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Hematopoiesis and Stem Cells: Impact of interactions of cellular components of the bone marrow microenvironment on hematopoietic stem and progenitor cell function

机译:造血和干细胞:骨髓微环境的细胞成分相互作用对造血干细胞和祖细胞功能的影响

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摘要

Hematopoietic stem (HSC) and progenitor (HPC) cell fate is governed by intrinsic and extrinsic parameters. We examined the impact of hematopoietic niche elements on HSC and HPC function by analyzing the combined effect of osteoblasts (OBs) and stromal cells (SCs) on LineageSca-1+CD117+ (LSK) cells. CFU expansion and marrow repopulating potential of cultured LineageSca-1+CD117+ cells were significantly higher in OB compared with SC cultures, thus corroborating the importance of OBs in the competence of the hematopoietic niche. OB-mediated enhancement of HSC and HPC function was reduced in cocultures of OBs and SCs, suggesting that SCs suppressed the OB-mediated hematopoiesis-enhancing activity. Although the suppressive effect of SC was mediated by adipocytes, probably through up-regulation of neuropilin-1, the OB-mediated enhanced hematopoiesis function was elaborated through Notch signaling. Expression of Notch 2, Jagged 1 and 2, Delta 1 and 4, Hes 1 and 5, and Deltex was increased in OB cultures and suppressed in SC and OB/SC cultures. Phenotypic fractionation of OBs did not segregate the hematopoiesis-enhancing activity but demonstrated that this function is common to OBs from different anatomic sites. These data illustrate that OBs promote in vitro maintenance of hematopoietic functions, including repopulating potential by up-regulating Notch-mediated signaling between HSCs and OBs.
机译:造血干细胞(HSC)和祖细胞(HPC)的命运受内在和外在参数控制。通过分析成骨细胞(OBs)和基质细胞(SCs)对沿袭- Sca-1 + 的联合作用,我们检查了造血环境元素对HSC和HPC功能的影响CD117 + (LSK)细胞。与SC培养相比,培养的谱系- Sca-1 + CD117 + 细胞的CFU扩增和骨髓再增殖潜力明显高于SC培养,从而证实了这一点。 OB在造血生境能力中的重要性。在OB和SC的共培养中,OB介导的HSC和HPC功能的增强降低,表明SC抑制了OB介导的造血功能增强活性。尽管SC的抑制作用是由脂肪细胞介导的,但可能是通过neuropilin-1的上调来实现的,但通过Notch信号可详细阐明OB介导的增强的造血功能。 Notch 2,锯齿1和2,Delta 1和4,Hes 1和5以及Deltex的表达在OB培养物中增加,而在SC和OB / SC培养物中则受到抑制。 OB的表型分级分离并未分离出增强造血作用的活性,但证明了该功能对于不同解剖部位的OB是共有的。这些数据表明,OB促进了造血功能的体外维持,包括通过上调HSC和OB之间的Notch介导的信号传导来重新发挥潜力。

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