Plasticity of hematopoietic stem cells and cellular memory

被引:13
作者
Avots, A [1 ]
Harder, F [1 ]
Schmittwolf, C [1 ]
Petrovic, S [1 ]
Müller, AM [1 ]
机构
[1] Univ Wurzburg, Inst Med Strahlenkunde & Zellforsch, Stem Cells Grp, D-97078 Wurzburg, Germany
关键词
D O I
10.1034/j.1600-065X.2002.18702.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Stem cell systems represent an effective and powerful approach for tissue development and regeneration of diverse tissue types. Common and defining features of these exceptional cells are the capacity for self-renewal and the potential for differentiation into multiple mature cell types. Recently, surprising new observations have indicated that stem cells isolated from one adult tissue can also give rise to mature cells of other cell lineages, irrespective of classical germ layer designations. This discovery has resulted in quantum leaps in both scientific knowledge and the potential applications of stem cells. The new findings contradict central dogmas of commitment and differentiation of stem and progenitor cells. However, the true potential of somatic stem cells is just emerging and the new findings have to be defined more fully and integrated into a unifying model of stem cell potential and behavior. Here we analyze the developmental potential of hematopoietic stem cells of mouse and man following their injection into the murine preimplantation blastocyst, an environment that allows the development of all cell lineages. In addition, we discuss the emerging lines of evidence of the developmental plasticity of hematopoietic and other somatic stem cells and consider how cellular memory of transcriptional states is established and may be potentially involved in this phenomenon.
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页码:9 / 21
页数:13
相关论文
共 91 条
[11]   The Polycomb group - no longer an exclusive club? [J].
Brock, HW ;
van Lohuizen, M .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2001, 11 (02) :175-181
[12]   Synergistic regulation of human beta-globin gene switching by locus control region elements HS3 and HS4 [J].
Bungert, J ;
Dave, U ;
Lim, KC ;
Lieuw, KH ;
Shavit, JA ;
Liu, QH ;
Engel, JD .
GENES & DEVELOPMENT, 1995, 9 (24) :3083-3096
[13]   Hematopoietic development: a balancing act [J].
Cantor, AB ;
Orkin, SH .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2001, 11 (05) :513-519
[14]   The amino terminus of the mixed lineage leukemia protein (MLL) promotes cell cycle arrest and monocytic differentiation [J].
Caslini, C ;
Shilatifard, A ;
Yang, LP ;
Hess, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (06) :2797-2802
[15]  
CIVIN CI, 1984, J IMMUNOL, V133, P157
[16]   Generalized potential of adult neural stem cells [J].
Clarke, DL ;
Johansson, CB ;
Wilbertz, J ;
Veress, B ;
Nilsson, E ;
Karlström, H ;
Lendahl, U ;
Frisén, J .
SCIENCE, 2000, 288 (5471) :1660-1663
[17]  
Core N, 1997, DEVELOPMENT, V124, P721
[18]   Association of SET domain and myotubularin-related proteins modulates growth control [J].
Cui, XM ;
De Vivo, I ;
Slany, R ;
Miyamoto, A ;
Firestein, R ;
Cleary, ML .
NATURE GENETICS, 1998, 18 (04) :331-337
[19]   Growth stimulation of primary B cell precursors by the anti-phosphatase Sbf1 [J].
De Vivo, I ;
Cui, XM ;
Domen, J ;
Cleary, ML .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (16) :9471-9476
[20]   ESTABLISHMENT IN CULTURE OF PLURIPOTENTIAL CELLS FROM MOUSE EMBRYOS [J].
EVANS, MJ ;
KAUFMAN, MH .
NATURE, 1981, 292 (5819) :154-156