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Hematopoiesis and Stem Cells: Kinetics of normal hematopoietic stem and progenitor cells in a Notch1-induced leukemia model

机译:造血和干细胞:Notch1诱导的白血病模型中正常造血干细胞和祖细胞的动力学

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摘要

The predominant outgrowth of malignant cells over their normal counterparts in a given tissue is a shared feature for all types of cancer. However, the impact of a cancer environment on normal tissue stem and progenitor cells has not been thoroughly investigated. We began to address this important issue by studying the kinetics and functions of hematopoietic stem and progenitor cells in mice with Notch1-induced leukemia. Although hematopoiesis was progressively suppressed during leukemia development, the leukemic environment imposed distinct effects on hematopoietic stem and progenitor cells, thereby resulting in different outcomes. The normal hematopoietic stem cells in leukemic mice were kept in a more quiescent state but remained highly functional on transplantation to nonleukemic recipients. In contrast, the normal hematopoietic progenitor cells in leukemic mice demonstrated accelerated proliferation and exhaustion. Subsequent analyses on multiple cell-cycle parameters and known regulators (such as p21, p27, and p18) further support this paradigm. Therefore, our current study provides definitive evidence and plausible underlying mechanisms for hematopoietic disruption but reversible inhibition of normal hematopoietic stem cells in a leukemic environment. It may also have important implications for cancer prevention and treatment in general.
机译:在所有给定类型的组织中,恶性细胞的过度生长超过其正常对应物是所有类型癌症的共同特征。但是,尚未彻底研究癌症环境对正常组织干细胞和祖细胞的影响。我们开始通过研究Notch1诱导的白血病小鼠的造血干细胞和祖细胞的动力学和功能来解决这一重要问题。尽管在白血病的发展过程中逐渐抑制了造血功能,但白血病环境对造血干细胞和祖细胞产生了明显的影响,从而导致了不同的结果。白血病小鼠中的正常造血干细胞保持更静止的状态,但在移植给非白血病受体后仍保持高度功能。相反,白血病小鼠中的正常造血祖细胞表现出加速的增殖和衰竭。随后对多个细胞周期参数和已知调节因子(例如p21,p27和p18)的分析进一步支持了该范例。因此,我们目前的研究为白血病环境中的造血干细胞的破坏提供了明确的证据和合理的潜在机制,但可逆性抑制了正常造血干细胞。一般而言,它也可能对癌症的预防和治疗具有重要意义。

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