Stem cell homing

被引:113
作者
Chute, John P. [1 ]
机构
[1] Duke Univ, Med Ctr, Div Cellular Therapy, Durham, NC 27710 USA
关键词
endothelial cells; hematopoiesis; homing; migration; stem cells;
D O I
10.1097/01.moh.0000245698.62511.3d
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Abbreviations Transplantation of hematopoietic stem cells is dependent upon the successful homing, engraftment and repopulation of stem cells in the bone marrow. Stem cell homing through the circulation to the bone marrow is the critical first step in this process. This review discusses the latest progress in defining the molecular processes underlying stem cell homing and the specialized niches where stem cells reside. Recent findings Over the past decade, remarkable advances have been made in characterizing the complex sequence of events involved in stem cell homing to the bone marrow. Specifically, the molecular basis of stem cell adhesion and rolling along bone marrow sinusoidal endothelial cells has been defined, and mechanisms underlying endothelial transmigration and enlodgement in bone marrow niches have now bean identified. The processes governing hematopoietic, stem cell homing to the bone marrow also regulate hematopoietic stem cell migration to extramedullary tissues and the metastasis of cancer stem cells. Improved understanding of these processes has catalyzed the development of therapies to facilitate stem cell mobilization for clinical purposes. Summary Several components of the essential process of stem cell homing have now been characterized. Cell adhesion molecules and their ligands, extracellular matrix components, chemokines, and specialized bone marrow niches all participate in the precise regulation of this process.
引用
收藏
页码:399 / 406
页数:8
相关论文
共 80 条
[1]   Stem cell engraftment at the endosteal niche is specified by the calcium-sensing receptor [J].
Center for Regenerative Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, United States ;
不详 ;
不详 ;
不详 ;
不详 ;
不详 .
Nature, 2006, 7076 (599-603) :599-603
[2]   Heterologous cells cooperate to augment stem cell migration, homing, and engraftment [J].
Adams, GB ;
Chabner, KT ;
Foxall, RB ;
Weibrecht, KW ;
Rodrigues, NP ;
Dombkowski, D ;
Fallon, R ;
Poznansky, MC ;
Scadden, DT .
BLOOD, 2003, 101 (01) :45-51
[3]   MODIFICATION OF X-RADIATION LETHALITY BY AUTOLOGOUS MARROW INFUSION IN DOGS [J].
ALPEN, EL ;
BAUM, SJ .
BLOOD, 1958, 13 (12) :1168-1175
[4]   Chemokine-mediated interaction of hematopoietic progenitors with the bone marrow vascular niche is required for thrombopoiesis [J].
Avecilla, ST ;
Hattori, K ;
Heissig, B ;
Tejada, R ;
Liao, F ;
Shido, K ;
Jin, DK ;
Dias, S ;
Zhang, F ;
Hartman, TE ;
Hackett, NR ;
Crystal, RG ;
Witte, L ;
Hicklin, DJ ;
Bohlen, P ;
Eaton, D ;
Lyden, D ;
de Sauvage, F ;
Rafii, S .
NATURE MEDICINE, 2004, 10 (01) :64-71
[5]  
AWIGDOR A, 2004, BLOOD, V104, P2981
[6]   Hematopoietic stem cells engraft in mice with absolute efficiency [J].
Benveniste, P ;
Cantin, C ;
Hyam, D ;
Iscove, NN .
NATURE IMMUNOLOGY, 2003, 4 (07) :708-713
[7]   Hierarchy of molecular-pathway usage in bone marrow homing and its shift by cytokines [J].
Bonig, H ;
Priestley, GV ;
Papayannopoulou, T .
BLOOD, 2006, 107 (01) :79-86
[8]   PTX-sensitive signals in bone marrow homing of fetal and adult hematopoietic progenitor cells [J].
Bonig, H ;
Priestley, GV ;
Nilsson, LM ;
Jiang, Y ;
Papayannopoulou, T .
BLOOD, 2004, 104 (08) :2299-2306
[9]   Cytokine treatment or accessory cells are required to initiate engraftment of purified primitive human hematopoietic cells transplanted at limiting doses into NOD/SCID mice [J].
Bonnet, D ;
Bhatia, M ;
Wang, JCY ;
Kapp, U ;
Dick, JE .
BONE MARROW TRANSPLANTATION, 1999, 23 (03) :203-209
[10]   CXCR4-transgene expression significantly improves marrow engraftment of cultured hematopoietic stem cells [J].
Brenner, S ;
Whiting-Theobald, N ;
Kawai, T ;
Linton, GF ;
Rudikoff, AG ;
Choi, U ;
Ryser, MF ;
Murphy, PM ;
Sechler, JMG ;
Malech, HL .
STEM CELLS, 2004, 22 (07) :1128-1133