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红细胞应激期间小鼠次要血红蛋白增加:一种血红蛋白调节模型。

Increased mouse minor hemoglobin during erythroid stress: a model for hemoglobin regulation.

作者信息

Alter B P, Campbell A S, Holland J G, Friend C

出版信息

Exp Hematol. 1982 Oct;10(9):754-60.

PMID:6959822
Abstract

In mice with "diffuse" hemoglobin (Hb), the decrease in the proportion of minor Hb during ontogeny qualitatively resembles the decline observed in human Hb F. Since Hb F reappears during some forms of erythroid stress, we investigated the effect of hematopoietic stress on minor Hb in DBA/2 mice. The stresses were acetlyphenylhydrazine-induced hemolysis, phlebotomy, or infection with Friend erythroleukemia virus. Recovery from anemia was associated with a transient increase in the synthesis of minor Hb similar to the reappearance of Hb F in man. Minor Hb synthesis also increased during the evolution of erythroleukemia induced by both the anemic and the polycythemic strains of virus. Thus, the mouse model can be used to study Hb regulation, since changes in the modulation of minor Hb synthesis occur under conditions which are associated with alterations in Hb F synthesis in humans.

摘要

在具有“弥散性”血红蛋白(Hb)的小鼠中,个体发育过程中次要Hb比例的降低在质量上类似于人类胎儿血红蛋白(Hb F)中观察到的下降。由于Hb F在某些形式的红细胞应激期间会重新出现,我们研究了造血应激对DBA/2小鼠次要Hb的影响。应激因素包括乙酰苯肼诱导的溶血、放血或感染Friend红细胞白血病病毒。从贫血中恢复与次要Hb合成的短暂增加有关,类似于人类中Hb F的重新出现。在贫血和多血症病毒株诱导的红细胞白血病演变过程中,次要Hb合成也增加。因此,该小鼠模型可用于研究Hb调节,因为次要Hb合成调节的变化发生在与人类Hb F合成改变相关的条件下。

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