The origins of the identification and isolation of hematopoietic stem cells, and their capability to induce donor-specific transplantation tolerance and treat autoimmune diseases

被引:288
作者
Weissman, Irving L. [1 ,2 ,3 ,4 ]
Shizuru, Judith A. [5 ]
机构
[1] Stanford Univ, Med Ctr, Stanford Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94304 USA
[2] Stanford Univ, Med Ctr, Ludwig Ctr Canc Stem Cell Res & Med, Stanford, CA 94304 USA
[3] Stanford Univ, Med Ctr, Dept Pathol, Stanford, CA 94304 USA
[4] Stanford Univ, Med Ctr, Dept Dev Biol, Stanford, CA 94304 USA
[5] Stanford Univ, Med Ctr, Dept Med, Div Blood & Marrow Transplantat, Stanford, CA 94304 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1182/blood-2008-08-078220
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Advances in the understanding of the cells of the hematopoietic system have provided a rich basis for improving clinical hematopoietic cell transplants; finding and using proteins and molecules to amplify or suppress particular blood cell types; understanding the stepwise progression of preleukemic stages leading first to chronic myeloid disorders, then the emergence of acute blastic leukemias; and treating malignant and nonmalignant diseases with cell subsets. As a result of intense scientific investigation, hematopoietic stem cells (HSCs) have been isolated and their key functional characteristics revealed-self-renewal and multilineage differentiation. These characteristics are now found to be present in all tissue/organ stem cell studies, and even in the analysis of pluripotent embryonic, nuclear transfer, and induced pluripotent stem cells. Studies on HSC have identified hematopoiesis as one of the best systems for studying developmental cell lineages and as the best for understanding molecular changes in cell fate decision-making and for finding preclinical and clinical platforms for tissue and organ replacement, regeneration, and oncogenesis. Here we review the steps, from our viewpoint, that led to HSC isolation and its importance in self-nonself immune recognition. (Blood. 2008; 112: 3543-3553)
引用
收藏
页码:3543 / 3553
页数:11
相关论文
共 129 条
[1]   AN ATTEMPT TO PRODUCE PRE-T CELL HYBRIDOMAS AND TO IDENTIFY THEIR ANTIGENS [J].
AIHARA, Y ;
BUHRING, HJ ;
AIHARA, M ;
KLEIN, J .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1986, 16 (11) :1391-1399
[2]   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
[3]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[4]   Telomerase is required to slow telomere shortening and extend replicative lifespan of HSCs during serial transplantation [J].
Allsopp, RC ;
Morin, GB ;
DePinho, R ;
Harley, CB ;
Weissman, IL .
BLOOD, 2003, 102 (02) :517-520
[5]   Common lymphoid progenitors rapidly engraft and protect against lethal murine cytomegalovirus infection after hematopoietic stem cell transplantation [J].
Arber, C ;
BitMansour, A ;
Sparer, TE ;
Higgins, JP ;
Mocarski, ES ;
Weissman, IL ;
Shizuru, JA ;
Brown, JMY .
BLOOD, 2003, 102 (02) :421-428
[6]   Stem cell-like glioma cells promote tumor angiogenesis through vascular endothelial growth factor [J].
Bao, Shideng ;
Wu, Qiulian ;
Sathornsumetee, Sith ;
Hao, Yueling ;
Li, Zhizhong ;
Hjelmeland, Anita B. ;
Shi, Oing ;
McLendon, Roger E. ;
Bigner, Darell D. ;
Rich, Jeremy N. .
CANCER RESEARCH, 2006, 66 (16) :7843-7848
[7]   IL-15-mediated induction of LFA-1 is a late step required for cytotoxic differentiation of human NK cells from CD34+Lin- bone marrow cells [J].
Barao, I ;
Hudig, D ;
Ascensao, JL .
JOURNAL OF IMMUNOLOGY, 2003, 171 (02) :683-690
[8]   ISOLATION OF A CANDIDATE HUMAN HEMATOPOIETIC STEM-CELL POPULATION [J].
BAUM, CM ;
WEISSMAN, IL ;
TSUKAMOTO, AS ;
BUCKLE, AM ;
PEAULT, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) :2804-2808
[9]   CYTOLOGICAL DEMONSTRATION OF CLONAL NATURE OF SPLEEN COLONIES DERIVED FROM TRANSPLANTED MOUSE MARROW CELLS [J].
BECKER, AJ ;
TILL, JE ;
MCCULLOCH, EA .
NATURE, 1963, 197 (486) :452-&
[10]   Prevention of type 1 diabetes with major histocompatibility complex-compatible and nonmarrow ablative hematopoietic stem cell transplants [J].
Beilhack, GF ;
Landa, RR ;
Masek, MA ;
Shizuru, JA .
DIABETES, 2005, 54 (06) :1770-1779