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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
来源:
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)
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页码:3543 / 3553
页数:11
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