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低铁血症状态下成红细胞增殖的动力学

Kinetics of erythroblast proliferation in states of hypoferremia.

作者信息

Dörmer P, Lau B

出版信息

Isr J Med Sci. 1978 Nov;14(11):1144-51.

PMID:750541
Abstract

By application of the method of quantitative 14C-autoradiography, the kinetics of erythroblast proliferation were studied in seven patients with iron-deficiency anemia (IDA), in five cases of anemia associated with infection or malignancy (ACD), and in two patients with bleeding anemia (BLA). The turnover rate of erythroblasts was significantly reduced in IDA and ACD, and was normal in BLA. Proliferation and maturation of erythroblasts in IDA and ACD were increasingly slowed down with advancing development into mature cells. Neither changes in the number of cell divisions nor ineffective erythropoiesis were observed within the proliferative compartments. The kinetic impairments found in IDA and ACD could readily be counterbalanced by a twofold increase in the rate of stem cell differentiation. Within recognizable erythropoiesis, no compensatory effort was detectable, not even in proerythroblasts. Insufficient compensation at the stem cell level is therefore regarded as the prime lesion in IDA and ACD.

摘要

通过应用定量¹⁴C放射自显影法,对7例缺铁性贫血(IDA)患者、5例感染或恶性肿瘤相关性贫血(ACD)患者以及2例失血性贫血(BLA)患者的成红细胞增殖动力学进行了研究。IDA和ACD患者成红细胞的周转率显著降低,而BLA患者的周转率正常。随着成红细胞发育为成熟细胞,IDA和ACD患者成红细胞的增殖和成熟逐渐减缓。在增殖区室内未观察到细胞分裂数量的变化或无效红细胞生成。IDA和ACD中发现的动力学损伤可通过干细胞分化速率增加两倍而轻易得到平衡。在可识别的红细胞生成过程中,即使在早幼红细胞中也未检测到代偿性努力。因此,干细胞水平的代偿不足被认为是IDA和ACD的主要病变。

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