Muller-Sieburg Christa E, Sieburg Hans B
Sidney Kimmel Cancer Center, 10835 Road to the Cure, San Diego, California 92112, USA.
Curr Opin Hematol. 2006 Jul;13(4):243-8. doi: 10.1097/01.moh.0000231421.00407.65.
Hematopoietic stem cells are functionally heterogeneous even when isolated as phenotypically homogenous populations. How this heterogeneity is generated is incompletely understood. Several models have been formulated to explain the generation of diversity. All of these assume the existence of a single type of hematopoietic stem cell that generates heterogeneous daughter stem cells in response to extrinsic or intrinsic (stochastic) signals. This view has encouraged the idea that stem cells can be instructed to adapt their function. Newer data, however, challenge this concept. Here, we summarize these findings and discuss their implication for applications of stem cells.
Hematopoietic stem cells that differ in function have been documented during development and within the adult stem cell compartment. The differences in function are stably inherited to daughter stem cells when these cells proliferate to self-renew. Collectively, the data show that the adult stem cell compartment consists of a limited number of distinct classes of stem cells.
The most important stem cell functions, including self-renewal and differentiation capacity, are preprogrammed through epigenetic or genetic mechanisms. Thus, stem cells are much more predictable than previously thought. Changes in the stem cell compartment through disease or aging can be interpreted as shifts in its clonal composition, rather than a modification of individual hematopoietic stem cells.
造血干细胞即使作为表型均一的群体分离出来,其功能也是异质性的。这种异质性是如何产生的尚未完全了解。已经提出了几种模型来解释多样性的产生。所有这些模型都假定存在一种单一类型的造血干细胞,它会响应外在或内在(随机)信号产生异质性的子代干细胞。这种观点促使人们认为干细胞可以被引导来调整其功能。然而,最新数据对这一概念提出了挑战。在这里,我们总结这些发现并讨论它们对干细胞应用的意义。
在发育过程中和成体干细胞区室中,已经记录到功能不同的造血干细胞。当这些细胞增殖进行自我更新时,其功能差异会稳定地遗传给子代干细胞。总体而言,数据表明成体干细胞区室由有限数量的不同类别的干细胞组成。
包括自我更新和分化能力在内的最重要的干细胞功能是通过表观遗传或遗传机制预先编程的。因此,干细胞比以前认为的更具可预测性。疾病或衰老导致的干细胞区室变化可以解释为其克隆组成的转变,而不是单个造血干细胞的改变。