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正常和白血病造血过程中克隆扩增期间的干细胞更新与分化。

Stem cell renewal and determination during clonal expansion in normal and leukaemic haemopoiesis.

作者信息

McCulloch E A

机构信息

Department of Medical Biophysics, the University of Toronto, Canada.

出版信息

Cell Prolif. 1993 Sep;26(5):399-425. doi: 10.1111/j.1365-2184.1993.tb00129.x.

Abstract

Normal haemopoiesis is a cellular hierarchy headed by pluripotent stem cells capable of both self renewal and, after determination, the generation of differentiating lineages that end in terminal functional cells. The role of stem cells is crucial because only these have the capacity to generate clonal populations during development or after injury. During clonal expansion the cells are affected by many sets of receptors and ligands. These belong to at least two classes: one consists of growth factors that bind cell surface receptors and initiate signalling events; the other class contains receptors which act as ligand-dependent transcription factors such as the intracellular steroid superfamily. In spite of this elaborate regulatory apparatus, control during clonal expansion is lax, perhaps stochastic, as evident from the great heterogeneity disclosed by examining the cellular compositions of haemopoietic clones. It may be that the large number of signals impinging on binary possible outcomes (for example self-renewal or determination) serve to set probabilities rather than to determine outcomes. In leukaemia, many of the features of normal haemopoiesis are retained. The disease begins as transformations in normal stem cells; after additional leukaemogenic events clonal expansion yields malignant populations which are clonal in each affected individual. These dominant clonal populations retain the hierarchical organization found in the normal, the major difference is that post-deterministic divisions in leukaemia yield descendants that retain primitive (blast) morphology although proliferative capacity is lost. In acute myeloblastic leukaemia (AML) cell culture methods are available that permit the measurement of clonogenic blast stem cells. These methods have shown that regulatory mechanisms active in normal haemopoiesis are retained in AML, including lax regulation during clonal expansion. The biological features of blast stems cells displayed by the culture technique reflect in part, events in vivo, as associations have been found between results in cell culture and clinical outcome. Thus, study of leukaemic populations provides a challenge for basic science and an opportunity for successful application in control of disease.

摘要

正常造血是一个细胞层次结构,由多能干细胞主导,这些干细胞既能自我更新,又能在定向分化后产生最终形成终末功能细胞的分化谱系。干细胞的作用至关重要,因为只有它们有能力在发育过程中或损伤后产生克隆群体。在克隆扩增过程中,细胞会受到多组受体和配体的影响。这些至少可分为两类:一类是与细胞表面受体结合并启动信号转导事件的生长因子;另一类包含作为配体依赖性转录因子的受体,如细胞内类固醇超家族。尽管有这种精细的调节机制,但克隆扩增过程中的控制较为宽松,可能是随机的,这从检查造血克隆的细胞组成所揭示的巨大异质性中可以明显看出。也许大量作用于二元可能结果(例如自我更新或定向分化)的信号是用来设定概率而非决定结果。在白血病中,正常造血的许多特征得以保留。疾病始于正常干细胞的转化;在发生其他致白血病事件后,克隆扩增产生恶性群体,每个受影响个体中的这些群体都是克隆性的。这些占主导地位的克隆群体保留了正常情况下的层次结构,主要区别在于白血病中定向分化后的分裂产生的后代虽失去增殖能力,但仍保留原始(母细胞)形态。在急性髓细胞白血病(AML)中,可以使用细胞培养方法来测量克隆形成母细胞干细胞。这些方法表明,正常造血中活跃的调节机制在AML中得以保留,包括克隆扩增过程中的宽松调节。培养技术所显示的母细胞干细胞的生物学特征部分反映了体内情况,因为在细胞培养结果与临床结果之间已发现相关性。因此,白血病群体的研究对基础科学提出了挑战,也为成功应用于疾病控制提供了机会。

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