Role of N-cadherin in the regulation of hematopoietic stem cells in the bone marrow niche

被引:48
作者
Arai, Fumio [1 ]
Hosokawa, Kentaro [1 ]
Toyama, Hirofumi [1 ]
Matsumoto, Yoshiko [1 ]
Suda, Toshio [1 ]
机构
[1] Keio Univ, Sch Med, Dept Cell Differentiat, Sakaguchi Lab Dev Biol,Shinjuku Ku, Tokyo 1608582, Japan
来源
HEMATOPOIETIC STEM CELLS VIII | 2012年 / 1266卷
基金
日本学术振兴会;
关键词
N-cadherin; hematopoietic stem cells; niche; osteoblasts; ADHESION; MAINTENANCE; MICROENVIRONMENT; ACTIVATION; DEPEND;
D O I
10.1111/j.1749-6632.2012.06576.x
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Cell-cell and cell-extracellular matrix interactions between hematopoietic stem cells (HSCs) and their niches are critical for the maintenance of stem cell properties. Here, it is demonstrated that a cell adhesion molecule, N-cadherin, is expressed in hematopoietic stem/progenitor cells (HSPCs) and plays a critical role in the regulation of HSPC engraftment. Furthermore, overexpression of N-cadherin in HSCs promoted quiescence and preserved HSC activity during serial bone marrow (BM) transplantation (BMT). Inhibition of N-cadherin by the transduction of N-cadherin short hairpin (sh) RNA(shN-cad) reduced the lodgment of donor HSCs to the endosteal surface, resulting in a significant reduction in long-term engraftment. shN-cad-transduced cells were maintained in the spleen for six months after BMT, indicating that N-cadherin expression in HSCs is specifically required in the BM. These findings suggest that N-cadherin-mediated cell adhesion is functionally essential for the regulation of HSPC activities in the BM niche.
引用
收藏
页码:72 / 77
页数:6
相关论文
共 30 条
[1]
Constitutively active β-catenin promotes expansion of multipotent hematopoietic progenitors in culture [J].
Baba, Yoshihiro ;
Yokota, Takafumi ;
Spits, Hergen ;
Garrett, Karla P. ;
Hayashi, Shin-Ichi ;
Kincade, Paul W. .
JOURNAL OF IMMUNOLOGY, 2006, 177 (04) :2294-2303
[2]
Socializing with the neighbors: Stem cells and their niche [J].
Fuchs, E ;
Tumbar, T ;
Guasch, G .
CELL, 2004, 116 (06) :769-778
[3]
Cell adhesion: The molecular basis of tissue architecture and morphogenesis [J].
Gumbiner, BM .
CELL, 1996, 84 (03) :345-357
[4]
N-cadherin expression level distinguishes reserved versus primed states of hematopoietic stem cells [J].
Haug, Jeffrey S. ;
He, Xi C. ;
Grindley, Justin C. ;
Wunderlich, Joshua P. ;
Gaudenz, Karin ;
Ross, Jason T. ;
Paulson, Ariel ;
Wagner, Kathryn P. ;
Xie, Yucai ;
Zhu, Ruihong ;
Yin, Tong ;
Perry, John M. ;
Hembree, Mark J. ;
Redenbaugh, Erin P. ;
Radice, Glenn L. ;
Seidel, Christopher ;
Li, Linheng .
CELL STEM CELL, 2008, 2 (04) :367-379
[5]
Knockdown of N-cadherin suppresses the long-term engraftment of hematopoietic stem cells [J].
Hosokawa, Kentaro ;
Arai, Fumio ;
Yoshihara, Hiroki ;
Iwasaki, Hiroko ;
Nakamura, Yuka ;
Gomei, Yumiko ;
Suda, Toshio .
BLOOD, 2010, 116 (04) :554-563
[6]
Cadherin-Based Adhesion Is a Potential Target for Niche Manipulation to Protect Hematopoietic Stem Cells in Adult Bone Marrow [J].
Hosokawa, Kentaro ;
Arai, Fumio ;
Yoshihara, Hiroki ;
Iwasaki, Hiroko ;
Hembree, Mark ;
Yin, Tong ;
Nakamura, Yuka ;
Gomei, Yumiko ;
Takubo, Keiyo ;
Shiama, Haruko ;
Matsuoka, Sahoko ;
Li, Linheng ;
Suda, Toshio .
CELL STEM CELL, 2010, 6 (03) :194-198
[7]
Uncertainty in the niches that maintain haematopoietic stem cells [J].
Kiel, Mark J. ;
Morrison, Sean J. .
NATURE REVIEWS IMMUNOLOGY, 2008, 8 (04) :290-301
[8]
Lack of evidence that hematopoietic stem cells depend on N-cadherin-mediated adhesion to osteoblasts for their maintenance [J].
Kiel, Mark J. ;
Radice, Glenn L. ;
Morrison, Sean J. .
CELL STEM CELL, 2007, 1 (02) :204-217
[9]
Hematopoietic Stem Cells Do Not Depend on N-Cadherin to Regulate Their Maintenance [J].
Kiel, Mark J. ;
Acar, Melih ;
Radice, Glenn L. ;
Morrison, Sean J. .
CELL STEM CELL, 2009, 4 (02) :170-179
[10]
Activation of the canonical Wnt pathway leads to loss of hematopoietic stem cell repopulation and multilineage differentiation block [J].
Kirstetter, Peggy ;
Anderson, Kristina ;
Porse, Bo T. ;
Jacobsen, Sten Eirik W. ;
Nerlov, Claus .
NATURE IMMUNOLOGY, 2006, 7 (10) :1048-1056