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重新审视干细胞可塑性:连续骨髓模型和微泡介导的表型变化。

Stem cell plasticity revisited: the continuum marrow model and phenotypic changes mediated by microvesicles.

机构信息

Division of Hematology and Oncology, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.

出版信息

Exp Hematol. 2010 Jul;38(7):581-92. doi: 10.1016/j.exphem.2010.03.021. Epub 2010 Apr 9.

Abstract

The phenotype of marrow hematopoietic stem cells is determined by cell-cycle state and microvesicle entry into the stem cells. The stem cell population is continually changing based on cell-cycle transit and can only be defined on a population basis. Purification of marrow stem cells only addresses the heterogeneity of these populations. When whole marrow is studied, the long-term repopulating stem cells are in active cell cycle. However, with some variability, when highly purified stem cells are studied, the cells appear to be dormant. Thus, the study of purified stem cells is intrinsically misleading. Tissue-derived microvesicles enhanced by injury effect the phenotype of different cell classes. We propose that previously described stem cell plasticity is due to microvesicle modulation. We further propose a stem cell population model in which the individual cell phenotypes continually change, but the population phenotype is relatively stable. This, in turn, is modulated by microvesicle and microenvironmental influences.

摘要

骨髓造血干细胞的表型由细胞周期状态和微囊泡进入干细胞决定。基于细胞周期转运,干细胞群体不断变化,只能基于群体进行定义。骨髓干细胞的纯化仅解决了这些群体的异质性问题。当研究整个骨髓时,长期重建造血干细胞处于活跃的细胞周期中。然而,具有一定的可变性,当研究高度纯化的干细胞时,细胞似乎处于休眠状态。因此,对纯化干细胞的研究本质上具有误导性。损伤增强的组织衍生微囊泡影响不同细胞类别的表型。我们提出,先前描述的干细胞可塑性是由于微囊泡的调节。我们进一步提出了一个干细胞群体模型,其中单个细胞表型不断变化,但群体表型相对稳定。这反过来又受到微囊泡和微环境影响的调节。

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