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Secreted frizzled-related protein 1 extrinsically regulates cycling activity and maintenance of hematopoietic stem cells.

机译:分泌的卷曲相关蛋白1外在调节循环活动和造血干细胞的维持。

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摘要

Secreted frizzled-related protein 1 (Sfrp1) is highly expressed by stromal cells maintaining hematopoietic stem cells (HSCs). Sfrp1 loss in stromal cells increases production of hematopoietic progenitors, and in knockout mice, dysregulates hemostasis and increases Flk2- Cd34- Lin- Sca1+ Kit+ (LSK) cell numbers in bone marrow. Also, LSK and multipotent progenitors (MPPs) resided mainly in the G0/G1 phase of cell cycle, with an accompanying decrease in intracellular beta-catenin levels. Gene-expression studies showed a concomitant decrease Ccnd1 and Dkk1 in Cd34- LSK cells and increased expression of Pparg, Hes1, and Runx1 in MPP. Transplantation experiments showed no intrinsic effect of Sfrp1 loss on the number of HSCs or their ability to engraft irradiated recipients. In contrast, serial transplantations of wild-type HSCs into Sfrp1(-/-) mice show a progressive decrease of wild-type LSK and MPP numbers. Our results demonstrate that Sfrp1 is required to maintain HSC homeostasis through extrinsic regulation of beta-catenin.
机译:分泌的卷曲相关蛋白1(Sfrp1)由维持造血干细胞(HSC)的基质细胞高表达。 Sfrp1在基质细胞中的丢失会增加造血祖细胞的产生,而在敲除小鼠中则会失调止血,并增加骨髓中Flk2-Cd34-Lin-Sca1 + Kit +(LSK)细胞的数量。同样,LSK和多能祖细胞(MPPs)主要存在于细胞周期的G0 / G1期,伴随着细胞内β-catenin水平的降低。基因表达研究表明,Cd34-LSK细胞中Ccnd1和Dkk1减少,MPP中Pparg,Hes1和Runx1的表达增加。移植实验表明,Sfrp1丢失对HSC的数量或其移植受辐照受体的能力没有内在影响。相比之下,野生型HSC到Sfrp1(-/-)小鼠的系列移植显示出野生型LSK和MPP数量的逐渐减少。我们的结果表明,Sfrp1是通过β-catenin的外在调节来维持HSC稳态所必需的。

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