首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Number and continuous proliferative pattern of transplanted primitive immunohematopoietic stem cells.
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Number and continuous proliferative pattern of transplanted primitive immunohematopoietic stem cells.

机译:原始免疫造血干细胞移植的数量和连续增殖模式。

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摘要

We estimated numbers of transplantable primitive stem cells (PSCs) and found evidence that the same PSC continuously produced circulating erythrocytes and lymphocytes. These estimations used the binomial formula on data from recipients of identical portions of marrow mixtures containing two distinguishable cell types. Analysis of variance was used to compare repeated tests within each recipient. Values of pi s or pi c, probabilities that two independently sampled cells were descended from the same PSC, were also estimated, as this does not require the unverified condition that all PSCs contribute equally to the differentiated cell population. Several months after transplantation, erythrocytes were descended from only a single PSC per 1-2 X 10(5) marrow cells injected, several times rarer than previously reported. Percentages of erythrocyte and lymphocyte types in each recipient were closely correlated, with r values ranging from 0.86 to 0.94, in groups receiving 2-8 X 10(5) marrow cells; apparently the same precursors repopulated both myeloid and lymphoid lines in each recipient, as expected of true PSCs. Our data did not fit the clonal succession model, which predicts sequential activation of new PSCs and deactivation of old. Between 76 and 154 days, differentiated erythrocyte precursors were probably exhausted, with no evidence for new precursor activation or for further change between 154 and 250 days. The percentage of newly produced erythrocytes (reticulocytes) of each donor type varied little when individual recipients were followed between 165 and 295 days after transplantation, and variances within recipients were similar at marrow doses from 8 to 200 X 10(5) cells, further contradicting models of sequential activation and deactivation of PSC clones. Thus, transplanted PSCs were continually active during much of the recipient's lifespan.
机译:我们估计了可移植原始干细胞(PSC)的数量,并发现证据表明同一PSC持续产生循环性红细胞和淋巴细胞。这些估计对包含两种可区分细胞类型的骨髓混合物相同部分的接受者的数据使用了二项式公式。方差分析用于比较每个接受者内的重复测试。还估计了pi或pi c的值,即两个独立采样的细胞来自同一PSC的概率,因为这不需要所有PSC均等地参与分化的细胞群的未经验证的条件。移植后的几个月,每注射1-2 X 10(5)骨髓细胞,红细胞仅来自单个PSC,比以前报道的少了几倍。在接受2-8 X 10(5)骨髓细胞的组中,每个接受者中红细胞和淋巴细胞类型的百分比紧密相关,r值在0.86至0.94之间。显然,正如真正的PSC所期望的那样,每个接受者的髓系和淋巴系都重现了相同的前体。我们的数据不适合克隆继承模型,该模型预测了新PSC的顺序激活和旧PSC的失活。在76至154天之间,分化的红细胞前体可能已耗尽,没有证据表明新的前体激活或在154至250天之间有进一步变化。移植后165至295天之间追踪单个受体时,每种供体类型的新产生的红细胞(网状细胞)的百分比变化不大,并且骨髓剂量从8到200 X 10(5)细胞时,受体内部的差异相似。 PSC克隆的顺序激活和去激活模型。因此,移植的PSC在接受者的大部分生命中都持续活跃。

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