页数:9
相关论文
共 33 条
[1]  
Aiuti A, 1998, EXP HEMATOL, V26, P143
[2]   In vivo imaging of gene and cell therapies [J].
Allport, JR ;
Weissleder, R .
EXPERIMENTAL HEMATOLOGY, 2001, 29 (11) :1237-1246
[3]   Transplanted hematopoietic cells seed in clusters in recipient bone marrow in vivo [J].
Askenasy, N ;
Zorina, T ;
Farkas, DL ;
Shalit, I .
STEM CELLS, 2002, 20 (04) :301-310
[4]   In vivo imaging studies of the effect of recipient conditioning, donor cell phenotype and antigen disparity on homing of haematopoietic cells to the bone marrow [J].
Askenasy, N ;
Farkas, DL .
BRITISH JOURNAL OF HAEMATOLOGY, 2003, 120 (03) :505-515
[5]   Antigen barriers or available space do not restrict in situ adhesion of hemopoietic cells to bone marrow stroma [J].
Askenasy, N ;
Farkas, DL .
STEM CELLS, 2002, 20 (01) :80-85
[6]   Localized bone marrow transplantation leads to skin allograft acceptance in nonmyeloablated recipients: Comparison of intra-bone marrow and isolated limb perfusion [J].
Askenasy, N .
STEM CELLS, 2002, 20 (01) :86-93
[7]   Optical imaging of PKH-labeled hematopoietic cells in recipient bone marrow in vivo [J].
Askenasy, N ;
Farkas, DL .
STEM CELLS, 2002, 20 (06) :501-513
[8]   Donor stem cells home to marrow efficiently and contribute to short- and long-term hematopoiesis after low-cell-dose unconditioned bone marrow transplantation [J].
Bubnic, SJ ;
Keating, A .
EXPERIMENTAL HEMATOLOGY, 2002, 30 (06) :606-611
[9]   Bone marrow cell trafficking following intravenous administration [J].
Cui, JS ;
Wahl, RL ;
Shen, TL ;
Fisher, SJ ;
Recker, E ;
Ginsburg, D ;
Long, MW .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 107 (04) :895-902
[10]  
El-Badri NS, 1998, EXP HEMATOL, V26, P110