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一种用于测量小鼠造血干细胞残余损伤的检测方法。

An assay for the measurement of residual damage of murine hematopoietic stem cells.

作者信息

Häubner G E, Wangenheim K H, Feinendegen L E

出版信息

Exp Hematol. 1981 Feb;9(2):111-7.

PMID:7016563
Abstract

The proliferation rate of murine hematopoietic cells in regenerating spleen was assayed by a novel technique that analyzes the integrity of stem cells irrespective of their number. It relies on the increment of incorporation of 5-(125I) iodo-2'-deoxyuridine (125IUdR) at day 3 and 5 after transfusion of syngeneic marrow cells in fatally irradiated recipients. A prerequisite of the assay is the linearity between in fatally irradiated recipients. A prerequisite of the assay in the linearity between 125IUdR incorporation in the spleen and the number of cells transfused at both days of observation. The average increment of activity of 125IUdR from day 3 to 5 for the various graft size permits the description of a proliferation factor and from that a doubling time of the proliferating population in the spleen. Whole-body gamma-irradiation of donor mice causes a significant increase of doubling time in the grafts which persisted in part for 7 months after recovery from 500 rad exposure. The prolongation of doubling time expresses a residual injury and may interfere with the regulation of proliferation.

摘要

通过一种新技术测定再生脾脏中鼠造血细胞的增殖率,该技术可分析干细胞的完整性,而不考虑其数量。它依赖于在致死性照射的受体中输入同基因骨髓细胞后第3天和第5天5-(125I)碘-2'-脱氧尿苷(125IUdR)掺入量的增加。该测定的一个前提是在致死性照射的受体中,在观察的两天中,脾脏中125IUdR掺入量与输入细胞数量之间呈线性关系。不同移植规模下125IUdR活性从第3天到第5天的平均增加量可用于描述增殖因子,并由此得出脾脏中增殖群体的倍增时间。供体小鼠的全身γ射线照射导致移植体中倍增时间显著增加,在从500拉德照射恢复后,部分增加持续7个月。倍增时间的延长表示存在残留损伤,可能会干扰增殖调节。

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