Advances in hematopoietic stem cell research through mouse genetics

被引:7
作者
Miller, Alison
Van Zant, Gary
机构
[1] Univ Kentucky, Med Ctr, Dept Physiol, Lexington, KY USA
[2] Univ Kentucky, Med Ctr, Dept Internal Med, Lexington, KY USA
关键词
bone marrow transplant; differentiation; hematopoietic; stem cell; microarray; self-renewal;
D O I
10.1097/01.moh.0000231416.25956.35
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Successful bone marrow transplantation involves migration of hematopoietic stem cells through the blood, entering the extravascular,hematopoietic cords, lodging in the proper niche, and expanding and differentiating to produce large numbers of mature: cells - all without depletion of the stem cell pool. An additional variable in these processes is the age of both the donor bone marrow and the recipient. Basic stem cell biology and transplant biology aim to uncover the molecular mechanisms controlling these processes. Recent findings Mouse genetics is a frequently used tool that allows dissection of individual pathways that influence properties of hematopoietic stem cells. Recently, the conception of a niche has been expanded to include evidence for a vascular and an endosteal niche. Additionally, hematopoietic stem cell interactions within the niche have been further defined, documenting the importance of cell cycle, cell adhesion, response to cytokine stimulation and age-dependent functional changes. A new model for hematopoietic stem cell that supports the hypothesis that stem cell aging partially due to an accumulation of DNA damage leading to exhaustion. Summary This review focuses on the last year's progress using mouse genetics as' a tool to study intrinsic mechanisms of hematopoietic stem cell biology.
引用
收藏
页码:209 / 215
页数:7
相关论文
共 60 条
[1]   Hox regulation of normal and leukemic hematopoietic stem cells [J].
Abramovich, Carolina ;
Humphries, R. Keith .
CURRENT OPINION IN HEMATOLOGY, 2005, 12 (03) :210-216
[2]   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
[3]   A clonogenic common myeloid progenitor that gives rise to all myeloid lineages [J].
Akashi, K ;
Traver, D ;
Miyamoto, T ;
Weissman, IL .
NATURE, 2000, 404 (6774) :193-197
[4]   Transcriptional accessibility for genes of multiple tissues and hematopoietic lineages is hierarchically controlled during early hematopoiesis [J].
Akashi, K ;
He, X ;
Chen, J ;
Iwasaki, H ;
Niu, C ;
Steenhard, B ;
Zhang, JW ;
Haug, J ;
Li, LH .
BLOOD, 2003, 101 (02) :383-390
[5]   Ex vivo expansion of human hematopoietic stem cells by direct delivery of the HOXB4 homeoprotein [J].
Amsellem, S ;
Pflumio, F ;
Bardinet, D ;
Izac, B ;
Charneau, P ;
Romeo, PH ;
Dubart-Kupperschmitt, A ;
Fichelson, S .
NATURE MEDICINE, 2003, 9 (11) :1423-1427
[6]   HOXB4-induced expansion of adult hematopoietic stem cells ex vivo [J].
Antonchuk, J ;
Sauvageau, G ;
Humphries, RK .
CELL, 2002, 109 (01) :39-45
[7]  
BIJL J, 2005, BLOOD
[8]   Cell intrinsic defects in cytokine responsiveness of STAT5-deficient hematopoietic stem cells [J].
Bradley, HL ;
Hawley, TS ;
Bunting, KD .
BLOOD, 2002, 100 (12) :3983-3989
[9]   Hoxb4-deficient mice undergo normal hematopoietic development but exhibit a mild proliferation defect in hematopoietic stem cells [J].
Brun, ACM ;
Björnsson, JM ;
Magnusson, M ;
Larsson, N ;
Leveén, P ;
Ehinger, M ;
Nilsson, E ;
Karlsson, S .
BLOOD, 2004, 103 (11) :4126-4133
[10]   Reduced lymphomyeloid repopulating activity from adult bone marrow and fetal liver of mice lacking expression of STAT5 [J].
Bunting, KD ;
Bradley, HL ;
Hawley, TS ;
Moriggl, R ;
Sorrentino, BP ;
Ihle, JN .
BLOOD, 2002, 99 (02) :479-487