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源自配对祖细胞的小鼠造血集落中的不同分化

Disparate differentiation in mouse hemopoietic colonies derived from paired progenitors.

作者信息

Suda T, Suda J, Ogawa M

出版信息

Proc Natl Acad Sci U S A. 1984 Apr;81(8):2520-4. doi: 10.1073/pnas.81.8.2520.

Abstract

We analyzed the differentiation of murine hemopoietic colonies derived from paired progenitors in culture. Single progenitors were isolated by use of a micromanipulation technique from blast cell colonies cultured from the spleens of 5-fluorouracil-treated mice. Eighteen to 24 hr later, the paired progenitors were separated with a micromanipulator and cultured in methylcellulose medium containing erythropoietin and pokeweed-mitogen spleen cell conditioned medium. Six to nine days later, the two colonies derived from the paired progenitors were individually picked and differential counts were performed by using May-Grunwald-Giemsa stain. The abbreviations used here are n, neutrophil; m, macrophage; e, eosinophil; mast, mast cell; M, megakaryocyte; E, erythrocyte. Of a total of 387 pairs that could be evaluated, 68 were pairs of colonies consisting of dissimilar combinations of cell lineages such as m-nmmastEM, M-nmmastEM, nm-nmmastEM, nmmastM-nmmastEM, M-nmmastM, nmmast-nmmastM, nm-nmmastE, M-nmM, n-nmM, mM-nmM, m-nmmast, nm-nme, me-nm, mM-nm, n-ne, m-mmast, m-mM, M-nm, M-mM, E-nm, m-nm, M-m, etc. Thirty-nine were homologous pairs revealing identical lineage combinations such as nmmastEM, nmmastM, nmmast, mmastEM, nmEM, nme, nmM, mM, and nm lineages. However, in members of some of these pairs, the proportions of the individual cell lineages were significantly different. The remainder were pairs of single lineage colonies. Paired progenitors obtained from the stem cell colonies of normal mice also revealed homologous and nonhomologous expression of the cell lineages. Comparison of lineage expression in colonies derived from single progenitors with the sum of lineages expressed in pairs of colonies derived from single progenitors indicated that the diversity was not due to injury inflicted by micromanipulation. These observations provide experimental data in support of stochastic mechanisms of stem cell differentiation.

摘要

我们分析了培养中源自配对祖细胞的小鼠造血集落的分化情况。通过显微操作技术从5-氟尿嘧啶处理小鼠脾脏培养的原始细胞集落中分离出单个祖细胞。18至24小时后,用显微操作器分离配对祖细胞,并在含有促红细胞生成素和商陆有丝分裂原脾细胞条件培养基的甲基纤维素培养基中培养。6至9天后,分别挑选源自配对祖细胞的两个集落,并使用May-Grunwald-Giemsa染色进行细胞分类计数。这里使用的缩写为:n,中性粒细胞;m,巨噬细胞;e,嗜酸性粒细胞;mast,肥大细胞;M,巨核细胞;E,红细胞。在总共387对可评估的配对中,68对是由不同细胞谱系组合组成的集落对,如m-nmmastEM、M-nmmastEM、nm-nmmastEM、nmmastM-nmmastEM、M-nmmastM、nmmast-nmmastM、nm-nmmastE、M-nmM、n-nmM、mM-nmM、m-nmmast、nm-nme、me-nm、mM-nm、n-ne、m-mmast、m-mM、M-nm、M-mM、E-nm、m-nm、M-m等。39对是同源对,显示相同的谱系组合,如nmmastEM、nmmastM、nmmast、mmastEM、nmEM、nme、nmM、mM和nm谱系。然而,在其中一些配对的成员中,各个细胞谱系的比例存在显著差异。其余的是单谱系集落对。从正常小鼠干细胞集落获得的配对祖细胞也显示出细胞谱系的同源和非同源表达。将源自单个祖细胞的集落中的谱系表达与源自单个祖细胞的配对集落中表达的谱系总和进行比较,表明这种多样性并非由显微操作造成的损伤所致。这些观察结果提供了支持干细胞分化随机机制的实验数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e35/345094/8622d0a286ab/pnas00609-0254-a.jpg

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