Functional characterization of hematopoietic stem cells in the spleen

被引:80
作者
Morita, Yohei [2 ]
Iseki, Akiko [2 ]
Okamura, Satoshi [2 ]
Suzuki, Sachie [2 ]
Nakauchi, Hiromitsu [2 ]
Ema, Hideo [1 ]
机构
[1] Univ Tokyo, Lab Dev Stem Cell Biol, Ctr Stem Cell & Regenerat Med, Inst Med Sci,Minato Ku, Tokyo 1088639, Japan
[2] Univ Tokyo, Div Stem Cell Therapy, Tokyo 1088639, Japan
关键词
BONE-MARROW NICHE; COMPETITIVE REPOPULATION; LINEAGE COMMITMENT; IDENTIFICATION; QUIESCENCE; PLACENTA; ASSAY; MICE;
D O I
10.1016/j.exphem.2010.12.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Hematopoietic stem cells (HSCs) reside in both bone marrow (BM) and spleen in adult mice. However, whether BM and spleen HSCs are functionally similar is not known. Spleen HSCs were compared with BM HSCs by various assays. Materials and Methods. Whole BM and spleen cells were quantitatively analyzed by competitive repopulation. Single-cell transplantation was performed with HSCs purified from BM and spleen. A parabiosis model was used to distinguish organ-specific HSCs from circulating HSCs. The cell cycle was analyzed with pyronin Y staining and bromodeoxyuridine uptake. Results. Repopulating and self-renewal potentials were similar on a clonal basis between BM and spleen HSCs, whereas the HSC frequency in the spleen was significantly lower than that in the BM. Analysis of parabiotic mice suggested that most HSCs are long-term residents in each organ. Cell-cycle analysis revealed that spleen HSCs cycle twice as frequently as do BM HSCs, suggesting that G(0) phase length is longer in BM HSCs than in spleen HSCs. The cycling difference between BM and spleen HSCs was also observed in mice that had been reconstituted with BM or spleen cells, suggesting that HSC quiescence is regulated in an organ-specific manner. Conclusions. Spleen HSCs and BM HSCs are functionally similar, but their cycling behaviors differ. (C) 2011 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc.
引用
收藏
页码:351 / 359
页数:9
相关论文
共 32 条
[11]   Adult mouse hematopoietic stem cells: purification and single-cell assays [J].
Ema, Hideo ;
Morita, Yohei ;
Yamazaki, Satoshi ;
Matsubara, Azusa ;
Seita, Jun ;
Tadokoro, Yuko ;
Kondo, Hiroyoshi ;
Takano, Hina ;
Nakauchi, Hiromitsu .
NATURE PROTOCOLS, 2006, 1 (06) :2979-2987
[12]   The placenta is a niche for hematopoietic stem cells [J].
Gekas, C ;
Dieterlen-Lièvre, F ;
Orkin, SH ;
Mikkola, HKA .
DEVELOPMENTAL CELL, 2005, 8 (03) :365-375
[13]  
HARRISON DE, 1993, EXP HEMATOL, V21, P206
[14]  
HARRISON DE, 1994, BLOOD, V83, P3146
[15]   Uncertainty in the niches that maintain haematopoietic stem cells [J].
Kiel, Mark J. ;
Morrison, Sean J. .
NATURE REVIEWS IMMUNOLOGY, 2008, 8 (04) :290-301
[16]   SLAM family receptors distinguish hematopoietic stem and progenitor cells and reveal endothelial niches for stem cells [J].
Kiel, MJ ;
Yilmaz, ÖH ;
Iwashita, T ;
Yilmaz, OH ;
Terhorst, C ;
Morrison, SJ .
CELL, 2005, 121 (07) :1109-1121
[17]  
LAJTHA LG, 1979, DIFFERENTIATION, V14, P23, DOI 10.1111/j.1432-0436.1979.tb01007.x
[18]   Mesenchymal and haematopoietic stem cells form a unique bone marrow niche [J].
Mendez-Ferrer, Simon ;
Michurina, Tatyana V. ;
Ferraro, Francesca ;
Mazloom, Amin R. ;
MacArthur, Ben D. ;
Lira, Sergio A. ;
Scadden, David T. ;
Ma'ayan, Avi ;
Enikolopov, Grigori N. ;
Frenette, Paul S. .
NATURE, 2010, 466 (7308) :829-U59
[19]  
Metcalf D., 1971, HAEMOPOIETIC CELLS
[20]   Prospective identification, isolation, and systemic transplantation of multipotent mesenchymal stem cells in murine bone marrow [J].
Morikawa, Satoru ;
Mabuchi, Yo ;
Kubota, Yoshiaki ;
Nagai, Yasuo ;
Niibe, Kunimichi ;
Hiratsu, Emi ;
Suzuki, Sadafumi ;
Miyauchi-Hara, Chikako ;
Nagoshi, Narihito ;
Sunabori, Takehiko ;
Shimmura, Shigeto ;
Miyawaki, Atsushi ;
Nakagawa, Taneaki ;
Suda, Toshio ;
Okano, Hideyuki ;
Matsuzaki, Yumi .
JOURNAL OF EXPERIMENTAL MEDICINE, 2009, 206 (11) :2483-2496