Bunting Kevin D, Hawley Robert G
Hematopoiesis Department, Cell Therapy Research and Development, American Red Cross Holland Laboratory, 15601 Crabbs Branch Way, Rockville, MD 20855, USA.
ScientificWorldJournal. 2002 Apr 10;2:983-95. doi: 10.1100/tsw.2002.162.
Hematopoietic stem cells (HSCs) are the best studied of the tissue-specific stem cells. By definition, HSCs have long been regarded as restricted to formation of blood cells of both the lymphoid and myeloid lineages. HSCs residing in the bone marrow microenvironment have self-renewal capacity and can repopulate the hematopoietic system of irradiated transplant recipients for the lifetime of the individual. Therefore, HSCs are extremely important targets for gene therapy applications aimed toward the treatment of inherited and acquired blood disorders. However, recent studies have suggested that a subpopulation of HSCs may have the ability to contribute to diverse cell types such as hepatocytes, myocytes, and neuronal cells, especially following induced tissue damage. Preclinical amelioration of liver disease and myocardial infarcts by HSC-enriched bone marrow cell populations raises the possibility that HSC transplants have the potential to provide therapeutic benefit for a wide variety of diseases. These surprising findings contradict the dogma that adult stem cells are developmentally restricted. Extrapolation of these findings to the clinic will be facilitated by prospective identification of the stem cells that possess this developmental plasticity. Furthermore, characterization of the signaling pathways and molecular determinants regulating the remarkable transdifferentiation capacity of these stem cells may provide insight into novel approaches for modulating frequency of differentiative potential.
造血干细胞(HSCs)是组织特异性干细胞中研究最为深入的。根据定义,长期以来HSCs一直被认为局限于形成淋巴系和髓系血细胞。存在于骨髓微环境中的HSCs具有自我更新能力,并且能够在个体的一生中重新填充受辐射移植受体的造血系统。因此,HSCs是针对遗传性和获得性血液疾病治疗的基因治疗应用的极其重要的靶点。然而,最近的研究表明,HSCs的一个亚群可能有能力分化为多种细胞类型,如肝细胞、心肌细胞和神经细胞,特别是在诱导组织损伤后。富含HSC的骨髓细胞群体对肝脏疾病和心肌梗死的临床前改善提高了HSC移植有可能为多种疾病提供治疗益处的可能性。这些惊人的发现与成体干细胞在发育上受限的教条相矛盾。通过前瞻性鉴定具有这种发育可塑性的干细胞,将有助于将这些发现推广到临床。此外,对调节这些干细胞显著转分化能力的信号通路和分子决定因素的表征,可能为调节分化潜能频率的新方法提供见解。