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促红细胞生成素或溶血性贫血诱导的干细胞迁移:促红细胞生成素制剂中放线菌素和内毒素污染的影响。

Stem cell migration induced by erythropoietin or haemolytic anaemia: the effects of actinomycin and endotoxin contamination of erythropoietin preparations.

作者信息

Quesenberry P, Levin J, Zuckerman K, Rencricca N, Sullivan R, Tyler W

出版信息

Br J Haematol. 1979 Feb;41(2):253-69. doi: 10.1111/j.1365-2141.1979.tb05854.x.

Abstract

The injection of erythropoietin or the induction of anaemia with phenylhydrazine leads to changes in murine pluripotent and granulocyte-macrophage stem cells indicating migration from marrow to spleen. In order to evaluate the interrelationship between erythroid differentiation and stem cell migration we have selectively suppressed erythroid differentiation with actinomycin D. Anaemia or EP injection resulted in stem cell changes consistent with migration; actinomycin blocked these changes in anaemic but not EP injected mice while blocking erythropoiesis in both groups. The erythropoietin contained from 0.01 to 1000 microgram/ml of endotoxin as defined by the limulus test; it decreased marrow erythropoiesis and stimulated marrow granulopoiesis. Adsorption of the erythropoietin preparation with limulus lysate removed endotoxin without decreasing erythropoietin activity. Adsorbed erythropoietin stimulated erythropoiesis and not granulopoiesis, and stem cell changes induced by its administration were largely blocked by actinomycin, suggesting that endotoxin in the non-adsorbed erythropoietin caused the actinomycin resistant stem cell changes. The observation that actinomycin blocks both erythroid differentiation and stem cell migration suggests that these two physiologic events are closely linked. The effects of injected erythropoietin on murine haemopoietic stem cells may, to a significant extent, be secondary to the presence of endotoxin in the erythropoietin preparations.

摘要

注射促红细胞生成素或用苯肼诱导贫血会导致小鼠多能干细胞和粒细胞-巨噬细胞干细胞发生变化,表明这些干细胞从骨髓迁移至脾脏。为了评估红系分化与干细胞迁移之间的相互关系,我们用放线菌素D选择性地抑制了红系分化。贫血或注射促红细胞生成素会导致干细胞发生与迁移一致的变化;放线菌素阻断了贫血小鼠的这些变化,但未阻断注射促红细胞生成素小鼠的变化,不过两组的红细胞生成均被阻断。通过鲎试剂检测,促红细胞生成素中含有0.01至1000微克/毫升的内毒素;它会减少骨髓红细胞生成并刺激骨髓粒细胞生成。用鲎试剂溶解物吸附促红细胞生成素制剂可去除内毒素,且不会降低促红细胞生成素的活性。吸附后的促红细胞生成素刺激红细胞生成而非粒细胞生成,并且其给药诱导的干细胞变化在很大程度上被放线菌素阻断,这表明未吸附的促红细胞生成素中的内毒素导致了对放线菌素耐药的干细胞变化。放线菌素同时阻断红系分化和干细胞迁移这一观察结果表明,这两个生理事件紧密相连。注射促红细胞生成素对小鼠造血干细胞的影响在很大程度上可能继发于促红细胞生成素制剂中内毒素的存在。

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