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Stem cell biology is population biology: differentiation of hematopoietic multipotent progenitors to common lymphoid and myeloid progenitors

机译:干细胞生物学是种群生物学:将造血多能祖细胞分化为常见的淋巴和髓样祖细胞

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The hematopoietic stem cell (HSC) system is a demand control system, with the demand coming from the organism, since the products of the common myeloid and lymphoid progenitor (CMP, CLP respectively) cells are essential for activity and defense against disease. We show how ideas from population biology (combining population dynamics and evolutionary considerations) can illuminate the feedback control of the HSC system by the fully differentiated products, which has recently been verified experimentally. We develop models for the penultimate differentiation of HSC Multipotent Progenitors (MPPs) into CLP and CMP and introduce two concepts from population biology into stem cell biology. The first concept is the Multipotent Progenitor Commitment Response (MPCR) which is the probability that a multipotent progenitor cell follows a CLP route rather than a CMP route. The second concept is the link between the MPCR and a measure of Darwinian fitness associated with organismal performance and the levels of differentiated lymphoid and myeloid cells. We show that many MPCRs are consistent with homeostasis, but that they will lead to different dynamics of cells and signals following a wound or injury and thus have different consequences for Darwinian fitness. We show how coupling considerations of life history to dynamics of the HSC system and its products allows one to compute the selective pressures on cellular processes. We discuss ways that this framework can be used and extended.
机译:造血干细胞(HSC)系统是一种需求控制系统,其需求来自生物体,因为普通髓样和淋巴祖细胞(分别为CMP,CLP)的细胞产物对于活性和防御疾病至关重要。我们展示了来自种群生物学的思想(结合了种群动态和进化方面的考虑)如何能够通过完全分化的产品阐明HSC系统的反馈控制,该产品最近已通过实验验证。我们开发了HSC多能祖细胞(MPP)倒数第二种分化为CLP和CMP的模型,并将种群生物学中的两个概念引入干细胞生物学。第一个概念是多能祖细胞承诺反应(MPCR),它是多能祖细胞遵循CLP路径而不是CMP路径的概率。第二个概念是MPCR与与机体性能以及分化的淋巴和髓样细胞水平相关的达尔文适应性度量之间的联系。我们显示,许多MPCR与体内稳态相一致,但是它们会导致伤口或受伤后细胞和信号的动态变化,因此对达尔文的适应性具有不同的后果。我们展示了如何将生命史与HSC系统及其产品动力学联系起来,从而能够计算出细胞过程的选择性压力。我们讨论了可以使用和扩展此框架的方式。

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